Senior Clinical Research Associate / Clinical Research Associate II - Oncology - West Coast US - FSP
Oncology - West Coast US - FSP · Atlas, Michigan, United States
Full-time
Posted Sep 1, 2026
Job Description
ATLAS MEDICAL SERVICES LTD. STI.
United States
Full-time Posted Aug 31, 2026
Job Description
My research opens up
new medical possibilities.
And I do it
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Senior Clinical Research Associate / Clinical Research Associate II - Oncology - West Coast US - FSP
Primary Location: United States, Remote Additional Locations: United States, Oregon, Remote; United States, Washington, Remote Job ID R0000044755 Category Clinical Trials Date Posted 08/18/2026
Apply Now
Success profile
About This Role
Potential career path
Employee insights
Our team
Why Clinical Research Associates work at Parexel
Learn about our culture
Overview
As a Clinical Research Associate (CRA) at Parexel, you act as an integral part to get treatments to patients sooner. Our CRAs' priority is the safety and well-being of the patients. As you travel to investigator sites and perform your monitoring duties, we encourage you to be inquisitive, take accountability, build relationships, and act with integrity.
Join a team with a wide variety of experiences and knowledge, and work on global projects within a broad scope of therapeutic areas. We’re looking for people who want to grow personally and professionally and support their colleagues globally and cross-functionally.
Success Profile
Do you have these soft skills and interpersonal traits to succeed at Parexel?
Communicator
Detail-oriented
Flexible
Organized
Problem-solver
Self-starter
Back to nav
About This Role
Parexel is seeking a Senior Clinical Research Associate or Clinical Research Associate II who is experienced in Oncology On-Site Monitoring on the West Coast, US!
Job Purpose
The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices (GCP), and sponsor standards. The Sr. CRA is accountable for site management and monitoring, managing investigator site relationships to ensure effective delivery of clinical trials (e.g. enrollment, database release), to safeguard the quality of investigator sites (e.g. patient safety, site quality and compliance with GCP), to maintain investigator and site staff engagement and satisfaction, and to enhance the company’s image with its external stakeholders. The Sr. CRA is responsible for the resolution of all protocol-related issues for assigned investigator sites and will work closely with the Site Care Partner (SCP), and other members of the study team, as required, in activities associated with the set-up, running and close-out of sites in a clinical trial.
Key Accountabilities
Oversight of Monitoring Responsibilities and Study Conduct
Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and sponsor standards to achieve project goals, timelines and quality
Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to database lock, ensuring relevant timelines and quality deliverables are met
During study conduct, serve as the primary point of contact for assigned investigator sites. Work in partnership with and/or escalate to the SCP to ensure quality of site delivery
Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites
Partner with SCP to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients; provide protocol training to, and address protocol related questions from the investigator site staff when required, including discussions on known/anticipated operational and clinical trial risks
Attend investigator meeting when required (virtual or F2F). Provide enrollment support and ensure progress by responding to site activation and
recruitment issues from investigators. Partner with SCP and the study team to define and support recruitment initiatives at site level
Conduct onsite, remote/electronic monitoring as needed for study site initiation, routine monitoring and study site closure activities and ensure these are conducted accordance to the SMP, Standard Operating Procedures (SOPs) and commensurate with emerging issues and technologies
Monitor site level adverse events (AEs) and serious adverse events (SAEs) and collaborate with the Drug Safety Unit and follow-up with investigators sites, as needed, to bring SAE reports required information to resolution
Submit all required reports, documentation, updates and tracking within required timeframes, including but not limited to Trial Master File (TMF) documentation, site reports, site follow up letters, protocol deviations, patient recruitment, clinical supply management, study progress and metrics
Identify and resolve investigator site issues within required timeframes; agree and develop corrective and preventative actions with investigator and site personnel to close open issues and to prevent recurrence/persistence of issues
Resolve data queries within required timelines, prepare investigator site close-out plan and conduct close-out activities within required timelines
Ensures adequate oversight of the investigational product at the investigator site, including receipt, handling, accounting, storage conditions, and destruction activities
