Assoc Dir/Director Clinical Scientist

This role supports clinical priorities focused on quality, patient-centered outcomes, and effective care delivery. You will collaborate with clinical leaders, operational teams, and cross-functional stakeholders to improve standards, workflows, and execution within a life sciences environment.

Responsibilities

• Lead development of clinical study protocols based on strategic concepts
• Collaborate on trial design elements, including CRF and data review plans
• Analyze and interpret study results, ensuring accurate data reporting
• Identify issues through data monitoring and develop strategic solutions
• Support the creation of regulatory documents for product approvals
• Assist in target engagement assay implementations for dose selection
• Communicate study results effectively to internal and external stakeholders

Qualifications

• Advanced clinical or science degree (RN, MA, PharmD, NP, PhD)
• Minimum of 5 years' experience post-MA or 3 years post-PharmD/PhD
• Experience with planning, executing, and reporting clinical studies in pharma
• Ability to summarize and present study data effectively
• Fluent in written and verbal English
• Understanding of the drug development process, from pre-IND to post-registration
• Broad knowledge of drug development functions, including regulatory and clinical operations

Location: Remote - US based candidates only, no visa sponsorship available

Pay

$180,000 – $264,000 annually

Benefits

• Career advancement and development opportunities
• Competitive compensation package with bonus
• 401K plan with employer contributions
• Generous stock options and Employee Stock Purchase Plan (ESPP)
• 20 days of PTO plus 18 holidays including breaks
• Comprehensive benefits package with employer match
• Paid maternity/paternity leave
• Catered lunches in-office
• Lifestyle spending stipend and commuter stipend for Boston office
• Regular social activities to foster team bonding