Director, Clinical Research Scientist - Perm - New York
Proclinical is seeking a Director, Clinical Research Scientist to join the Clinical Development team at an established biotech. In this role, you will be instrumental in the strategic planning, design, and execution of clinical-stage programs.
Primary Responsibilities:
The successful candidate will work closely with the Clinical Operations Team to support and execute clinical trials and may serve as the lead Clinical Research Scientist on specific studies or programs.
Skills & Requirements:
- Advanced degree in Life Sciences (MD, PhD, Pharm D, MS, RN, or similar).
- Experience in the pharma/biotech industry or relevant clinical/laboratory research.
- Experience with clinical trials and knowledge of Good Clinical Practice.
- Strong interpersonal, verbal, and written communication skills.
- Analytical and presentation skills.
- Ability to work independently and in a team setting.
- Comfortable in a fast-paced, entrepreneurial environment.
- Ability to travel up to 20%.
- In-office presence required 4 days per week.
The Director, Clinical Research Scientist's responsibilities will be:
- Support the clinical development of assigned programs and participate in the design and implementation of development strategies.
- Collaborate with clinical operations and cross-functional teams to execute clinical trial activities.
- Co-lead study team meetings with Clinical Operations study leads.
- Provide clinical/medical monitoring and associated documentation.
- Act as the primary point-of-contact for clinical science-related activities.
- Conduct ongoing medical/safety data reviews in collaboration with Clinical Sciences Physicians.
- Engage with internal and external partners, including key opinion leaders, clinical investigators, and health authorities.
- Develop and present Protocol and ICF documents/amendments.
- Independently resolve critical problems and ensure data collection aligns with protocols.
- Prepare clinical presentation slides and materials for various meetings and communications.
- Contribute to internal documents, regulatory submissions, and external publications.
- Participate in the development and enhancement of clinical development processes and tools.
- Engage in competitive intelligence and market assessment activities.
- Maintain scientific and clinical knowledge in oncology and related therapeutic areas.
Compensation:
- USD 150 000.00 - 175 000.00 per annum
If you are having difficulty in applying or if you have any questions, please contact Nico Kohlwes at n.kohlwes@proclinical.com
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
