Senior Clinical Project Manager

Senior Clinical Project Manager

San Diego, CA - Hybrid

$120,000 - $160,000

An ADC focused biotech in San Diego is currently building out their Clinical Operations team to support their innovative pipeline with therapies ranging from Phase 1-3. As I'm sure you are well aware, ADC's are seen as the future of how we will tackle Cancer in an innovative yet more plausible way compared to other less scalable treatments like Cell Therapy that is still decades away of being accessible to the average cancer patient.

The Clinical Project Manager will provide operational expertise within the Research and Development function to ensure timely initiation, execution, and reporting of clinical trials in accordance with ICH/GCP and all applicable requirements (including local regulations) to support licensure of products in the United States and global markets. This role will work closely and collaboratively with Program Management, Data Management, Clinical Development, Medical Writing, Biostatistics, Clinical Supply, Global Medical Safety, GCP Quality, and Regulatory staff as well as Clinical Research Organizations, to ensure the timely execution of studies within budget. Emphasis will be on superior execution, transparency within the department and to Senior Management, and the ability to employ cost-effective measures and stewardship relative to clinical trial cost projections and final accounting.

Responsibilities (including, but not limited to)

• Independently managing all operational aspects for implementation of clinical trial activities from study start-up through database lock, with expertise in accelerating project launch and site start-up/activations, while ensuring adherence to protocol, GCPs, and relevant SOPs.
• Leading internal cross-functional study teams and partnering with CROs to ensure effective and timely communication, study execution in accordance with the timeline and budget.
• Actively participating in protocol design, CRO selection, site selection, and IRB/EC applications for early and late-phase clinical studies.
• Managing study-related vendors and serving as the primary point of contact for contracted CROs, study staff, and contract labs; identifying potential risks and proactively resolving issues with CROs; establishing vendor management plans and reviewing quality metrics.
• Performing and/or overseeing site monitoring visits for clinical trials as needed.
• Facilitating the timely completion of study protocols (including amendments) and development (and revision) of electronic clinical trial systems (e.g., EDC, IRT).
• Providing input into and/or developing study-related materials such as Clinical Monitoring Plans, Data Management Plans, eCRF forms and completion guidelines, protocols, patient informed consent drafts, site instructions for specimen collections, and study drug order forms.
• Reviewing monitoring reports, protocol deviations, and data listings for sponsored studies to ensure reliable quality data are delivered.
• Coordinating with CROs on site selection, IRB submissions, site initiation, and close-out planning.
• Managing in a timely and efficient manner all operational aspects of protocol amendments.
• Developing and managing reports for communicating study progress and key metrics to Senior Management and program team.
• Coordinating the negotiation of site budgets within guidelines and providing oversight for site payments per contracts.
• Facilitating site study drug orders, and ensuring full drug chain record management, including site accountability records are maintained; managing non-drug supply ordering and tracking, as required.
• Providing oversight and ensuring maintenance of clinical trial master files to ensure their compliance with required regulatory and ICH/GCP quality standards and consistency with SOPs.
• Providing input to Drug (IND) filings, Clinical Trial Applications, safety reports, clinical study reports, and other ICH compliant sections of registration dossiers (e.g., BLA, MAA, NDA, etc.).
• Providing oversight of clinical trials to ensure that all adverse events or product safety issues are captured, reported, and evaluated by appropriate Clinical personnel in a timely manner.
• Establishing a system and procedure for forecasting (and reforecasting) needs for investigational product for each study and communicating those needs on a routine basis.
• Ensuring inspection readiness and participating with CROs and providing support to sites to prepare for clinical audits/inspections and to respond to audit/inspection findings conducted by internal QA and external regulatory agencies.

Qualifications

• Requires a Bachelor's Degree in health or biologic science (BS/BA/BScN or higher); a master's-level degree is preferred.
• A minimum of 5 years of clinical operations experience at a sponsor or CRO, including 1 year as a clinical study lead/project manager is required; global clinical trial experience is required with cardiovascular, rare disease, and/or Phase 1 experience highly preferred.
• Solid, well-grounded experience in setup, execution, and operational management of domestic and international Phase 1, 2, and/or 3 clinical trials across an array of therapeutic areas, including expertise in all aspects of investigational site start-up.
• Effective project management and risk management skills.
• Excellent listening, communication (written, spoken), and interpersonal skills; ability to foster team spirit.