About the position
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future. Our dedicated early phase clinical trials team, within the PPD™ clinical research business of Thermo Fisher Scientific, consists of global experts in early development and clinical pharmacology. With our extensive facilities, site network, operational expertise, and development experience, we specialize in developing integrated, early-phase programs that efficiently conduct trials involving both patients and healthy volunteers.
Responsibilities
- Coordinates global site identification assessments and provides updates to all global participants as required.
- Coordinates programming and validation of feasibility surveys according to the timeline, quality standards and client expectations.
- Provides matrix management of internal team members in site identification assessments, identification of risks and development of mitigation plans.
- Prepares global site identification data analysis and formal progress reports (including narratives) within established timelines.
- Participates in alternative clinical intelligence gathering initiatives as alternatives to survey drive site identification assessment.
- Responds accurately to department email and telephone inquiries from internal and external clients.
- Assists with additional department objectives and projects as necessary.
Requirements
- Experience in clinical research or related field.
- Strong analytical and problem-solving skills.
- Excellent communication and interpersonal skills.
- Ability to manage multiple tasks and projects simultaneously.
- Proficiency in data analysis and reporting.
Nice-to-haves
- Familiarity with clinical trial processes and regulations.
- Experience with feasibility assessments and site identification.
Benefits
- Health insurance coverage.
- 401k retirement savings plan.
- Paid holidays and vacation time.
- Professional development opportunities.
