Onsite PharmD Clinical Scientist – Early Drug Development

Pharmaceutical Company; South San Francisco (CA); Sur place; USD 96 000 - 152 000; Plein temps

Résumé du poste

Pharmaceutical Company in South San Francisco is seeking a Clinical Scientist to contribute to early-stage clinical development strategies, including safety and efficacy assessments of biomarkers and CDPs. You will gain exposure to Phase I/II drug development, trial execution, medical data review, and cross-functional collaboration within a pharmaceutical research environment.

Responsibilities include protocol development, study start-up documents, data reviews, regulatory support, and

Qualifications

• Doctor of Pharmacy (PharmD) degree from an accredited School of Pharmacy.
• Must be legally authorized to work in the United States.
• Strong attention to detail and commitment to scientific integrity and ethical standards.
• Excellent written and verbal communication skills.
• Strong organizational and project management skills, with the ability to prioritize multiple assignments and meet deadlines.
• Strong interpersonal and collaboration skills, including the ability to influence stakeholders without direct authority.
• Ability to work effectively in complex, cross-functional team environments.
• Strong presentation skills, with the ability to summarize scientific information and communicate key considerations and decisions.
• Demonstrated teamwork skills and the ability to drive discussions toward actionable outcomes.
• Strong interest in learning early-stage clinical drug development, particularly Phase I and Phase II clinical trials.

Responsabilités

• Participate in Clinical Science Sub-Teams (CSTs) and other relevant cross-functional teams to support clinical development activities.
• Prepare and present materials related to clinical study protocols, study execution, and interpretation of clinical development plans.
• Support or lead the development of clinical study protocols, Informed Consent Forms (ICFs), and clinical science study start-up documents.
• Conduct medical data reviews and collaborate with Data Management teams on data collection, review, and analysis strategies.
• Review, assess, and track protocol deviations on a regular basis.
• Draft protocol clarifications and amendments, ensuring associated ICFs and study documents are updated as required.
• Serve as an initial point of contact for protocol-related questions and study inquiries from internal stakeholders and external clinical sites.
• Support the preparation of clinical sections of regulatory documents and responses to health authority or ethics committee inquiries, under appropriate guidance.
• Collaborate with Safety Science teams to identify and track potential safety events during clinical studies.
• Contribute to strategic initiatives related to assigned molecules, clinical development plans, therapeutic areas, and portfolio priorities.
• Work collaboratively with cross-functional teams to ensure clinical deliverables are completed accurately and on schedule.

Connaissances

Communication

Attention to detail

Project management

Cross-functional

Presentation skills

Teamwork

Stakeholder influence

Formation

PharmD degree

Description du poste

Pharmaceutical Company in South San Francisco is seeking a Clinical Scientist to contribute to early-stage clinical development strategies, including safety and efficacy assessments of biomarkers and CDPs. You will gain exposure to Phase I/II drug development, trial execution, medical data review, and cross-functional collaboration within a pharmaceutical research environment.

Responsibilities include protocol development, study start-up documents, data reviews, regulatory support, and