PharmD Clinical Scientist: Protocol & Development

Sharp Decisions; South San Francisco (CA); On-site; USD 140,000 - 190,000; Full time

Job summary

Sharp Decisions is seeking an experienced PharmD professional for a Clinical Development role in South San Francisco, CA. You will participate in Clinical Science sub-teams and contribute to protocol development, CDP execution, and regulatory document preparation.

This role requires strong communication, data review, and project-management skills to support multiple studies. You will collaborate across functional teams, ensure ethical and scientific rigor, and help drive safety assessments and

Qualifications

• PharmD degree from an accredited school.
• Eligible to work in the United States.
• Pharmaceutical/biotech internship or industry experience preferred.
• Experience in complex, matrixed environments.
• Strong ethics and scientific integrity.
• Excellent attention to detail and organizational skills.
• Strong written and verbal communication and presentation skills.
• Ability to manage multiple tasks and meet deadlines.

Responsibilities

• Participate as a standing member of the Clinical Science Sub-Team and/or ad hoc member of relevant sub-teams.
• Prepare or present materials related to development, execution, or interpretation of protocols and CDP aspects.
• Support or lead development of study protocols, ICFs, and startup documents.
• Conduct medical data reviews and collaborate with data management on data collection and analysis strategies.
• Review protocol deviations and draft clarifications or amendments as needed.
• Act as initial contact for protocol-related inquiries from internal teams and external sites.
• Assist in regulatory document preparation and HA/ethics inquiries with Clinical Science and team members.
• Collaborate with Safety Science to identify potential safety events within a study.
• Support strategic initiatives related to molecules, CDP, therapeutic areas, or portfolio.

Skills

PharmD

US work eligibility

Clinical development

Protocol development

Regulatory writing

Data review

Cross-functional collaboration

Attention to detail

Project management

Communication

Education

Doctor of Pharmacy (PharmD)

Tools

GxP systems

Job description

Sharp Decisions is seeking an experienced PharmD professional for a Clinical Development role in South San Francisco, CA. You will participate in Clinical Science sub-teams and contribute to protocol development, CDP execution, and regulatory document preparation.

This role requires strong communication, data review, and project-management skills to support multiple studies. You will collaborate across functional teams, ensure ethical and scientific rigor, and help drive safety assessments and