Support database release as needed
May undertake the responsibilities of an unblinded monitor where appropriate
Clinical/Scientific and Site Monitoring Risk
Maintain thorough understanding of the product, protocol and therapy area in sufficient details to have appropriate discussions with the investigator and site team
Interact with investigator site heath care professionals in a manner which enhances sponsor’s credibility, scientific leadership and in order to facilitate sponsor’s clinical development goals
Support the study clinician in ensuring patient safety, eligibility and providing clinical guidance to investigators
Drive Quality Event (QE) remediation, when applicable
Serve as a point of contact for audit conduct, and drive Audit Observation corrective action/preventive action (CAPA) development and checks, when applicable
Collaboration
Reports to Director of Clinical Site Operations (DCSO) or Director of Site Management and Monitoring (DSMM)
Partners with SCP and Country Study Operations Manager (SOM)
When required Partners with other Study Team members (e.g. Clinician, Recruitment Specialist, Clinical Data Scientist)
May act as a Mentor for Clinical Research Associates
Skills
Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology) in a CRO or pharma organization
Preferred Therapeutic Experience In Oncology
Global clinical trial experience preferred
Extensive knowledge of clinical trial methodologies, ICH/GCP, Food and Drug Administration (FDA) and local country regulations
Must be fluent in English and in the native language(s) of the country they will work in
Travel within area is required
Valid driver’s license and passport required
Knowledge And Experience
Demonstrated knowledge of clinical research and development processes and ability to gain command of process details
Demonstrated knowledge of global and local regulatory requirements
Demonstrated understanding of key operational elements of clinical research (e.g., monitoring, data acquisition and cleaning, reporting, etc.)
Demonstrated knowledge in disease and technical areas pertaining to clinical studies, including knowledge of company direction, investigational product(s), and associated development plan(s)
Demonstrated ability to support sponsor regulatory interactions/inspections
Demonstrated knowledge of the processes around protocol design and feasibility assessment
Demonstrated understanding of region/country, culture, and medical practice and how they affect clinical trial delivery
Proven ability to work in a matrix team environment with the ability to influence, drive / lead and work through others for successful delivery of clinical trial
Ability to evaluate, interpret and present complex issues and data to support risk management and mitigation
Effective verbal and written communication skills in relating to colleagues and associates both inside and outside of the organization
Education
Bachelor’s degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical is required
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the United States includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
Back to nav
Share this job
LinkedIn
Facebook
X
Email
Potential Career Path
Parexel offers various career paths and internal development programs for CRAs to advance to the next level. This could include enhancing your technical position, moving into management, or shifting to other areas of the business.
APEX CRA
CRA I
CRA II
Senior CRA
Project Management
Subject Matter Expert
People Management
Back to nav
Employee Insights
Nick on a day in the life of a CRA
Nick Burger | Senior Clinical Research Associate
Watch Video
Liliana on CRA tasks and our recognition program
Liliana Belmares Flores | CRA Line Manager
Watch Video
Marlayna on why Parexel is a great place for CRAs
Marlayna Fitts | CRA Line Manager
Watch Video
Back to nav
TEAM IMPRESSIONS
Back to nav
Why Clinical Research Associates work at Parexel
Patient-focused in everything we do
We push the boundaries of what is possible to create clinical trials that are inclusive, innovative, and patient-focused
Supportive and inclusive environment
We foster collaboration, teamwork, respect, and inclusivity, to work together to achieve common goals.
Career growth and development
We develop your skills through training, mentorship, and career advancement programs.
Flexible work arrangements
We focus on outputs and results, not where and when you work.
Diverse therapeutic areas and project exposure
We continuously learn from a broad exposure from early to late phase clinical trials and our cros-functional global teams.
Advanced Technology
We recognize the importance of first-time quality to bring treatments to patients faster.
Back to nav
Learn About Our Culture
Back to nav
Back to nav
Meet Hina, an Executive Director championing excellence and empathy
Parexel's Hina Saleem, Executive Director, Clinical Operations, shares how empathy and excellence drive her approach to clinical trial optimization and authentic leadership.
