Oncology Field Medical, Director (MD), Solid Tumors and Early Pipeline The Oncology Field Medical, Director is responsible for providing therapeutic area/product expertise for Solid Tumors (primarily CRC and Melanoma) as well as Early Pipeline support across a broad range of Medical customer segments and initiatives...

Your Future Evolves Here Evolent partners with health plans and providers to achieve better outcomes for people with most complex and costly health conditions. Working across specialties and primary care, we seek to connect the pieces of fragmented health care system and ensure people get the same level of care and ...

St. Peters Health Partners is seeking a dedicated Physician specializing in Medical Oncology and Hematology to join their team in Albany and Troy, NY. This role involves providing patient-centered care within a collaborative environment, supported by dedicated APPs, nurses, and pharmacists. The position offers a sta...

The Oncology Translational Medicine (OTM) Planning & Execution team is a dedicated group of Scientific Operations, Project Management, and Alliance Management professionals that integrate, manage, and drive execution of OTM's biomarker and diagnostic strategies across GSK's global Oncology portfolio. The Director, A...

The Department of Medicine of the University Of Maryland School Of Medicine and the Marlene and Stewart Greenebaum Comprehensive Cancer Center (UMGCCC), located in Baltimore, MD are recruiting for a full-time Medical Director of the University of Maryland St. Joseph Cancer Institute, located in Towson, MD. General ...

6AM City, LLC is seeking a Medical Director - Oncologist for a Large Managed Care Organization in NJ. The role involves reviewing and denying cases to enhance clinical outcomes and patient experience while also improving efficiency and reducing costs. The ideal candidate will have a strong background in Internal Me...

"Bridging Innovation to Cure "Developing and manufacturing your cell therapies from benchtop to bedside" Job Summary Cellipont Bioservices is growing, and we are looking for a Manufacturing Associate I who believe in the potential bridging client's discoveries to patient cures and who want to challenge the status...

Description About Celularity Celularity Inc. (Nasdaq: CELU) is a longevity-focused regenerative and cellular medicine company developing and manufacturing allogeneic and autologous cell therapies derived from the postpartum placenta. Celularity leverages the placenta’s unique biology, immunologic properties and sc...

An established industry player is seeking a Senior Project Manager to lead complex projects in cell therapy development and operations. This role demands a proactive leader with a proven track record in GxP project management and a deep understanding of regulatory requirements. You will manage critical projects, ens...

About Krystal Bio: At Krystal Biotech, we bring together the brightest and most eager minds to relentlessly pursue the discovery, development, manufacturing, and commercialization of genetic medicines to treat diseases with high unmet medical needs. Founded in 2016, Krystal is distinguished in three powerful ways:...

We've made a lot of progress since opening the doors in 1942, but one thing has never changed - our commitment to serve, heal, lead, educate, and innovate. We believe that every award earned, every record broken and every patient helped is because of the dedicated employees who fill our hallways. At Ochsner, whethe...

Job Requirements Night Shift - 8pm-8:30am Job Summary Under the direct supervision and delegation of a Registered Nurse, participates in the nursing process by providing supportive patient care to patients and their families. Assists with delegated direct care activities as required for daily operations on the as...

Team Net Medical seeks a motivated Medical Physicist Trainee in Fredericksburg, Virginia to join its radiation oncology team. The role offers supervised clinical experience in medical physics and responsibilities such as quality assurance, treatment planning support, and ensuring compliance with radiation safety. I...

A clinical-stage biotech company is seeking a Director of Drug Safety & Pharmacovigilance in Boston, MA. This role includes developing and implementing pharmacovigilance strategies for clinical programs in oncology and inflammatory diseases, providing expert safety guidance, and managing safety operations. Candidate...

SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs...

ICON is seeking an Experienced Senior Manager of Pharmacovigilance to manage global pharmacovigilance activities tied to oncology products. This hands-on role is crucial in ensuring compliance with safety regulations and collaborating with cross-functional teams. Ideal candidates will possess over 12 years of exper...

As an Associate Director you will lead the development and execution of global CMC regulatory strategies for the hematology and oncology portfolios. You will guide regulatory activities across development stages, mentor CMC Regulatory Affairs (RA) staff, supporting cross-functional and external partners, and serving...

A leading biotechnology company in Troy, NY, seeks an Associate Director to develop global CMC regulatory strategies for hematology and oncology portfolios. Responsibilities include leading regulatory activities, mentoring staff, and guiding interactions with regulatory authorities. The ideal candidate has over 10 ...

Salary: $154,000-$215,000 Location: Remote (US) Core hours: Eastern or Central Time Why Work With Us At Candel, our people drive our success. We value diversity, collaboration, and bold thinking in a supportive, mission-driven environment. We are a high-performing team that shows up for each other and stays focused ...

