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Clinical Trial Associate
3 weeks ago
Responsibilities:
- Excellent employment opportunity for a Clinical Project Assistant II in the Foster City, CA area.
- FUNCTION: Clinical Operations – Biomarker and Bioanalytical Operations
- Responsible for the worldwide execution of all Phase I - IV clinical trials across all company therapeutic areas.
- Clinical Operations plays a key role in ensuring all company clinical trials are performed in accordance with applicable SOPs, company policies and regulatory guidelines to provide timely and high-quality clinical data that supports global registration and commercialization of company’s products.
- Support other Biomarker and Bioanalytical Operations team members in the start-up, maintenance and close-out of clinical studies.
- Track and prepare study-specific information, review and participate in the quality assurance of data and/or documents, arrange and assist with meetings and meeting logistics, and assist with development of documents and standard forms.
- Tracks and prepares study-specific information using databases, spreadsheets, and other tools.
- Reviews and participates in the quality assurance of data or documents.
- Arranges meeting logistics, agendas, and assists with minutes.
- Interacts with other departments, as needed, to complete assigned tasks.
- Assists with development of documents and standard forms.
- Ensures own work complies with established practices, policies and processes, and any regulatory or other requirements.
- Work with cross-functional team members across the Oncology, Inflammation and Virology therapeutic areas
- May support sample reconciliation for active clinical studies in collaboration with BBOps Study leads on sample tracking with periodic consent verification.
- Support sample reconciliation for active clinical studies in collaboration with BBOps Study leads on sample tracking with periodic consent verification.
- Experience with eTMF/Veeva system and support eTMF filing
- Participate in oral presentations as applicable
Experience:
- MA /MS /PharmD /PhD with some relevant clinical or related experience in life sciences.
- BA / BS / RN with 1 or more years of relevant work experience.
- Some general clinical or business knowledge and experience is preferred.
- Working knowledge and experience with Word, PowerPoint and Excel
- Excellent verbal, written, interpersonal and presentation skills are required
- Demonstrated ability to be a fast learner.
- Aptitude to learn company’s business and the biopharmaceutical industry.
- Good analytical and organizational skills
- Knowledge of Food & Drug Administration (FDA), European Medicines Agency (EMA), and other applicable national regulations, International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH) guidelines and Good Clinical Practice (GCP) is preferred.
- Understands how to use basic office programs / tools.
- When needed, ability to travel.
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