Regional CRA Supervisor - East Coast (remote with travel)
At TE, you will unleash your potential working with people from diverse backgrounds and industries to create a safer, sustainable and more connected world.
Job Overview
What your background should look like:
Competencies
The Regional CRA Lead/Supervisor responsible for the functional line management, coaching and mentoring of a regional team of Clinical Research Associates (CRAs). This role is instrumental in building and managing high performing teams which support the efficient and effective execution and delivery of clinical studies.
Responsibilities:
Recruit, train, develop, and supervise assigned Clinical Research Associate team
Screen new contract and FTE candidates, arrange interview teams and debriefings, make hiring decisions
Contribute to team curriculum and onboarding plan maintenance and improvement
Onboard, train, coach, mentor, and advocate for direct reports in job responsibilities, company culture, and career goals
Identify training needs, formulate strategies to address training gaps, and conduct training
Evaluate ongoing performance and perform performance reviews of assigned staff.
Develop and maintain effective relationships with study and management teams as well as the cross-functional relationships with which CRAs interact to optimize feedback
Contribute to the planning of resource allocations to clinical studies and other Clinical Development Operations activities
Contribute to Clinical Development Operations quality, systems, and process initiatives.
Support day to day operational activities of the team in partnership with other line managers and Team Manager(s)
Serve as CRA on assigned studies
Contribute to preparation and follow-up of sponsored quality audits, as well as regulatory authority inspections
Perform all duties and responsibilities in accordance with CFR, GCP/ICH, and other applicable guidelines
Help create a fun, rewarding, and collaborative environment
Education/Skills:
Minimum of Bachelor's Degree in life science or related field preferred
Minimum of 5 years of relevant experience with at least 2 years of experience in the pharmaceutical/biotech company or CRO.
Prior experience managing a team with three or more team members.
Demonstrated working knowledge of GCP, ICH guidelines, and FDA regulations.
Excellent oral and written communication skills and strong organizational abilities.
Ability and willingness to travel up to 50% of the time.
COMPENSATION
• Competitive base salary commensurate with experience: $90,000–130,000 (subject to change dependent on physical location)
• Posted salary ranges are made in good faith. TE Connectivity reserves the right to adjust ranges depending on the experience/qualification of the selected candidate as well as internal and external equity.
• Total Compensation = Base Salary + Incentive(s) + Benefits
BENEFITS
• A comprehensive benefits package including health insurance, 401(k), disability, life insurance, employee stock purchase plan, paid time off and voluntary benefits.
EOE, Including Disability/Vets
remote, NC, US, -
Job Segment:
Drafting, Electrical, Testing, Fabrication, Engineering, Technology, Manufacturing, Quality