Learn More
Meet Julie, a Senior Clinical Assistant, proud of her contribution
Julie welcomes volunteers at the Early Phase Clinic reception in Berlin, manages payments, and caters to the volunteers in the kitchen.
Learn More
Meet Adriane, a Senior Clinical Operations Leader sharing insights and tips
Discover Adriane's role as a Clinical Operations Leader. She shares insights into her daily responsibilities, the skills crucial for success, and the rewarding challenges she faces. Learn how Parexel supported her career development and gain inspiration from her advice on professional growth.
Learn More
Working as a Nurse in Clinical Research at Parexel
Antje and Katharina share insights into working as a Nurse in Clinical Research, where innovative medications are developed through early-phase and first-in-human studies.
Learn More
Meet David, a champion for disability inclusion
His leadership fosters workplace and clinical research inclusivity. Explore David's inspiring journey from combat medic to Parexel VP and Disability Inclusion Business Resource Group co-lead.
Learn More
Meet Margaret: Clinical Research Nurse
Find out why Margaret enjoys working as a Nurse in Clinical Research and working at Parexel, also how Parexel supports her in a way she hasn't experienced anywhere else.
Learn More
Clinical Operations Opportunities
Are you passionate about making a difference in the fight against cancer and beyond? At Parexel's Global Clinical Operations, we are dedicated to putting patients at the heart of every clinical trial. With a global footprint and 5000 Clinical Operations team members worldwide, we are impacting clinical research.
Learn More
Meet Laurias: Manager, Clinical Operations
Laurias shares how Parexel has supported his career development from CRA to Clin Ops Manager and flexibility within the workplace.
Learn More
Meet Stacy Hurt, Chief Patient Officer at Parexel
Insights on Parexel's patient-centric approach, innovative strategies, and authentic culture in clinical research. Learn how Stacy's unique experiences shape the future of clinical trials.
Learn More
Optimizing the clinical research workforce: An industry analysis by Parexel
This comprehensive report benchmarks the trends and innovations having the greatest impact on drug development and identifies the skills required for today’s workforce.
Learn More
Meet iCRA Twins Marina Palumbo and Anna Korelis
Double the passion and double the commitment to working With Heart™. Read on to learn more about these colleagues whose family and work lives are uniquely intertwined at Parexel!
Learn More
Video on Working With Heart® - Christina's Clinical Operations Manager Perspective
View how Christina reflects on her work experience, her impact on patients and her management style of respect and growth. Christina is leading a team of Clinical Operations Leaders who manage groundbreaking trials in the biotech space.
Learn More
Meet Andrea: Senior Initiation Clinical Research Associate
Andrea's story shows how teamwork, attention to detail and patient focus drive success at Parexel while finding fulfillment in helping innovative treatments reach patients faster.
Learn More
Meet Alexis, a Clinical Research Associate II championing patient care
Alexis progressed from Administrative Assistant to CRA via Parexel's APEX program. She passionately works for the patients, sites and coworkers to make a difference. Off-duty, she enjoys time with her poodle, Millie, and baking shows.
Learn More
Emerging Talent Opportunities
Begin your career journey at Parexel with our emerging talent programs or our internships, placements and entry-level clinical roles. Advance science by keeping the patients in mind.
Learn More
Inclusion at Parexel
Learn how Parexel celebrates the differences our workforce and patients bring and ensures an inclusive environment.
Learn More
Benefits & Support
At Parexel, we prioritize putting people first, allowing you to achieve your best work. Explore the Flexible Work Program, our "Bravo" Recognition Program, and how we build our well-being in our supportive culture.
Learn More
Apply Now
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My research opens up
new medical possibilities.
And I do it
Search Jobs
Search Jobs
Keyword
Matching job links will appear below as you type.
Location: When autocomplete results are available use up and down arrows to review and enter to select. Touch device users, explore by touch or with swipe gestures.
