| Clinical Research Manager :: Onsite Lawrenceville, NJ :: No H1B-CPT at Lawrenceville, Virginia, USA |
| Email: [email protected] |
| From: Priya, KPG99 [email protected] Reply to: [email protected] Clinical Research Manager Onsite: Lawrenceville, NJ. No H1B/CPT Duration: 12+ months. What we need to submit: * Resume with full education details. * Photo ID * Current Location Zip Code. * Updated LinkedIn. * Great communication skills. Industry experience Required: Pharma, Biotech, CRO Position Summary: This individual contributor role has task-level responsibility for in-house and outsourced studies while ensuring adherence to the client's outsourcing strategies within a specific therapeutic area(s) and is accountable to support clinical trial vendor partnerships across select or multiple service categories of clinical trial activities in R&D. Key Responsibilities: Drive outsourcing activities by interfacing with operational teams, support groups and service providers for successful selection, contracting and execution of outsourced studies while ensuring compliance with regulatory standards, ethical practices, outsourcing and procurement policies and procedures Drive the success of projects to meet short-term objectives & adhere to project schedules Support Outsourcing team in a variety of tasks across outsourcing, alliance management, FSP operations and Financial/ Resource accountability Communicate with business partners and internal clients regarding contractual issues as needed Provide operational expertise and support, guidance and training to teams on all aspects of outsourced work Ensure alignment of teams to the related BMS outsourcing strategies Qualifications & Experience: Minimum of a BA or BS Degree in Legal, Life science, Business Administration or equivalent. Advanced degree a plus. Clinical development experience of 3 to 5 years of relevant industry experience (pharma, biotech, CRO) required. Experience engaging with a wide range of suppliers (e.g., Contract Research Organizations, Cooperative groups, Clinical laboratories, Core laboratories including ECG and Imaging service providers): initiating, negotiating and executing legal and/or financial agreements in the clinical trials environment- biotech or pharmaceutical industry. Proven experience in managing key internal and external stakeholders effectively by frequently soliciting input and gathering and incorporating feedback into processes as appropriate. Effective management of cross-functional, multi-cultural teams and demonstrated ability to work and influence within a matrix structure. Keywords: business analyst rlang Idaho New Jersey Clinical Research Manager :: Onsite Lawrenceville, NJ :: No H1B-CPT [email protected] |
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| Wed May 15 22:31:00 UTC 2024 |