To Discuss more about this job opportunity, please reach out to Deepak Arya (LinkedIn URL www.linkedin.com/in/deepakarya8a79aa22a/), email your updated resume at Email deepak.arya@collabera.com. Thank you!

Pay Range: $55 to $60 an hour.

Client Industry: Pharmaceutical
Job Mode: Remote
Duration: 06 Months (Possibilities of Extension)
Job Summary:

We are seeking an experienced Clinical Scientist to support early and late stage oncology clinical development programs. This position will provide scientific and clinical leadership across study design, protocol development, data review, and regulatory activities. The ideal candidate will collaborate with cross functional teams to execute clinical studies and drive strategic development initiatives. This role requires deep oncology expertise, strong clinical research knowledge, and the ability to communicate complex scientific information to diverse stakeholders. The successful candidate will play a critical role in advancing clinical programs while ensuring compliance with industry regulations and best practices.

Key Responsibilities:

• Partner with cross functional study teams to support execution of oncology clinical studies.

• Collaborate with Medical Directors to develop innovative clinical development strategies and study designs.

• Develop and maintain clinical trial protocols, study manuals, and clinical reports.

• Review informed consent documents, laboratory manuals, case report forms, clinical queries, and protocol deviations.

• Support investigator meetings, site initiation activities, and safety review committees.

• Perform routine review of clinical databases and study data.

• Identify clinical trends, safety findings, and efficacy signals within datasets.

• Review and validate clinical study reports and clinical sections of regulatory documents.

• Support regulatory submissions and responses to health authorities.

• Prepare scientific abstracts, posters, presentations, and internal clinical documents.

• Provide clinical development updates and scientific insights to leadership and stakeholders.

Required Qualifications:

• Advanced Clinical or Scientific Degree such as MD, PharmD, PhD, or MSN.

• Minimum 5 years of experience in Clinical Science, Clinical Research, Clinical Development, or related Oncology functions.

• Strong expertise in oncology clinical development.

• Experience reviewing and interpreting clinical safety and efficacy data.

• Knowledge of ICH guidelines, and regulatory requirements.

• Experience with protocol development and clinical trial execution.

• Strong written and verbal scientific communication skills.

• Excellent organizational and project management abilities.

• Ability to work independently with a high level of professionalism.

Preferred Qualifications:

• Experience supporting health authority interactions.

• Experience with Investigator Brochures and Development Safety Update Reports.

• Experience in biomarker driven clinical development.

• Knowledge of precision medicine approaches.

• Experience presenting at scientific and clinical conferences.

• Exposure to global clinical development programs.

Benefits: The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, long-term disability insurance, short-term disability insurance, paid parking/public transportation, (paid time , paid sick and safe time , hours of paid vacation time, weeks of paid parental leave, paid holidays annually - AS Applicable)