$130,000-$160,000/year
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Clinical Trial Manager
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San Francisco, CA (Hybrid)
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Job Description
A cutting-edge pharmaceutical oncology company is seeking a highly motivated and detail-oriented Clinical Trial Manager to help revolutionize cancer treatment. In this role, you will play a crucial part in the planning, execution, and management of clinical trials, ensuring the successful development of life-changing medical products. As a Clinical Trial Manager, you'll have the chance to work on pioneering clinical trials that are at the forefront of scientific advancements. Their groundbreaking research harnesses AI-driven drug discovery, precision medicine, and immunotherapies to target cancer cells with unprecedented accuracy. You'll be an essential part of the mission, leading and guiding cross-functional teams towards the successful execution of groundbreaking clinical trials.
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Responsibilities:
Lead the planning, initiation, and execution of clinical trials in accordance with approved protocols, GCP guidelines, and regulatory requirements.
Collaborate with key stakeholders, including Clinical Operations, Data Management, Regulatory Affairs, and Investigator Sites, to ensure seamless coordination and effective trial implementation.
Develop and manage trial budgets, resource allocation, and timelines to achieve study objectives within specified timelines.
Oversee the selection and qualification of investigative sites, as well as training of site personnel on study protocols and procedures.
Conduct regular site monitoring visits and provide guidance to ensure adherence to study protocols, data integrity, and participant safety.
Facilitate communication and maintain a strong relationship with study investigators, sponsors, and CRO partners.
Ensure timely and accurate reporting of trial progress to internal and external stakeholders
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Qualifications:
Bachelor's degree in life sciences, pharmacy, or a related field; advanced degree is a plus.
Proven experience (minimum 5 years) as a Clinical Trial Manager within the pharmaceutical or biotechnology industry.
Comprehensive understanding of clinical trial regulations, GCP guidelines, and industry best practices.
Strong project management skills with a track record of successfully managing complex clinical trials.
Excellent leadership, communication, and negotiation skills with the ability to build and maintain effective working relationships.
Proficient in problem-solving and decision-making, capable of resolving challenges and making data-driven decisions.
Experience working with CROs and managing outsourced clinical trial activities.
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Benefits:
Medical Insurance
PTO
401(k)
