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Manager, Research & Development

Job in City of Rochester, Rochester, Monroe County, New York, 14602, USA
Listing for: Rochester Regional Health
Full Time position
Listed on 2026-02-06
Job specializations:
  • Management
    Healthcare Management
  • Healthcare
    Healthcare Management
Job Description & How to Apply Below
Location: City of Rochester

Job Title: Manager, Research & Development

Department: Research & Development

Location: Onsite,160 Elmgrove Park Rochester, NY

Hours Per Week: 40

Schedule: Days

Position Summary

The Manager, Research & Development leads, manages and coordinates all R&D activity, reporting to the Scientific lead or VP clinical trial laboratory operations. Responsible for liaising with the Principal Scientist and laboratory operations to coordinate scientific strategy laboratory requirements, validations, SOPs, trouble shooting and training, as required. Ensures all documentation is appropriate for the regulatory environment. Oversees and directs all R&D client interaction and external (third party) laboratory interaction for the R&D team coordinating the development of 3PL and client strategies and meetings.

Ensures R&D processes are effective and oversees the pre-award and post- award support.

Key Responsibilities
  • Maintain daily departmental performance by managing resources, prioritizing tasks, and developing and monitoring metrics.

  • Facilitate communication as a point of escalation or strategic point of contact for the department.

  • Identify, lead, and/or participate in cross functional process improvement initiatives to optimize operational capabilities.

  • Promote and uphold a high performing culture through effective talent planning, selection, onboarding and continuing education.

  • Curate and deliver comprehensive training plans and materials to foster successful onboarding and employee performance.

  • Provide ongoing coaching and mentorship supported by routine performance metrics to identify clear performance feedback and career development plans.

  • Foster professional development through continuous coaching and performance management

  • Works with Principal Scientists and VP lab ops to support R&D and operations for strategic initiatives including new biomarkers and technologies.

  • Creates plan for conference attendance and external marketing.

  • Manage client programs and strategic initiatives in collaboration with the laboratory and other cross-functional departments.

  • Assigns R&D team and supports team with Clients and 3PLs for oversight of haematology and chemistry and pharmacodynamic (PD) analysis.

  • Coordinate and lead R&D team through the coordination of marketing material related to scientific strategy across all service lines and strategic initiatives

  • Accountable for design and execution of all clinical trials method validations in collaboration with operational teams and Principal Scientists

  • Ensures all methods and validations are done according to all applicable regulatory guidelines, including but not limited to Good Clinical Practice (GCP), Good Laboratory Practice (GLP), Good Clinical Laboratory Practice (GCLP), College of American Pathologists (CAP) NYSH / UK EMEA.

  • Responsible for ensuring teams are trained and compliant with all regulations as appropriate.

  • Manage and coordinate change control activities relating to technologies.

  • Liaise with QA to complete internal and external audit findings.

  • Coordinate trouble-shooting activities with laboratory operations and Principal Scientists

  • Coordinate and responsible for execution of scientific support of internal and external partners based on challenges and new technologies)

  • Oversee the harmonisation of global SOPs process as appropriate

  • Works with Principal Scientists and oversees 3PL relationships for R&D team.

  • Coordinates the development of 3PL and Client strategy and attends meetings as appropriate.

  • Ensures process of supporting pre award is effective and works with the Principal Scientists to suggest new testing requirements in line with client requests and the scientific strategy.

  • Coordinates the translation of the analytical strategy into operational plans.

  • Plans the initiation and oversees the execution of validations as appropriate.

  • Oversees method onboarding activities in a suitable timeframe to support clinical trials activities as appropriate with support of Principal Scientists.

  • Perform other duties as needed.

Minimum Qualifications
  • BS in Life Sciences
  • 7 years in central laboratory or CRO experience including 2 years of supervisory or leadership experience
Preferred Qualifications
  • PhD…
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