Radius: Enter distance 5 15 25 35 50
Unit MILES KM
View Remote Jobs View All Jobs
View remote jobs View all jobs
Senior Clinical Research Associate / Clinical Research Associate II - Oncology - West Coast US - FSP
Primary Location: United States, Remote Additional Locations: United States, Oregon, Remote; United States, Washington, Remote Job ID R0000044755 Category Clinical Trials Date Posted 08/18/2026
Apply Now
Success profile
Global Clinical Trial Experience Preferred
Extensive knowledge of clinical trial methodologies, ICH/GCP, Food and Drug Administration (FDA) and local country regulations
Must be fluent in English and in the native language(s) of the country they will work in
Travel within area is required
Valid driver’s license and passport required
Knowledge And Experience
Demonstrated knowledge of clinical research and development processes and ability to gain command of process details
Demonstrated knowledge of global and local regulatory requirements
Demonstrated understanding of key operational elements of clinical research (e.g., monitoring, data acquisition and cleaning, reporting, etc.)
Demonstrated knowledge in disease and technical areas pertaining to clinical studies, including knowledge of company direction, investigational product(s), and associated development plan(s)
Demonstrated ability to support sponsor regulatory interactions/inspections
Demonstrated knowledge of the processes around protocol design and feasibility assessment
Demonstrated understanding of region/country, culture, and medical practice and how they affect clinical trial delivery
Proven ability to work in a matrix team environment with the ability to influence, drive / lead and work through others for successful delivery of clinical trial
Ability to evaluate, interpret and present complex issues and data to support risk management and mitigation
Effective verbal and written communication skills in relating to colleagues and associates both inside and outside of the organization
Education
Bachelor’s degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical is required
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the United States includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
Back to nav
Share this job
LinkedIn
Facebook
X
Email
Potential Career Path
Parexel offers various career paths and internal development programs for CRAs to advance to the next level. This could include enhancing your technical position, moving into management, or shifting to other areas of the business.
APEX CRA
CRA I
CRA II
Senior CRA
Project Management
Subject Matter Expert
People Management
Back to nav
Employee Insights
Nick on a day in the life of a CRA
Nick Burger | Senior Clinical Research Associate
Watch Video
Liliana on CRA tasks and our recognition program
Liliana Belmares Flores | CRA Line Manager
Watch Video
Marlayna on why Parexel is a great place for CRAs
Marlayna Fitts | CRA Line Manager
Watch Video
Back to nav
TEAM IMPRESSIONS
Back to nav
Why Clinical Research Associates work at Parexel
Patient-focused in everything we do
We push the boundaries of what is possible to create clinical trials that are inclusive, innovative, and patient-focused
Supportive and inclusive environment
We foster collaboration, teamwork, respect, and inclusivity, to work together to achieve common goals.
Career growth and development
We develop your skills through training, mentorship, and career advancement programs.
Flexible work arrangements
We focus on outputs and results, not where and when you work.
Diverse therapeutic areas and project exposure
We continuously learn from a broad exposure from early to late phase clinical trials and our cros-functional global teams.
Advanced Technology
We recognize the importance of first-time quality to bring treatments to patients faster.
Back to nav
Learn About Our Culture
Back to nav
Back to nav
Meet Hina, an Executive Director championing excellence and empathy
Parexel's Hina Saleem, Executive Director, Clinical Operations, shares how empathy and excellence drive her approach to clinical trial optimization and authentic leadership.
Learn More
Meet Julie, a Senior Clinical Assistant, proud of her contribution
Julie welcomes volunteers at the Early Phase Clinic reception in Berlin, manages payments, and caters to the volunteers in the kitchen.
Learn More
Meet Adriane, a Senior Clinical Operations Leader sharing insights and tips
Discover Adriane's role as a Clinical Operations Leader. She shares insights into her daily responsibilities, the skills crucial for success, and the rewarding challenges she faces. Learn how Parexel supported her career development and gain inspiration from her advice on professional growth.
Learn More
Working as a Nurse in Clinical Research at Parexel
Antje and Katharina share insights into working as a Nurse in Clinical Research, where innovative medications are developed through early-phase and first-in-human studies.
