Job Title: Clinical Trial Management Associate
Location: Foster City CA
Duration: 06 Months
Description:
FUNCTION: Clinical Operations – Biomarker and Bioanalytical Operations
EXAMPLE RESPONSIBILITIES:
• 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
REQUIREMENTS:
We are all different, yet we all use our unique contributions to serve patients. Please see the following for the qualifications and skills we seek for this role.
Minimum Education & Experience
• MA /MS /PharmD /PhD with some relevant clinical or related experience in life sciences.
• BA / BS / RN with 1 or more years’ 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
Knowledge & Other Requirements
• Demonstrated ability to be a fast learner.
• Demonstrated ability to be flexible and adaptable to change, to move between projects easily and provide support/expertise where needed.
• Aptitude to learn Gilead’s business and the biopharma industry.
• Teamwork and collaboration
• 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.
• Ability to communicate in a clear and concise manner.
• Ability to support a team-oriented, highly matrixed environment.
• Ability to execute multiple tasks as assigned.
• When needed, ability to travel.
