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Project Manager, I-Labs
Thermo Fisher Scientific. Liaise with PPD operational departments, affiliates, and sponsors .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates strong project management capabilities, with a focus on coordinating clinical study activities, maintaining compliance with procedural documents, and ensuring effective communication with clinical teams and sponsors. Possesses a solid understanding of clinical trial processes and the ability to manage study setups and modifications efficiently.
Highest-signal resume keywords
Project ManagementClinical Trial ProcessesBudget MonitoringCommunication SkillsProblem-Solving Skills
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 CoordinationBudget ManagementProtocol AmendmentsStudy SetupTechnical Problem Resolution
Soft Skills
Attention to DetailOrganizational SkillsTeam CollaborationOral Presentation Skills
Tools & Technologies
Project Management SoftwareClinical Trial Management Systems
Certifications & Qualifications
Bachelor's Degree
Industry Keywords
Clinical TrialsStudy MaintenanceConfidentialityLaboratory EnvironmentPersonal Protective Equipment
About the role
Key responsibilities & impact- Liaise with PPD operational departments, affiliates, and sponsors
- Coordinate study setup, maintenance, and closure activities for identified protocols and/or study programs
- Serve as local study coverage for global studies and point of contact for Clinical teams
- Ensure timely completion of study activities and deliverables
- Document communications and actions with sponsors or investigator sites
- Manage existing Batch, Supply Only, and “In Conduct” studies
- Develop new study setups in collaboration with the Tech Ops group
- Provide backup coverage for Project Management staff and Project Managers
- Advise Project Managers on procedural and budgetary items and study modifications or protocol amendments
- Monitor monthly Budget-to-Burn reviews and contract modifications
- Support initial study supply orders, templates, and shipment requests
- Monitor completion of shipment requests
- Schedule internal and external meetings and teleconferences; prepare agendas and distribute minutes
- Monitor assignments, adjust priorities and work schedules, and complete additional project, client, and departmental tasks
Requirements
What you’ll need- Bachelor's degree or equivalent and relevant formal academic / vocational qualification
- Previous experience comparable to 0 to 2 years’ or equivalent combination of education, training, & experience
- Good organizational, project management, and computer skills
- General knowledge of clinical trial processes and programs
- Strong attention to detail and problem-solving skills
- Good written and verbal communication skills
- Ability to effectively conduct oral presentations
- Experience identifying and resolving technical problems in a lab environment
- Ability to maintain confidentiality with clinical teams
- Ability to attain, maintain, and apply working knowledge of applicable procedural documents
- Ability to work well with others
- Ability to work in laboratory and/or clinical environments and use required personal protective equipment
- Occasional drives to site locations and occasional domestic travel
Benefits
Comp & perks- Health and wellbeing support
- Healthy and balanced work environment
- Collaboration and development opportunities
- Personal protective equipment provided/required for workplace safety
- Occasional domestic travel