Learn More
Meet David, a champion for disability inclusion
His leadership fosters workplace and clinical research inclusivity. Explore David's inspiring journey from combat medic to Parexel VP and Disability Inclusion Business Resource Group co-lead.
Learn More
Meet Margaret: Clinical Research Nurse
Find out why Margaret enjoys working as a Nurse in Clinical Research and working at Parexel, also how Parexel supports her in a way she hasn't experienced anywhere else.
Learn More
Clinical Operations Opportunities
Are you passionate about making a difference in the fight against cancer and beyond? At Parexel's Global Clinical Operations, we are dedicated to putting patients at the heart of every clinical trial. With a global footprint and 5000 Clinical Operations team members worldwide, we are impacting clinical research.
Learn More
Meet Laurias: Manager, Clinical Operations
Laurias shares how Parexel has supported his career development from CRA to Clin Ops Manager and flexibility within the workplace.
Learn More
Meet Stacy Hurt, Chief Patient Officer at Parexel
Insights on Parexel's patient-centric approach, innovative strategies, and authentic culture in clinical research. Learn how Stacy's unique experiences shape the future of clinical trials.
Learn More
Optimizing the clinical research workforce: An industry analysis by Parexel
This comprehensive report benchmarks the trends and innovations having the greatest impact on drug development and identifies the skills required for today’s workforce.
Learn More
Meet iCRA Twins Marina Palumbo and Anna Korelis
Double the passion and double the commitment to working With Heart™. Read on to learn more about these colleagues whose family and work lives are uniquely intertwined at Parexel!
Learn More
Video on Working With Heart® - Christina's Clinical Operations Manager Perspective
View how Christina reflects on her work experience, her impact on patients and her management style of respect and growth. Christina is leading a team of Clinical Operations Leaders who manage groundbreaking trials in the biotech space.
Learn More
Meet Andrea: Senior Initiation Clinical Research Associate
Andrea's story shows how teamwork, attention to detail and patient focus drive success at Parexel while finding fulfillment in helping innovative treatments reach patients faster.
Learn More
Meet Alexis, a Clinical Research Associate II championing patient care
Alexis progressed from Administrative Assistant to CRA via Parexel's APEX program. She passionately works for the patients, sites and coworkers to make a difference. Off-duty, she enjoys time with her poodle, Millie, and baking shows.
Learn More
Emerging Talent Opportunities
Begin your career journey at Parexel with our emerging talent programs or our internships, placements and entry-level clinical roles. Advance science by keeping the patients in mind.
Learn More
Inclusion at Parexel
Learn how Parexel celebrates the differences our workforce and patients bring and ensures an inclusive environment.
Learn More
Benefits & Support
At Parexel, we prioritize putting people first, allowing you to achieve your best work. Explore the Flexible Work Program, our "Bravo" Recognition Program, and how we build our well-being in our supportive culture.
Learn More
United States
Full-time Posted Aug 31, 2026
Job Description
My research opens up
new medical possibilities.
And I do it
Search Jobs
Search Jobs
Keyword
Matching job links will appear below as you type.
Location: When autocomplete results are available use up and down arrows to review and enter to select. Touch device users, explore by touch or with swipe gestures.
Radius: Enter distance 5 15 25 35 50
Unit MILES KM
View Remote Jobs View All Jobs
View remote jobs View all jobs
Senior Clinical Research Associate / Clinical Research Associate II - Oncology - West Coast US - FSP
Primary Location: United States, Remote Additional Locations: United States, Oregon, Remote; United States, Washington, Remote Job ID R0000044755 Category Clinical Trials Date Posted 08/18/2026
Apply Now
Success profile
About This Role
Potential career path
Employee insights
Our team
Why Clinical Research Associates work at Parexel
Learn about our culture
Overview
As a Clinical Research Associate (CRA) at Parexel, you act as an integral part to get treatments to patients sooner. Our CRAs' priority is the safety and well-being of the patients. As you travel to investigator sites and perform your monitoring duties, we encourage you to be inquisitive, take accountability, build relationships, and act with integrity.
Join a team with a wide variety of experiences and knowledge, and work on global projects within a broad scope of therapeutic areas. We’re looking for people who want to grow personally and professionally and support their colleagues globally and cross-functionally.
