Clinical Study Manager / Senior Clinical Study Manager in San Diego, CA

$150K - $200K(Ladders Estimates)

Ambrx   •  

San Diego, CA 92101

Industry: Pharmaceuticals & Biotech

  •  

11 - 15 years

Posted 52 days ago

Major Responsibilities:

• Oversee all operational aspects of assigned clinical trials, drive excellence in clinical operations to ensure compliance with regulatory and GCP requirements to attain high quality and efficient clinical conduct, and achieve established goals within timelines and budget

• Work with internal stakeholders (clinical, legal, QA, finance) in line with company SOPs to select most suitable clinical CROs and vendors for clinical programs at different development stages, ensure assumptions, scope, vendor responsibilities, and payment terms are clearly defined through final contract approval

• Apply expertise in day to day clinical operations activities, collaborate with internal and external cross functional team members to develop study documents and manuals, including, protocol, ICF, CRFs, study monitoring plans, pharmacy manuals, site initiation presentation deck, site management plans, data management plan, and protocol deviation management plan, etc

• Coordinate site selection and Principal Investigator identification activities, including identification of KOLs

• Closely monitor and track study activities, ensuring timely data entry, query resolution, and prompt resolution of sites issues. Review CRA monitoring reports, proactively identifying and addressing study conduct issues

Job Qualifications

: • BS or MS in a biological science related field or equivalent experience with 10+ years of relevant experience in the clinical trial management • Working knowledge of US FDA GCP requirements, and ICH guideline. Prior experience in conducting MRCT is a plus

• Strong interpersonal skills with an ability to confidently interact with key internal and external stake holders including department heads, senior management, physicians, administrators, and consultants

• Successful track record in managing phase 1-3 clinical studies

• Proven organizational and collaborative skills essential

• Willing to travel up to 15% for SIV, co-monitoring, and coordinating investigator meetings • Excellent English written and verbal communication skills • Must be self-motivated, detail-oriented, and able to work effectively in a fast-paced environment with minimal supervision

Valid Through: 2019-9-25