Clinical Trial Manager PC 1597
About The Position
Your Role: The Clinical Trial Manager drives the clinical trial execution activities for assigned clinical trials, and ensures trial deliverables are met according to timelines, budget, operational procedures, quality standards, GCP, SOPs and business guidelines for Biomedicine, Inc. Miltenyi Biomedicine is a biopharmaceutical company developing personalized chimeric antigen receptor (CAR) T-cell therapies. We are developing innovative treatments for serious life-threatening diseases and are reshaping their accessibility to patients worldwide with the goal of improving and prolonging patients' lives. We are currently focusing on difficult-to-treat hematological cancers using CAR-T and other technologies, while also exploring treatments for other diseases. Our lead candidate, currently in pivotal clinical trials globally, is a tandem CAR T-cell product.
Requirements
- Bachelor’s degree in Life Sciences or similar
- +7 years of clinical research experience at a Biotech/Pharmaceutical or CRO company
- A minimum of 3 years of direct clinical study management experience working in a full service outsource model as a clinical trial manager or clinical project manager is required.
- Global Clinical Trial Experience and the ability to support more than one clinical trial is required.
- Good working knowledge of the international conference on harmonization (ICH) and good clinical practice (GCP) guidelines and other applicable regulatory guidelines required.
- Excellent communication skills, ability to build strong relationships with peers and cross functional team members and CRO/Vendor partners, experience mentoring clinical study staff and presenting to senior management is required.
- Excellent computer skills (Microsoft Office Suite, Project, Word, Excel, PowerPoint, Outlook; Electronic Data Capture Systems)
Nice To Haves
- Experience managing early phase drug development studies is preferred.
- Oncology therapeutic experience is preferred.
Responsibilities
- Provide input to the clinical development plan and operational aspects of the clinical trial protocol (e.g., develops and/or reviews operational plans for trials).
- Lead cross-functional trial execution team to ensure delivery of complex clinical trials and manages protocol execution.
- Identify and/or anticipates operational risks and mitigation plans within assigned clinical trials and escalates issues and recommend contingency plans to Director of Clinical Operations, as necessary.
- Establish study milestones and ensure accurate tracking and reporting of study metrics, timelines, update of trial information in all trial databases and tracking systems.
- Provide monitoring oversight including authoring of oversight plan, reviewing monitoring visit reports and perform periodic oversight visits to sites and/or vendors to assess progress and compliance.
- Manage clinical trial budgets, providing ongoing financial reporting and projections to the finance group and facilitate the development of clinical trial agreements, insurance and other relevant documents in conjunction with legal.
- Ensure the Trial Master File (TMF) is maintained throughout the trial and perform inspection readiness checks throughout the lifecycle of the trial.
- Serve as functional area reviewer of global clinical / regulatory submissions.
- Present study status reports of operational execution activities to senior management.
- Provide study specific mentor and training for in-house Clinical Research Associate(s) and/or Clinical Trial Assistant(s).
- Participate in operational process improvement initiatives (including, training, SOP review and development of work instructions/tools/templates).
Benefits
- The Company offers a comprehensive benefits package, including health, vision, and dental insurance, as well as a 401(k) plan.
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What This Job Offers
Job Type
Full-time
Career Level
Manager
