Senior Manager, Clinical Scientist - Contract - New Jersey, REMOTE
ذكذكتسئµ is seeking a Senior Manager, Clinical Scientist to support oncology-focused clinical development programs. This is a fully remote W-2 contract role with an initial duration of six months.
Primary Responsibilities:
The successful candidate will play a key role in the planning, execution, and evaluation of clinical studies, ensuring data integrity and contributing to the success of early- and late-phase development projects. You will collaborate closely with cross-functional teams and provide scientific expertise to drive clinical trial design and delivery.
Skills & Requirements:
- Bachelor's degree required; advanced degree (PhD, MD, PharmD, MSc) in life sciences or healthcare preferred.
- Proven experience in pharmaceutical clinical drug development, with knowledge of the drug development process, GCP, and clinical research methodology.
- Strong medical writing skills and familiarity with regulatory requirements and ICH-GCP guidelines.
- Demonstrated ability to influence within teams and across functions.
- Strong analytical, problem-solving, and interpersonal skills.
- Experience working cross-functionally and managing complex issues creatively and effectively.
- Considerable organizational awareness and a track record of clinical trial process improvements.
The Senior Manager, Clinical Scientist's responsibilities will be:
- Contribute to program team meetings, scientific advisory boards, study steering committees, and data-safety monitoring meetings.
- Serve as a member of the Clinical Study Team and Global Clinical Sub-Team.
- Develop and maintain a deep understanding of therapeutic disease areas, drug candidates, and their mechanisms of action.
- Support the initiation and execution of clinical research studies, including authoring or reviewing sections of clinical trial protocols, amendments, and other trial-related documents.
- Assist with the development of regulatory documents and perform quality reviews.
- Ensure compliance with FDA, EMEA, ICH, GCP guidelines, and applicable SOPs regarding clinical safety.
- Conduct clinical and medical data reviews, including safety monitoring and patient safety procedures.
- Identify critical risks and propose mitigation strategies to ensure study objectives are met.
- Promote consistent clinical data review techniques and conventions across assigned studies.
Compensation:
If you are having difficulty in applying or if you have any questions, please contact Bodin Forsen at b.forsen@proclinical.com
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
ذكذكتسئµ is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. ذكذكتسئµ is acting as an Employment Agency in relation to this vacancy.
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