FREE ACCESS
5,000–10,000 jobs/day
See all jobs on Scoutfield
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in global clinical trial management, ensuring compliance with ICH-GCP and regulations while delivering high-quality studies on time and within budget. Strong collaboration and communication skills are essential for working with cross-functional teams and stakeholders in the cardiovascular therapeutic area.
Highest-signal resume keywords
Global Trial Management ExperienceClinical Development KnowledgeICH-GCP ComplianceProject Management SkillsStakeholder Management
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 ResearchPharmaceutical DevelopmentBiotechnologyCardiovascular Clinical TrialsStudy Protocol DevelopmentStudy Close-OutBudget ManagementRegulatory ComplianceProject ManagementOrganizational Skills
Soft Skills
CollaborationCommunicationProactivityIndependenceTeamwork
Industry Keywords
Life SciencesMedical SciencesBiological SciencesCRO EnvironmentGlobal Clinical TrialsCross-Functional TeamsFast-Paced Environment
About the role
Key responsibilities & impact- Support delivery of global clinical studies from protocol development through study close-out and archiving
- Collaborate with internal stakeholders, CROs, and external vendors on a global level
- Ensure studies are delivered on time, within budget, and to high quality and compliance standards
- Support innovative programmes, including global cardiovascular clinical trials
- Work as part of a cross-functional global study team
- Contribute to clinical research programmes and studies within the cardiovascular therapeutic area
Requirements
What you’ll need- Degree qualified in Life Sciences, Medical Sciences, Biological Sciences, or a related field
- UK based
- 3+ years of Global trial management experience in clinical research, pharmaceutical development, biotechnology, or a CRO environment
- Strong understanding of clinical development and the drug development process
- Excellent knowledge of ICH-GCP and global clinical trial regulations
- Proven project management and organisational skills
- Strong stakeholder management and communication skills
- Experience working effectively within global, cross-functional teams
- Previous experience supporting cardiovascular clinical trials is highly desirable
- Proactive, collaborative, and able to work independently in a fast-paced environment
- 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