Senior Clinical Project Manager, RWE
Syneos Health
full-time
Posted on:
Location Type: Remote
Location: Spain
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Job Level
Tech Stack
About the role
- Manages a project as a Project Manager overseeing interdisciplinary clinical research studies and/or programs and ensures compliance with GCP, relevant SOP’s and regulatory requirements
- Acts as primary liaison and/or facilitator between the Company and the Customer to ensure project launch, conduct, and closeout according to the Customer’s and the Company's contractual agreement
- Leads project team to ensure quality, timelines and budget management
- Implements resource strategies to achieve project goals
- Accountable for all project deliverables for assigned projects
- Develops contingency planning and risk mitigation strategies to ensure successful delivery of study goals
- Identifies and implements performance improvement and operational efficiencies
- Maintains and evaluates project progress by maintaining timelines, project plans and other tracking/analysis tools
- Produces and distributes status, resourcing, and tracking reports as well as functional area plan to customers, appropriate team members and senior management
- Maintains effective communication with the Customer and project team through oral and written correspondence, project status reports, and monthly progress reports
- Attends and presents information at internal and external project meetings
- Develops strong relationships with current and prospective clients to generate new and/or add-on business for the future
- Supports the Business Development Department by providing information on Company's capabilities, patient populations, etc. and presents Company capabilities as well as project management specific responsibilities at Customer proposal defense meetings
- Works with Business Development and the Proposal/Contracts groups to develop proposals for Customer requested opportunities
- Responsible for quality and completeness of TMF for assigned projects
- Accountable for the financial performance of each project assignment
- Accountable for maintenance of study information on a variety of databases and systems
- Responsible for study management components of inspection readiness for all aspects of the study conduct
Requirements
- Bachelor’s Degree (or equivalent) level of qualification in life sciences, Medicine, Pharmacy, Nursing or equivalent combination of education and experience
- Ideally Project Management qualified i.e. Prince II or PMP / equivalent
- Strong knowledge of Good Clinical Practice/ICH guidelines, regulatory requirements, drug development process and clinical monitoring procedures
- Strong organizational and time management skills
- Clinical research organization (CRO) and relevant therapeutic experience preferred
- Ability to embrace new technologies
- Excellent communication, presentation, and interpersonal skills, both written and spoken, with an ability to inform, influence, convince, and persuade
- Ability to travel as necessary (approximately 25%)
Benefits
- career development and progression
- supportive and engaged line management
- technical and therapeutic area training
- peer recognition
- total rewards program
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard skills
project managementrisk mitigationresource managementperformance improvementclinical monitoring proceduresstudy managementfinancial performance managementcontingency planningtimelines managementtracking and analysis tools
Soft skills
communication skillspresentation skillsinterpersonal skillsorganizational skillstime management skillsrelationship buildinginfluencing skillspersuasion skillsteam leadershipclient management
Certifications
Bachelor’s Degree in life sciencesPrince IIPMP