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Clinical Trials Scientific Affairs Supervisor
Rochester Regional Health. Manage daily departmental performance by managing resources, prioritizing tasks, and developing and monitoring metrics .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in managing clinical laboratory operations, including performance management, team development, and process improvement. Proficient in clinical trials coordination and maintaining compliance in a regulated environment.
Highest-signal resume keywords
Clinical Laboratory ExperienceClinical Trials CoordinationMT (ASCP) CertificationPerformance ManagementProcess Improvement
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Laboratory ScienceLaboratory OperationsProject ManagementMetrics DevelopmentTraining DevelopmentSOP UpdatesTesting Method CoordinationPricing Document ReviewReferral Laboratory ContractingTalent Management
Soft Skills
Interpersonal SkillsCommunication SkillsTime ManagementOrganizational SkillsTeam Leadership
Tools & Technologies
Microsoft Office
Certifications & Qualifications
MT (ASCP) Certification
Industry Keywords
Clinical SettingRegulated EnvironmentTalent PlanningEmployee RelationsClient RFPsClient RFIsCross-Functional CollaborationHigh-Performing CultureWorkload ManagementOperational Efficiency
About the role
Key responsibilities & impact- Manage daily departmental performance by managing resources, prioritizing tasks, and developing and monitoring metrics
- Oversee the team’s day-to-day workload
- Hire, coach, and develop direct reports, including role definition, training, development, and performance management
- Facilitate communication and serve as an escalation or strategic contact for the department
- Lead or participate in cross-functional process improvement initiatives
- Promote a high-performing culture through talent planning, selection, onboarding, and continuing education
- Curate and deliver training plans and materials
- Provide coaching, mentorship, performance feedback, and career development plans
- Partner with HR on talent management, performance, employee relations, and development activities
- Investigate clinical trial protocol testing requirements and determine testing facilities
- Review and prepare pricing documents and correct discrepancies
- Maintain relationships with ACM and referral laboratories
- Provide scientific and technical information for client RFPs and RFIs
- Coordinate testing methods with referral laboratories
- Obtain and document referred testing information, including referral laboratory contracting
- Channel information between Laboratory Operations and Sales
- Escalate study, testing, and referral laboratory issues to leadership
- Identify and implement improved work methods to increase efficiency, reduce costs, and solve operational problems
- Liaise with internal and external partners and participate in client teleconferences
- Provide consultation to clinical trials operations and external clients
- Update global SOPs with leadership
- Triage upcoming work and determine staffing capabilities and workload
- Serve as a subject matter expert and escalation point for internal and external clients
- Develop, maintain, and update templates and tools
- Perform other duties as assigned
Requirements
What you’ll need- Bachelor’s degree in a relevant scientific discipline or a minimum of 3 years of experience as a Clinical Laboratory Scientist
- Minimum of 5 years of laboratory experience in a clinical setting, or a relevant regulated environment
- 4 years of clinical trials experience preferred
- Strong interpersonal and communication skills
- Strong time management and organizational skills
- Ability to manage multiple projects with tight deadlines
- Ability to work independently and in a team setting
- Proficient in Microsoft Office
- Generalist laboratory experience
- Ability to lead and positively motivate others
- Models a positive and solutions-oriented mindset
- MT (ASCP) Certification preferred
Benefits
Comp & perks- Full-time schedule
- 37.5 hours per week
- Days, Monday–Friday schedule