Lead impactful hematology clinical studies in a dynamic contract role. Collaborate across functions to design and execute innovative clinical programs. Gain valuable experience in global clinical trial execution.
Associate Director Clinical Scientist
in Healthcare + Life Sciences ContractJob Detail
Job Description
Overview
- Contribute to the development and execution of hematology clinical studies, ensuring scientific integrity and data interpretation.
- Collaborate within a matrix environment, supporting cross-functional teams and candidate development projects.
- Provide scientific expertise for designing and delivering clinical studies and programs.
- Develop clinical trial protocols, amendments, and regulatory documents with minimal guidance.
- Prepare and present data for external stakeholder meetings and internal collaborators.
- Promote consistent medical/clinical data review techniques across studies and programs.
- Identify risks and design mitigation strategies to ensure successful program objectives.
- Maintain a proficient understanding of therapeutic disease areas and drug candidates.
Key Responsibilities & Duties
- Function as Clinical Scientist for programs, contributing to team meetings and collaborative activities.
- Utilize scientific expertise to propose, design, and execute clinical research studies.
- Author and review clinical trial protocols, informed consents, and study reports.
- Support the development of regulatory documents and ensure quality review.
- Prepare information for external stakeholder meetings and present data effectively.
- Promote consistent medical data review techniques across studies and programs.
- Identify risks in clinical programs and design effective mitigation strategies.
- Collaborate closely with Medical Directors to ensure program success.
Job Requirements
- Bachelor’s degree required; advanced degree in life sciences or healthcare preferred.
- Minimum of 10 years of pharmaceutical clinical drug development experience.
- Proficient knowledge of drug development processes, Good Clinical Practice, and clinical research methodology.
- Strong medical writing skills and ability to develop clinical trial documents.
- Experience in conducting global clinical trials and executing clinical programs.
- Solid understanding of oncology or hematology therapeutic areas preferred.
- Demonstrated ability to influence within teams and across functions.
- Strong cross-functional management and interpersonal skills.
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