Senior Clinical Scientist
DataStaff, Inc. is seeking a Senior Clinical Scientist for a long-term contract opportunity with one of our direct clients in Raleigh, NC.
Possible contract to hire.
Job Description:
The Senior Clinical Scientist plays a critical part within a global research and development organization focused on advancing clinical programs in the aesthetics/medical field. The Senior Clinical Scientist provides scientific leadership and strategic input across the lifecycle of clinical development activities, from early planning through execution and reporting. Working closely with multidisciplinary teams, this individual contributes to study design, data evaluation, and interpretation to support regulatory approval and lifecycle management of products and indications. The position requires a proactive, detail-oriented professional capable of translating complex scientific data into clear, actionable insights.
Key Responsibilities:
Contribute scientific expertise to the design and planning of clinical studies across development phases. Collaborate with internal and external stakeholders, including cross-functional teams and subject matter experts. Support programs involving medical devices, pharmaceuticals, biologics, and related healthcare products. Integrate data from diverse sources to inform development strategies. Assist in early-stage development activities and identify risks, challenges, and solutions. Ensure clear communication of study progress.
Author, review, and finalize key clinical documents such as study protocols and reports. Interpret and communicate clinical data and ensure documentation meets regulatory standards and Good Clinical Practice. Support preparation of materials for stakeholder meetings.
Provide scientific input during study execution, contribute to outcome assessments, and support analysis and reporting of results. Contribute to regulatory documents and ensure proper disclosure of clinical trial data.
Prepare and present clinical findings and contribute to publications. Oversee external medical writing vendors to ensure quality and compliance.
Qualifications:
Master’s degree in Life Sciences required; advanced degree (PhD, DrPH, or MD) preferred. Strong understanding of clinical development, regulatory requirements, and technical writing required. Ability to manage multiple projects and adapt to changing priorities.
Additional Information:
Contract role with potential for permanent placement. Travel up to 5% may be required. Relocation may be required for long-term employment.
This opportunity is available on a corp to corp basis or as a W2 position with a competitive benefits package. DataStaff, Inc. offers medical, dental, and vision coverage options as well as paid vacation, sick, and holiday leave. As many of our opportunities are long-term, we also have a 401k program available for employees after 6 months.