Senior Clinical Scientist
About The Position
The Senior Clinical Scientist is a key member of a clinical development team, supporting protocol development and study delivery. Working closely with the CDT Lead and other Clinical Representatives, the role performs delegated tasks in support of the clinical development program according to therapeutic-area and project needs. Under general direction, the position contributes scientific input to the development and execution of clinical studies, supports medical monitoring and study oversight, and collaborates with internal and external stakeholders to translate clinical strategy and protocols into operational deliverables. The role is hybrid, based onsite at one of the posted locations at least three days per week. Relocation assistance and visa sponsorship are not provided.
Requirements
- Bachelor’s degree or equivalent in a Life Sciences discipline.
- PhD with 3 or more years, MS with 4 or more years, or BS with 5 or more years of clinical research or clinical development experience in the biotechnology or pharmaceutical industry.
- Strong scientific framework and ability to work toward tangible outcomes, meet timelines, and ensure study delivery.
- Excellent written and oral communication skills.
- Ability to think beyond and maintain an external and strategic focus.
- Ability to build bridges and help teams develop collaboration.
- Ability to unleash outcomes and create an accountable work environment.
- Ability to ignite agility and instill personal flexibility in oneself and teams.
- Ability to inspire the future and ensure clarity around strategy.
Nice To Haves
- An advanced degree (MS or PhD) in a Life Sciences discipline.
Responsibilities
- Contribute to the scientific development of individual clinical studies in alignment with the approved clinical development plan.
- Provide scientific input to support safe, efficient, timely, high-quality, and compliant execution of assigned programs.
- Contribute to program and core clinical development documents and training materials aligned with the scientific strategy, including clinical development plans, investigator brochures, protocols, eCRFs, informed consent forms, study reference manuals, and investigator training.
- Review clinical data with some assistance and assist with interpreting clinical study data.
- Write, edit, or review study results in study reports, regulatory submissions, abstracts, posters, presentations, peer-reviewed manuscripts, and other documents.
- Support medical monitoring and oversight of individual clinical studies to promote patient safety and data integrity.
- Manage processes and interactions supporting external study oversight committees, such as steering committees, independent data monitoring committees, and adjudication committees.
- Collaborate with internal and external cross-functional stakeholders to translate clinical development strategy and clinical protocols into operational deliverables.
- Contribute to multidisciplinary working groups supporting continuous process improvement, as requested.
Benefits
- Incentive compensation may be included in total compensation.
- Equity may be included in total compensation.
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What This Job Offers
Job Type
Full-time
Career Level
Senior