Florida Cancer Specialists & Research Institute is seeking an individual responsible for maintaining regulatory compliance and managing clinical documentation in Bunnell, Florida. The role involves creating regulatory files, ensuring timely submissions to IRB, and conducting monitoring activities. Applicants should...

Bio Space is seeking a Director of Regulatory Affairs to lead global regulatory activities for clinical product filings. You will be responsible for IND/CTA and BLA submissions, requiring strong leadership and critical thinking skills. The ideal candidate will have a medical degree and at least 10 years in the phar...

Duke Clinical Research Institute in Durham, North Carolina is seeking a Regulatory Coordinator to manage regulatory operations for complex oncology studies. Responsibilities include preparing documentation, ensuring compliance, supporting audits, and coordinating study activities. The ideal candidate should have an...

The Senior Manager of Regulatory Affairs, Oncology will assist in all facets of the company’s Regulatory Affairs for all U.S. and international regulatory matters, including filings and interactions with regulatory authorities. This is a REMOTE role based in the US. Principal Duties and Responsibilities include th...

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell ...

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell ...

AstraZeneca GmbH is seeking a Statistical Programming Director to lead programming efforts within Oncology Biometrics. This role involves managing a team and ensuring high-quality deliverables for phase 1/2 trials across various cancer indications. The ideal candidate will have extensive experience in clinical drug...

Position: Oncology Biostatistician: Real-World & Genomic Analyses Apr is looking for a Biostatistician to join their oncology research team, supporting data quality and analysis in a collaborative environment. The ideal candidate will have advanced statistical expertise and the ability to contribute to impactful re...

Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the U.S. (Sumitomo Pharma America, Inc.), focused on addressing patient needs in oncology, urology, women's health, rare diseases, cell & gene therapies and CNS. With several marketed products and a diverse pipeline of ea...

Job Summary The SrCRA role is responsible for supporting monitoring and site management activities for the client Sponsored studies. Site monitoring and site management activities are conducted according to ICH GCP, applicable country/local regulations and client SOPs. Site interactions are conducted both on-site an...

Must be located in Florida. JOB SUMMARY The SrCRA role is responsible for supporting monitoring and site management activities for the client Sponsored studies. Site monitoring and site management activities are conducted according to ICH GCP, applicable country/local regulations and client SOPs. Site interactions...

A leading clinical research organization in Connecticut is seeking a Clinical Research Associate with over two years of on-site monitoring experience, particularly in Oncology studies. The role involves ensuring compliance, conducting site visits, and collaborating with cross-functional teams. Candidates must hold a...

Senior Oncology CTMS Analyst (Contract) Location: Miami, FL Contract (15 Weeks) Schedule: Monday – Friday | 8:30 AM – 5:00 PM Pay: $28.00 – $38.00 per hour An established hospital in the Miami area is seeking an experienced Senior Oncology CTMS Analyst for a 15-week contract assignment. This role is ideal for a hea...

This Assistant Clinical Research Manager (ACRM) position will work within the Breast Oncology clinical research program and assist in the management of the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator. Thesepositions, in collabo...

Merck & Co. is seeking a Clinical Study Manager in Basking Ridge, New Jersey. The role entails leading the delivery and execution of global clinical studies, ensuring compliance and managing vendor relationships. Candidates must have a Bachelor's Degree in Life Sciences and at least 3 years of experience in clinical...

Who we are We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are World...

AbbVie is hiring for a role focused on overseeing the direction and execution of clinical trials in the United States, Illinois. The position requires managing clinical study protocols and ensuring adherence to regulatory standards. The ideal candidate holds a Bachelor's degree in the sciences, has clinical researc...

POSITION SUMMARY You will be responsible for scientific oversight, data integrity and quality of clinical trial(s) in support of the development strategy for programs within the Late-Stage Oncology portfolio. KEY RESPONSIBILITIES Clinical development expert for assigned studies maintaining current scientific and cli...

Clinical Scientist - Oncology Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the ...

Job Summary Oversees all clinical pharmacology activities related to pre‑IND, IND, phase 1‑3, PK, PK/PD and regulatory submissions. Leads study design, execution and reporting of clinical pharmacology and studies. Provides input into all phases of drug development including, but not limited to dose finding, dose opt...

Scientist – Biomarker Development (m/f/d) Full-time Be part of our team We are seeking an experienced and highly motivated (Senior) Scientist to join our Biomarker Development team. The ideal candidate holds a PhD in Life Sciences, Biology, or a related field, and has advanced expertise in immunohistochemistry (IH...