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Associate Director Clinical Scientist Jobs (NOW HIRING)

Verastem

Director, Clinical Scientist

Needham, MA · On-site

$200K - $260K/yr

The Director, Clinical Scientist provides clinical and scientific leadership for assigned oncology studies and programs. This individual serves as a key member of Study and Program Teams, leading ...

Verastem

Director, Clinical Scientist

Needham, MA · On-site

$200K - $260K/yr

The Director, Clinical Scientist provides clinical and scientific leadership for assigned oncology studies and programs. This individual serves as a key member of Study and Program Teams, leading ...

Dyne Tx

Director, Clinical Scientist Department: 1240GL - Clinical Development Location: Waltham, MA Company Overview: Dyne Therapeutics is focused on delivering functional improvement for people living with ...

Dyne Tx

Director, Clinical Scientist

Waltham, MA · On-site

Director, Clinical Scientist Department: 1240GL - Clinical Development Location: Waltham, MA Company Overview: Dyne Therapeutics is focused on delivering functional improvement for people living with ...

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Associate Director Clinical Scientist information

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How much do associate director clinical scientist jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for associate director clinical scientist in the United States is $54.75, according to ZipRecruiter salary data. Most workers in this role earn between $40.14 and $68.27 per hour, depending on experience, location, and employer.

What does an associate director clinical scientist do?

An Associate Director Clinical Scientist is responsible for leading and managing clinical research activities within a pharmaceutical or biotechnology company. They oversee the design, implementation, and analysis of clinical trials, ensuring scientific integrity and regulatory compliance. This role also involves collaborating with cross-functional teams, interpreting clinical data, and contributing to the development of clinical strategies for drug development. Associate Directors often mentor junior staff and play a key role in communicating results to stakeholders.

What are the key skills and qualifications needed to thrive as an associate director clinical scientist?

To thrive as an Associate Director Clinical Scientist, you need an advanced degree in life sciences or medicine, extensive clinical research experience, and a deep understanding of drug development processes. Familiarity with clinical trial management systems, regulatory submission tools, and relevant certifications such as GCP are typically required. Strong leadership, strategic thinking, and excellent communication skills help drive cross-functional teams and effectively present scientific data. These competencies are crucial for ensuring robust clinical trial design, regulatory compliance, and impactful scientific contributions to pipeline advancement.

What are some common challenges faced by an associate director clinical scientist when managing cross-functional clinical project teams?

An Associate Director Clinical Scientist often encounters challenges in aligning diverse teams, such as clinical operations, data management, and regulatory affairs, toward common project goals. Balancing scientific rigor with operational timelines requires strong communication and negotiation skills, especially when addressing conflicting priorities or resource constraints. Additionally, ensuring compliance with evolving regulatory standards and maintaining data integrity across global studies can add complexity. Success in this role often depends on proactive problem-solving and fostering a collaborative team environment.

What is the difference between Associate Director Clinical Scientist vs Clinical Scientist?

AspectAssociate Director Clinical ScientistClinical Scientist
Required CredentialsTypically requires a PhD or MD, with several years of experience in clinical researchUsually requires a Bachelor's, Master's, or PhD in a related field
Work EnvironmentLeads cross-functional teams, involved in strategic planning and oversightConducts clinical trials, data analysis, and supports study operations
Employer & Industry UsageCommonly found in pharmaceutical and biotech companies, often in senior rolesFound across industry settings, including CROs and pharma, in operational roles

The Associate Director Clinical Scientist typically holds a more senior, strategic role with leadership responsibilities, while the Clinical Scientist focuses on executing clinical research activities. Both roles require strong scientific expertise, but the Associate Director often oversees projects and teams, guiding overall clinical development efforts.

What cities are hiring for Associate Director Clinical Scientist jobs?

Cities with the most Associate Director Clinical Scientist job openings:

What are popular job titles related to Associate Director Clinical Scientist jobs?

For Associate Director Clinical Scientist jobs, the most frequently searched job titles are:

Infographic showing various Associate Director Clinical Scientist job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 74% Full Time, 15% Part Time, and 8% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $113,877 per year, or $54.7 per hour.

Associate Director, Clinical Scientist, Ophthalmology

Tarrytown, NY • On-site

Scorpion Therapeutics
51 - 200 employees
Learn more about Scorpion Therapeuticsexternal

Other

Posted 12 days ago

Job description

Discover Your Role
  • May function as Clinical Scientist for program and/or delegate of Therapeutic area Clinical Scientist.
  • Contribute to program team meetings, scientific advisory boards, study steering committees, and data/safety monitoring meetings; represent function in cross-department activities.
  • Maintain understanding of therapeutic disease biology, clinical manifestations, standard practice, and drug candidate/landscape (mechanism of action).
  • Propose, design, and execute early and/or late-stage clinical research and development studies; communicate evidence-based strategy proposals.
  • Develop Expanded Synopsis; author/review protocol and amendment scientific content; author/review medical monitoring plans, SAPs, informed consents, and Clinical Study Report clinical components; support regulatory documents; perform quality review/approval and resolve cross-functional comments.
  • Plan and prepare materials for stakeholder meetings; present data to external investigators (SIV) and internal collaborators.
  • Use analytical skills to understand how objectives/design impact data analysis; identify risks and mitigation strategies.
  • Promote consistent first-line medical/clinical data review practices; review clinical data review plan and medical monitoring plan.
This Role Requires
  • Advanced degree or equivalent in life science/healthcare preferred (PhD/PharmD/MSc).
  • ≥10 years pharmaceutical clinical drug development experience, including basic Ophthalmology knowledge.
  • Proficient in drug development process, Good Clinical Practice, study design, clinical research methodology; solid medical writing skills.
  • Experience conducting global clinical trials and executing clinical programs.
  • Strong team-player; confidence and diplomacy; ability to influence within and across functions.
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