Sr. Clinical Trial Manager Contractor (6 months)

Sr. Clinical Trial Manager

This is an exciting opportunity to work within a fast-paced environment with a dedicated, passionate, intelligent team. As a Sr. Clinical Trial Manager, you will be responsible and accountable for managing operational activities for assigned studies and may assume responsibility for additional vendors, studies and / or clinical programs, as they become available. The Sr. Clinical Trial Manager provides operational leadership to ensure the study milestones are delivered on time, within budget, with high quality, and in compliance with the ICH / GCP, Regulatory Authorities' regulations / guidelines, and applicable SOPs. The Sr. Clinical Trial Manager will help establish new processes and work instructions to ensure consistent, effective, and efficient execution of clinical operation activities. The Sr. Clinical Trial Manager will partner with key stakeholders (internal and external) to ensure continuous harmonized operations of clinical operations activities and to maintain high standards for performing in a cross-functional environment. The Sr. Clinical Trial Manager may also manage junior staff members as well as develop and participate in departmental training and annual review processes. This role is on-site at least 3-days a week.

Essential Responsibilities :

• Assume responsibility and management of clinical trial as a Study Lead to ensure that corporate goals are met, studies are completed on time, within budget, and in compliance with SOPs, FDA / EMA regulations and ICH / GCP guidelines.
• Responsible for study start-up, including working with cross functional teams on startup, and with the CRO on site selection / activation.
• Act as the study lead on cross-functional study teams, Vendor, and CRO operational meetings and ensure compliance with global operational standards and procedures.
• Support vendor selection, onboarding, management, and oversight of multiple vendors including but not limited to CRO (including RFPs and bid defense for CRO and finalization of SOW), imaging, central and specialty labs, eCOA, and compliance.
• Manage vendor operational meetings to ensure project goals and timelines are met.
• Assist with or be responsible for the management of key study parameters (e.g., start-up activities, site feasibility, enrollment, site management, data collection, data review, database lock, etc.) and proactively identify solutions within the clinical team when issues arise.
• Participate in the development and review of study related materials, including but not limited to informed consent forms, case report forms, study manuals and plans, and other supporting clinical trial materials.
• Create study specific tools and manuals to ensure timeliness, standardization, and control of data quality.
• Assist with the analysis and development of action plans to address issues with investigational sites and / or vendors.
• Responsible for the review and oversight of tasks in study management plans for operations and all operational activities associated with clinical trials.
• Review / approve invoices, and ensure timely payment processing for vendors, including investigative sites (as applicable).
• Ensure inspection-readiness for all assigned studies, including ensuring all components of the trial master file (TMF / eTMF) are up to date and accurate.
• Assist with the planning, coordination, and presentation at Investigator Meetings and CRA Training meetings, SIVs, and ad hoc trainings, as requested.

Education / Experience :

Given the "small biotech" nature of the Company, cultural fit of the successful candidate is an important criterion for their success at Biomea Fusion. Desired characteristics include a high level of curiosity, intelligence, ability to work independently, "can do" attitude, and an entrepreneurial spirit. Strong initiative and follow through are essential for this job.

BA required, preferable in a scientific / medical field. Advanced degree preferred. At least 8-10 years of experience in Clinical Operations or related function, working with CROs and other vendors, with increasing responsibility and scope. Working knowledge of FDA / EMA regulatory requirements and ICH / GCP guidelines. Previous experience working in cross-functional environment. Demonstrated experience in selecting, managing, overseeing, and successfully developing effective relationships with multiple vendors and CROs. Proficiency with Microsoft applications. Prior experience working in a start-up environment is a highly desired.

Specific Qualifications Include :

Industry : Biotechnology

Employment Type : Contract - $125 / hour depending on experience.

Equal Employment Opportunity :

At Biomea Fusion, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer, we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic.