Work Schedule
Other

Environmental Conditions
Office

Job Description

Job Description

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 - To enable 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. Alongside clinical research through our PPD® clinical research portfolio, our work in Accelerated Enrollment Solutions (AES) optimizes each step of the patient journey in clinical trials, such as securing sites and recruiting patients, allowing for more patients to participate in clinical research. Your determination to put patients at the heart of every decision will improve health outcomes that people and communities depend on - now and in the future.

• Carries out clinical evaluation and assessment of participants to ensure eligible participants are recruited and supervised for safety and adherence.
• Attends Site Initiation Visits (SIV), Pre-Selections Visits (PSV) and Investigator meetings as the need arises.
• Participates in recruitment initiatives and strategy development to ensure targets are achieved; ensuring recruiting studies enroll according to plan within timelines and targets.
• Reviews enrolment progress, pre-screening and screening success rates, screen failure rates, safety and retention of participants.
• Interprets protocols and IB.
• Handles and reviews IVRS, CRF/EDC, if applicable.
• Supervises management of investigational medical product (IMP).
• Leads all aspects of multiple studies and/or studies with higher numbers.
• Completes documentation for PI handover.
• Cares for and protects the safety of participants through ethical conduct; this should receive the highest priority at all times during all aspects of the study.
• Fulfills and follows all medical duties, ensuring that clinical trials are performed to acceptable medical, scientific and ethical standards and meet the - requirements as per protocol, SOP/COP ICH and local GCP guidelines and regulations.

• A valid medical degree within the country of practice with at least 2 years working as a licensed physician
• Valid registration as a medical practitioner, with a medical license in good standing and with unrestricted ability to practice in place of work, where applicable
• A valid ICH GCP certificate
• At least 1 year experience working in clinical research with the added advantage of PI responsibility experience, but at least Sub-I experience
• Exceptional general medical practitioner diagnosis and treatment proficiency
• Proficient Polish and English language
• Thorough understanding of medical terminology, drug safety, and interpretation of lab reports
• Proven understanding of scientific concepts related to the design and analysis of clinical trials
• Detailed critical thinking, decision making, analytical and problem solving skills
• Outstanding communication skills and ability to work with a cross-functional team to get results
• Demonstrated ability to influence and collaborate at all levels throughout the organization
• Excellent written, verbal and presentation skills
• Capable of working well under pressure
• Capable of effectively prioritizing and handling multiple projects
• Strong planning, organizational and project management skills
• Capable of handling outside agencies in order to fulfill project objectives
• Self-starter with ability to thrive under pressure in a fast paced environment
• Skilled in working with MS Office and Internet