Success Profile
Do you have these soft skills and interpersonal traits to succeed at Parexel?
Communicator
Detail-oriented
Flexible
Organized
Problem-solver
Self-starter
Back to nav
About This Role
Parexel is seeking a Senior Clinical Research Associate or Clinical Research Associate II who is experienced in Oncology On-Site Monitoring on the West Coast, US!
Job Purpose
The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality study execution in accordance with applicable prevailing laws, Good Clinical Practices (GCP), and sponsor standards. The Sr. CRA is accountable for site management and monitoring, managing investigator site relationships to ensure effective delivery of clinical trials (e.g. enrollment, database release), to safeguard the quality of investigator sites (e.g. patient safety, site quality and compliance with GCP), to maintain investigator and site staff engagement and satisfaction, and to enhance the company’s image with its external stakeholders. The Sr. CRA is responsible for the resolution of all protocol-related issues for assigned investigator sites and will work closely with the Site Care Partner (SCP), and other members of the study team, as required, in activities associated with the set-up, running and close-out of sites in a clinical trial.
Key Accountabilities
Oversight of Monitoring Responsibilities and Study Conduct
Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and sponsor standards to achieve project goals, timelines and quality
Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to database lock, ensuring relevant timelines and quality deliverables are met
During study conduct, serve as the primary point of contact for assigned investigator sites. Work in partnership with and/or escalate to the SCP to ensure quality of site delivery
Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites
Partner with SCP to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients; provide protocol training to, and address protocol related questions from the investigator site staff when required, including discussions on known/anticipated operational and clinical trial risks
Attend investigator meeting when required (virtual or F2F). Provide enrollment support and ensure progress by responding to site activation and
recruitment issues from investigators. Partner with SCP and the study team to define and support recruitment initiatives at site level
Conduct onsite, remote/electronic monitoring as needed for study site initiation, routine monitoring and study site closure activities and ensure these are conducted accordance to the SMP, Standard Operating Procedures (SOPs) and commensurate with emerging issues and technologies
Monitor site level adverse events (AEs) and serious adverse events (SAEs) and collaborate with the Drug Safety Unit and follow-up with investigators sites, as needed, to bring SAE reports required information to resolution
Submit all required reports, documentation, updates and tracking within required timeframes, including but not limited to Trial Master File (TMF) documentation, site reports, site follow up letters, protocol deviations, patient recruitment, clinical supply management, study progress and metrics
Identify and resolve investigator site issues within required timeframes; agree and develop corrective and preventative actions with investigator and site personnel to close open issues and to prevent recurrence/persistence of issues
Resolve data queries within required timelines, prepare investigator site close-out plan and conduct close-out activities within required timelines
Ensures adequate oversight of the investigational product at the investigator site, including receipt, handling, accounting, storage conditions, and destruction activities
Support database release as needed
May undertake the responsibilities of an unblinded monitor where appropriate
Clinical/Scientific and Site Monitoring Risk
Maintain thorough understanding of the product, protocol and therapy area in sufficient details to have appropriate discussions with the investigator and site team
Interact with investigator site heath care professionals in a manner which enhances sponsor’s credibility, scientific leadership and in order to facilitate sponsor’s clinical development goals
Support the study clinician in ensuring patient safety, eligibility and providing clinical guidance to investigators
Drive Quality Event (QE) remediation, when applicable
Serve as a point of contact for audit conduct, and drive Audit Observation corrective action/preventive action (CAPA) development and checks, when applicable
Collaboration
Reports to Director of Clinical Site Operations (DCSO) or Director of Site Management and Monitoring (DSMM)
Partners with SCP and Country Study Operations Manager (SOM)
When required Partners with other Study Team members (e.g. Clinician, Recruitment Specialist, Clinical Data Scientist)
May act as a Mentor for Clinical Research Associates
Skills
Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology) in a CRO or pharma organization
Preferred Therapeutic Experience In Oncology
Global clinical trial experience preferred
Extensive knowledge of clinical trial methodologies, ICH/GCP, Food and Drug Administration (FDA) and local country regulations
Must be fluent in English and in the native language(s) of the country they will work in
Travel within area is required
Valid driver’s license and passport required
Knowledge And Experience
Demonstrated knowledge of clinical research and development processes and ability to gain command of process details
Demonstrated knowledge of global and local regulatory requirements
Demonstrated understanding of key operational elements of clinical research (e.g., monitoring, data acquisition and cleaning, reporting, etc.)
