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Associate Director Clinical Scientist Jobs (NOW HIRING)

Myana

Associate Director, Clinical Scientist

Waltham, MA · On-site

$161K - $202K/yr

Position Summary The Associate Director, Clinical Scientist is a highly collaborative, execution-focused role that supports the development, evaluation, planning and conduct of clinical studies. This ...

Kura Oncology

Assoc Dir/Director Clinical Scientist

$226K - $264K/yr

Serve as clinical science representative on cross-function teams as assigned. JOB SPECIFICATIONS ... The base range for an Associate Director is $180,000 - $222,000 and a Director is $226,000 - $264 ...

Verastem Oncology

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 ...

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

As of Sep 9, 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

Waltham, MA • On-site

Myana
See more jobs at Myanaexternal

$161K - $202K/yr

Other

Posted 22 days ago

Key responsibilities

  • Support the development, evaluation, planning, and conduct of clinical studies within the Neurology Therapeutic Area.

  • Contribute to the development and review of clinical and scientific content for study documents such as protocols, amendments, ICFs, IBs, and CSRs.

  • Perform ongoing review and interpretation of clinical trial data to ensure quality, safety, and protocol compliance.

Job description

Position Summary

The Associate Director, Clinical Scientist is a highly collaborative, execution-focused role that supports the development, evaluation, planning and conduct of clinical studies. This position ensures the scientific integrity and accurate interpretation of study data for clinical programs within the Neurology Therapeutic Area. Reporting to the Director, Clinical Scientist, the individual serves as a key scientific and clinical partner across global clinical programs, contributing directly to the authoring of clinical study documents, supporting trial conduct, and participating in cross‑functional study teams. The role works closely with Medical Directors to support medical monitoring activities, while partnering cross‑functionally with Clinical Operations, Data Management, Biostatistics, Translational Sciences, Medical Affairs, and Regulatory Affairs to translate clinical strategy into operational deliverables and ensure rigorous ongoing review of trial data for quality, safety, and protocol compliance.

Key Responsibilities
  • Actively contribute to the scientific development and execution of global clinical studies within the Neurology Therapeutic Area in alignment with the clinical development plan.
  • Contribute to the development and/or review of clinical and scientific content for core study documents, including clinical protocols, protocol amendments, informed consent forms (ICFs), investigator brochures (IBs), and clinical study reports (CSRs).
  • Perform ongoing, rigorous review and interpretation of emerging clinical trial data (both subject‑level and aggregate safety and efficacy data) to ensure quality, completeness, consistency, and protocol compliance.
  • Participate actively as a member of cross‑functional study teams to ensure the timely and high‑quality execution of clinical trial milestones.
  • Support the Director, Clinical Scientist in study execution activities, serving as a key clinical science resource and subject‑matter expert for the study team.
  • Contribute to the preparation, authoring, and revision of regulatory submissions and health authority responses, ensuring compliance with global guidelines.
Qualifications
  • Advanced scientific or clinical degree (e.g., PhD, PharmD, or equivalent clinical/scientific training).
  • Minimum of 3 to 5 years of relevant clinical research experience within the biopharmaceutical or biotechnology industry, with prior experience supporting neurology clinical trials preferred but not required.
  • Demonstrated experience in clinical trial conduct, including hands‑on data review, safety monitoring, and data cleaning processes.
  • Strong understanding of clinical development processes, regulatory requirements, and global guidelines (FDA, EMA/EU, ICH, and GCP) and applicable standard operating procedures.
  • Excellent communication and technical writing skills, with demonstrated experience drafting, reviewing, and editing scientific or clinical content for study‑related documents and clinical protocols.
  • Proven ability to work effectively and collaboratively in a fast‑paced, cross‑functional, team‑oriented professional environment.
  • Strong organizational skills with the ability to manage multiple priorities and drive sound results.
  • Willingness to travel 10-15% of the time, including travel to key medical conferences and study‑related events such as investigator meetings.
Compensation & Benefits

The base salary pay range for this role is $161,700 to $202,200. Actual compensation packages will depend on factors including depth of experience, education, skill set, overall performance and location. Additional compensation may include annual performance bonus, equity, full range of benefits and other incentive plans, providing a competitive total rewards strategy.

Equal Opportunity

Zenas BioPharma is proud to be an equal‑opportunity employer. We are committed to fostering an environment where diversity is valued. All qualified applicants will receive consideration for employment based on merit, qualifications and the needs of the business.

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