Project Manager, Medical Device

1 week ago


San Diego, United States Pharmaron Full time

Position: Project Manager Department: Medical Device FLSA status: Exempt Location: Carlsbad, CA Position Description: We are looking for a highly motivated and experienced Project Manager to join our team. As a Project Manager for Medical Device Specialty In Vivo Services at Pharmaron, you will play a pivotal role in driving our business growth and establishing our leadership in the industry. Your primary focus will be on coordinating scientific account management for our specialized preclinical testing services for our scientific partners and companies developing medical devices, for cardiovascular, metabolic, ocular, dermal, or CNS applications. Key Responsibilities: Cultivate a deep understanding of Pharmaron's medical device testing workflow, enhance familiarity with the regulatory requirements for safety and biocompatibility assessments of medical device products. Enhance knowledge of departmental capabilities, general surgical procedures, equipment, and standard operating procedures. Project Planning: Independently develop and manage project plans, ensuring alignment with regulatory standards and departmental capabilities. Proposal Development: Create compelling study proposals, including budgets and detailed project scopes. Client Communication: Maintain effective communication with clients, providing regular updates and addressing inquiries. Regulatory Compliance: Ensure projects adhere to relevant regulatory requirements for medical device research. Collaboration: Collaborate with cross-functional teams to ensure seamless project execution. Risk Management: Proactively identify and mitigate project risks. Documentation: Maintain accurate and comprehensive project documentation. Qualifications: Advanced degree (Master's or higher) in biological science, with a focus on anatomy, cardiovascular system, dermal, and neuroscience. Direct experience in the field can be considered in lieu of the education requirement. Proven experience in project management, preferably in the medical device industry and/preclinical CRO. Strong understanding of regulatory requirements for medical devices. Ability to independently draft study proposals, budgets, and project scope of work. Excellent organizational and multitasking skills. Effective communication skills for client interactions. Motivation to learn and adapt to evolving industry trends. Benefits: Pharmaron cares about our work community and offers a variety of benefits allowing employees the opportunity to customize a benefits package that meets their personal needs. Company benefits include the following: Medical, Dental & Vision Insurance Plan with Employer Contribution Health Reimbursement Account Funded by Employer Healthcare & Dependent Care Flexible Spending Accounts Employee Life and AD&D Insurance 100% Employer Paid Voluntary Life and AD&D Insurance for Employee, Spouse & Child(ren) Short and Long Term Disability 100% Employer Paid 401k with Employer Match Employee Assistance Program Pharmaron is proud to be an Equal Employment Opportunity and Affirmative Action employer. About Pharmaron Pharmaron (Stock Code: 300759.SZ/3759.HK) is a premier R&D service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities, and established a broad spectrum of research, development and manufacturing service capabilities throughout the entire drug discovery, preclinical and clinical development process across multiple therapeutic modalities, including small molecules, biologics and CGT products. With over 19,000 employees, and operations in China, the U.S., and the U.K., Pharmaron has an excellent track record in the delivery of R&D solutions to its partners in North America, Europe, Japan and China. Pharmaron is proud to be an Equal Employment Opportunity and Affirmative Action employer.

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