Director of Clinical Operations


About

They will be responsible for all aspects of study conduct and CRO oversight and is the primary point of contact for clinical study project management, communications, and will assume a high level of decision-making authority. Experience and knowledge of end-to-end management of clinical trial conduct, knowledge of the pharmaceutical industry and an understanding of clinical drug development, clinical trials operations and regulatory components is essential. Essential Functions Specific Job Functions/Responsibilities: • Ability to manage complex protocols within a matrix environment. • Experience in working with and overseeing Contract Research Organizations (CROs) and other external vendors is required. • Demonstrated ability to drive clinical trial activities: i.e. experience in all aspects of study start-up and conduct, regulatory obligations, adverse event reporting, budgeting. • Manage all clinical aspects of the study, including responsibility for oversight of study execution, develop and manage comprehensive study timelines and metrics; management/oversight of external vendor deliverables reports and budgets. • Report on all aspects of the study progress to MMRC/F management • Provides study-specific training and leadership to clinical research staff, including CRO, sites and other contract personnel. • Provide leadership and serve as the clinical trial subject matter expert. • Oversees the following groups across the trial program: CRO, clinical supplies, DM, outsourcing and vendor alliance management. • Primary contact for MMRC’s Pharma Partners. • Ensure Pharma Partner trial reporting requirements are being met. • Prepare and present project reports as required. Plans, executes, and leads study-specific meetings as needed (e.g., Study Management Meetings, site calls etc.). • Study budget management and oversight of vendor and site payments. Liaise with MMRF’s finance group on budget expense projections and payment reconciliation. Review and approve clinical invoices against approved budgets. • Ability to identify and manage or escalate risks. • Review and sign off on monitoring reports, ensure study issues and action items are addressed and closeout appropriately and in compliance with study management plans. • Daily interaction with study CRO project manager, the MMRC medical monitor and other members of the cross-functional study team. • Prepares and/or reviews study-related documents (e.g., Study Operations Plan, Monitoring Plan, Pharmacy Manual, Informed Consent, Laboratory Manual, CRF Completion Guidelines, study tools/ worksheets and other study-specific documents or manuals). • Provide input on operational components of legal documentation and statements of work as required for new and returning sponsors, vendors and suppliers. • Write and review study protocols, informed consents and amendments. Director of Clinical Operations Job Description Qualifications • Bachelor’s Degree (BA, BS) in scientific or health care discipline preferred. • Minimum of 10 + years of relevant experience; ideally a combination of pharmaceutical, biotech and/ or CRO-related oncology clinical research experience. • Oncology experience required; Hematology oncology therapeutic experience strongly preferred. • Excellent organizational skills, ability to manage multiple tasks and meticulous attention to detail. • Effective oral, written and interpersonal communication skills. • Computer literacy required (MS word, MS excel, MS PowerPoint and MS Project) • CRO oversight experience • Experience working in (CRO/Pharma) required • Demonstrated ability to multi-task and manage high performance demands • Strong leadership and supervisory skills • Strong organizational skills • Ability to travel as necessary (approximately 10%) • Excellent working knowledge GCP, FDA and ICH Guidelines. Ensures the assigned clinical trials are executed in compliance with FDA and ICH GCP guidelines/regulations and SOPs. • Comfortable multi-tasking in a fast-paced small company environment and able to adjust workload based upon changing priorities. • Excellent team player; willingness and ability to fill functional gaps in a small organization. • Preference to energetic candidates with a desire to think “outside the box”. Essential Functions Specific Job Functions/Responsibilities (cont.): Qualifications This is a non-profit organization. Send CV/Resume to: hr@themmrf.org The MMRF/C is an equal opportunity employer. All employment decisions are made without regard to race, color, age, gender, gender identity or expression, sexual orientation, marital status, pregnancy, religion, citizenship, national origin/ancestry, physical/mental disabilities, military status or any other basis prohibited by law. EOE, M/F/D/V

Where

Norwalk, Connecticut
United States

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