Demonstrated knowledge in disease and technical areas pertaining to clinical studies, including knowledge of company direction, investigational product(s), and associated development plan(s)
Demonstrated ability to support sponsor regulatory interactions/inspections
Demonstrated knowledge of the processes around protocol design and feasibility assessment
Demonstrated understanding of region/country, culture, and medical practice and how they affect clinical trial delivery
Proven ability to work in a matrix team environment with the ability to influence, drive / lead and work through others for successful delivery of clinical trial
Ability to evaluate, interpret and present complex issues and data to support risk management and mitigation
Effective verbal and written communication skills in relating to colleagues and associates both inside and outside of the organization
Education
Bachelor’s degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical is required
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the United States includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
Back to nav
Share this job
X
Potential Career Path
Parexel offers various career paths and internal development programs for CRAs to advance to the next level. This could include enhancing your technical position, moving into management, or shifting to other areas of the business.
APEX CRA
CRA I
CRA II
Senior CRA
Project Management
Subject Matter Expert
People Management
Back to nav
Employee Insights
Nick on a day in the life of a CRA
Nick Burger | Senior Clinical Research Associate
Watch Video
Liliana on CRA tasks and our recognition program
Liliana Belmares Flores | CRA Line Manager
Watch Video
Marlayna on why Parexel is a great place for CRAs
Marlayna Fitts | CRA Line Manager
Watch Video
Back to nav
TEAM IMPRESSIONS
Back to nav
Why Clinical Research Associates work at Parexel
Patient-focused in everything we do
We push the boundaries of what is possible to create clinical trials that are inclusive, innovative, and patient-focused
Supportive and inclusive environment
We foster collaboration, teamwork, respect, and inclusivity, to work together to achieve common goals.
Career growth and development
We develop your skills through training, mentorship, and career advancement programs.
Flexible work arrangements
We focus on outputs and results, not where and when you work.
Diverse therapeutic areas and project exposure
We continuously learn from a broad exposure from early to late phase clinical trials and our cros-functional global teams.
Advanced Technology
We recognize the importance of first-time quality to bring treatments to patients faster.
Back to nav
Learn About Our Culture
Back to nav
Back to nav
Meet Hina, an Executive Director championing excellence and empathy
Parexel's Hina Saleem, Executive Director, Clinical Operations, shares how empathy and excellence drive her approach to clinical trial optimization and authentic leadership.
Learn More
Meet Julie, a Senior Clinical Assistant, proud of her contribution
Julie welcomes volunteers at the Early Phase Clinic reception in Berlin, manages payments, and caters to the volunteers in the kitchen.
Learn More
Meet Adriane, a Senior Clinical Operations Leader sharing insights and tips
Discover Adriane's role as a Clinical Operations Leader. She shares insights into her daily responsibilities, the skills crucial for success, and the rewarding challenges she faces. Learn how Parexel supported her career development and gain inspiration from her advice on professional growth.
Learn More
Working as a Nurse in Clinical Research at Parexel
Antje and Katharina share insights into working as a Nurse in Clinical Research, where innovative medications are developed through early-phase and first-in-human studies.
Learn More
Meet David, a champion for disability inclusion
His leadership fosters workplace and clinical research inclusivity. Explore David's inspiring journey from combat medic to Parexel VP and Disability Inclusion Business Resource Group co-lead.
Learn More
Meet Margaret: Clinical Research Nurse
Find out why Margaret enjoys working as a Nurse in Clinical Research and working at Parexel, also how Parexel supports her in a way she hasn't experienced anywhere else.
