Senior Manager, Biosample Contractor

W2 Contract

Pay Rate: $55 - $65 per hour

Location: South San Francisco, CA - Onsite Role

Job Summary:

The Biosample Senior Manager will manage the biospecimen lifecycle for clinical programs through collaboration with Clinical Operations, Data Management, Clinical Outsourcing, Translational Medicine, Pharmacology scientists, and external vendors that support clinical studies.

Duties and Responsibilities:

• Development of biospecimen lifecycle strategies through close collaboration with project teams and scientists (for PK, ADA, PD/Biomarkers, and Safety)
• Ensure program-level consistency and cross-program standardization of biospecimen collection, processing, storage, and analysis.
• Contribute to the development of study protocols, ICFs, and other relevant study documents.
• Manage the creation of complex sample management plans and laboratory documents that ensure the proper collection and storage of samples at clinical sites and external vendors.
• Collaborate with Clinical Operations, Outsourcing, and Quality Assurance in the selection and oversight of central laboratories and specialty bioanalysis labs to ensure they meet study requirements and adhere to relevant compliance standards.
• Create systems and tools to manage sample analysis plans and enable study leads to deliver samples to appropriate analysis vendors on time.
• Facilitate external analysis vendor interactions with Data Management to ensure consistency in the transmission of sample metadata for accurate identification of analyzed samples.
• Lead process improvement projects and participate in cross-functional projects and working groups 

Requirements and Qualifications:

• A bachelor's degree in Biochemistry, Chemistry, Biology, Immunology, Neuroscience, Medical Technology, or a related field is recommended, plus at least 7 years of experience.
• Ability to lead effectively in a cross-functional team matrix environment
• Working knowledge of biosample management for clinical trials. Familiarity with relevant FDA & ICH/GCP regulations
• Ability to review and interpret clinical research protocols
• Technical know-how to create tools to solve operational challenges and improve workflows
• Previous experience in people management
• Entrepreneurial spirit with "can-do" attitude and commitment to work as part of a team
• Seeks change & values innovation
• Advanced planning and organization skills, and excellent analytical skills

Bayside Solutions, Inc. is not able to sponsor any candidates at this time. Additionally, candidates for this position must qualify as Inc.'s candidate.

Bayside Solutions, Inc. may collect your personal information during the position application process. Please reference Bayside Solutions, Inc.'s CCPA Privacy Policy at www.baysidesolutions.com.