Associate Director, Clinical Scientist

Associate Director, Clinical Scientist – Contract — Boston, REMOTE USA

Proclinical is seeking an Associate Director, Clinical Scientist to join a fast-paced Immunology Clinical Research team on a contract basis. This remote role is based in the USA, and applicants must be authorized to work without sponsorship.

• The successful candidate will play a key part in the design, execution, and scientific oversight of clinical studies, ensuring the integrity and interpretation of study data.
• You will work collaboratively in a matrix environment with cross-functional teams, contributing to both early and late-phase development programs.

• Bachelor's degree required; advanced degrees (PhD, MD, PharmD, MSc) in life sciences or healthcare preferred.
• Proven experience in pharmaceutical clinical drug development, with a strong track record in global clinical trials and program execution.
• Comprehensive knowledge of the clinical development process, regulatory requirements, and ICH-GCP guidelines.
• Strong cross-functional management, interpersonal, and problem-solving skills.
• Ability to lead within a matrix environment, demonstrating confidence, diplomacy, and influence.
• Analytical expertise to assess program objectives and design impacts on data analysis.
• Initiative, creativity, and innovation in resolving complex problems and improving processes.

• Serve as the lead Clinical Scientist for assigned programs or act as a delegate for the Therapeutic Area Lead Clinical Scientist.
• Participate in program team meetings, scientific advisory boards, study steering committees, and data-safety monitoring meetings.
• Represent the function in collaborative activities with other departments and external stakeholders.
• Maintain a strong understanding of therapeutic disease areas, drug candidates, and relevant regulatory guidelines (FDA, EMEA, ICH, GCP).
• Propose, design, and execute clinical research studies, contributing to strategy development supported by scientific literature.
• Develop and review clinical trial protocols, amendments, informed consents, medical monitoring plans, SAPs, and clinical study reports.
• Lead planning and preparation for external stakeholder meetings, including investigator meetings, governance reviews, and regulatory authority presentations.
• Conduct clinical and medical data reviews, including safety monitoring, to ensure patient safety.
• Identify risks and design mitigation strategies while promoting consistent clinical data review practices across studies.
• Provide mentorship and guidance to junior team members and cross-functional colleagues as needed.

• $95.00 - $120.00 Per Hour

If you are having difficulty applying or have any questions, please contact Bodin Forsen at .

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.

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