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Posted: 10/19/2026Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in coordinating and executing observational research studies while ensuring compliance with Good Pharmacoepidemiology Practice and CORE SOPs. Proficient in project management, data integrity, and collaboration with cross-functional teams to drive clinical deliverables.
Highest-signal resume keywords
Observational Research CoordinationGood Pharmacoepidemiology Practice ComplianceProject ManagementEpidemiologic Research KnowledgeStakeholder Collaboration
Tech Stack
Tools & technologiesAbout the role
Key responsibilities & impact- Lead operational activities related to study planning, study execution, and summarization of results from observational research studies
- Coordinate the end-to-end execution of observational or non-interventional research studies in compliance with Good Pharmacoepidemiology Practice and CORE SOPs
- Plan, initiate, execute, and close out primary data collection, chart review, database, molecular epidemiology, literature review, dossier development, and economic modelling activities
- Collaborate with CORE, Global Medical and Scientific Affairs, and lead scientists to support study conduct
- Provide study-level management support for proposals, scopes of work, agreements, amendments, and change orders
- Participate in protocol and interim/final report preparation and literature review abstraction and summarization
- Coordinate review and finalization of vendor documents and track study timelines, deliverables, milestones, and action items
- Troubleshoot issues with internal and external partners and liaise with outsourced vendors and cross-functional teams
- Participate in quality control assessments and ensure study data integrity for reports and publications
- Coordinate and document adherence to internal, external, and regulatory compliance requirements
- Utilize, manage, and maintain document repositories and internal/external systems including REV OPS, Engage Zone, and Veeva Vault
- Support due diligence checks, site contract and budget review/approval, informed consent, study registration, IT/privacy assessments, vendor qualification, adverse event reporting and reconciliation, and publication submissions
- Manage poster and publication development, including formatting, medical writing, figure/data content development, co-author review, and internal review
Requirements
What you’ll need- Two or more years of work experience within clinical/observational research or equivalent experience
- Excellent communication and interpersonal skills and the ability to collaborate with and influence a wide variety of stakeholder
- Basic knowledge of epidemiologic or outcomes research
- Fluency in English (written and spoken)
- Strong project management and prioritization skills
- High level of motivation and ability to work independently and collaboratively
- University degree in medicine, science, or equivalent combination of education & experience
- Demonstrated ability to drive the clinical deliverables of a study
- Subject matter expertise in the designated therapeutic area
- Prior monitoring experience is preferred
- Willingness to travel as required (approximately 25%)
- Legal right to work in the country where the role is based
Benefits
Comp & perks- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Study PlanningData CollectionDatabase ManagementEconomic ModellingMedical WritingQuality Control AssessmentProtocol PreparationLiterature ReviewVendor ManagementAdverse Event Reporting
Soft Skills
Excellent CommunicationInterpersonal SkillsCollaborationInfluencing StakeholdersMotivation
Tools & Technologies
REV OPSEngage ZoneVeeva Vault
Industry Keywords
Clinical ResearchObservational StudiesTherapeutic Area ExpertiseRegulatory ComplianceMonitoring Experience