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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in programming deliverables within clinical study teams, with strong organizational and documentation skills in a regulated environment. Capable of leading projects, managing resources, and providing performance feedback while collaborating effectively with multidisciplinary teams.
Highest-signal resume keywords
Programming Deliverables LeadershipSAS CertificationRegulated Environment DocumentationPerformance Evaluation InputCross-Functional Collaboration
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Project ManagementData AnalysisQuality ControlDocumentation ManagementComplex Problem Solving
Soft Skills
Clear CommunicationOrganizational SkillsAdaptabilityTeam DevelopmentFeedback Provision
Certifications & Qualifications
SAS Certification
Industry Keywords
Clinical StudyRegulatory ApprovalPerformance EvaluationMultidisciplinary TeamsResource Management
About the role
Key responsibilities & impact- Develop expertise within a therapeutic area or standard tool
- Coordinate and oversee project deliverables independently
- Lead development and quality control of tables, listings, and graphs
- Manage programming effort and track deliverable progress and completion
- Handle complex ad hoc requests
- Serve as programming representative on multidisciplinary study teams
- Support studies through regulatory approval, product launch, and annual reports
- Collaborate with study teams, CROs, and cross-functional colleagues
- Partner with management to determine resource requirements
- Review resumes and screen contractor and permanent role candidates
- Provide feedback on team members' contributions for performance evaluations and goal-setting
- Advise direct reports on data, records, and information-retention procedures
- Contribute to hiring, feedback, and team development
- Maintain rigorous quality and documentation in a regulated environment
Requirements
What you’ll need- Master's degree with 6+ years of relevant work experience, or BS with 7+ years of relevant work experience
- Proven experience leading programming deliverables within a clinical study team
- Experience providing input on hiring, feedback, and performance evaluation
- Strong organizational and documentation skills within a regulated environment
- SAS Certification preferred
- Ability to work onsite in Warren, NJ or Cambridge, MA
- Ability to work with minimal supervision and take ownership of complex deliverables
- Clear communication with cross-functional, multidisciplinary teams
- Analytical and organizational skills for managing multiple priorities and timelines
- Ability to adapt to shifting priorities and last-minute requests
- Right to work and educational qualifications may be verified through background checks
Benefits
Comp & perks- Annual bonuses or other incentive plans
- Equity awards
- Pension or retirement benefits
- 401(k) company match
- Health and wellness programs
- Fitness centers
- Medical, dental, vision, life and disability insurance benefits
- Paid time off
- Family support benefits
- Reasonable accommodation during the recruitment process where required