Learn More
Clinical Operations Opportunities
Are you passionate about making a difference in the fight against cancer and beyond? At Parexel's Global Clinical Operations, we are dedicated to putting patients at the heart of every clinical trial. With a global footprint and 5000 Clinical Operations team members worldwide, we are impacting clinical research.
Learn More
Meet Laurias: Manager, Clinical Operations
Laurias shares how Parexel has supported his career development from CRA to Clin Ops Manager and flexibility within the workplace.
Learn More
Meet Stacy Hurt, Chief Patient Officer at Parexel
Insights on Parexel's patient-centric approach, innovative strategies, and authentic culture in clinical research. Learn how Stacy's unique experiences shape the future of clinical trials.
Learn More
Optimizing the clinical research workforce: An industry analysis by Parexel
This comprehensive report benchmarks the trends and innovations having the greatest impact on drug development and identifies the skills required for today’s workforce.
Learn More
Meet iCRA Twins Marina Palumbo and Anna Korelis
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Senior Clinical Research Associate / Clinical Research Associate II - Oncology - West Coast US - FSP
Primary Location: United States, Remote Additional Locations: United States, Oregon, Remote; United States, Washington, Remote Job ID R0000044755 Category Clinical Trials Date Posted 08/18/2026
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Success profile
Global Clinical Trial Experience Preferred
Extensive knowledge of clinical trial methodologies, ICH/GCP, Food and Drug Administration (FDA) and local country regulations
Must be fluent in English and in the native language(s) of the country they will work in
Travel within area is required
Valid driver’s license and passport required
Knowledge And Experience
Demonstrated knowledge of clinical research and development processes and ability to gain command of process details
Demonstrated knowledge of global and local regulatory requirements
Demonstrated understanding of key operational elements of clinical research (e.g., monitoring, data acquisition and cleaning, reporting, etc.)
Demonstrated knowledge in disease and technical areas pertaining to clinical studies, including knowledge of company direction, investigational product(s), and associated development plan(s)
Demonstrated ability to support sponsor regulatory interactions/inspections
Demonstrated knowledge of the processes around protocol design and feasibility assessment
Demonstrated understanding of region/country, culture, and medical practice and how they affect clinical trial delivery
Proven ability to work in a matrix team environment with the ability to influence, drive / lead and work through others for successful delivery of clinical trial
Ability to evaluate, interpret and present complex issues and data to support risk management and mitigation
Effective verbal and written communication skills in relating to colleagues and associates both inside and outside of the organization
Education
Bachelor’s degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical is required
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the United States includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
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Potential Career Path
Parexel offers various career paths and internal development programs for CRAs to advance to the next level. This could include enhancing your technical position, moving into management, or shifting to other areas of the business.
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CRA I
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Senior CRA
Project Management
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Employee Insights
Nick on a day in the life of a CRA
Nick Burger | Senior Clinical Research Associate
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Liliana on CRA tasks and our recognition program
Liliana Belmares Flores | CRA Line Manager
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Marlayna on why Parexel is a great place for CRAs
Marlayna Fitts | CRA Line Manager
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TEAM IMPRESSIONS
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Why Clinical Research Associates work at Parexel
Patient-focused in everything we do
We push the boundaries of what is possible to create clinical trials that are inclusive, innovative, and patient-focused
Supportive and inclusive environment
We foster collaboration, teamwork, respect, and inclusivity, to work together to achieve common goals.
Career growth and development
We develop your skills through training, mentorship, and career advancement programs.
Flexible work arrangements
We focus on outputs and results, not where and when you work.
Diverse therapeutic areas and project exposure
We continuously learn from a broad exposure from early to late phase clinical trials and our cros-functional global teams.
Advanced Technology
We recognize the importance of first-time quality to bring treatments to patients faster.
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Learn About Our Culture
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Learn More
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Learn More
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At Parexel, we prioritize putting people first, allowing you to achieve your best work. Explore the Flexible Work Program, our "Bravo" Recognition Program, and how we build our well-being in our supportive culture.
Learn More
Apply and matching require a free OVN account. Browse listings anytime without signing in.