O pozici
Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Conducts all clinical trials (studies) according to ICH GCP, local regulations, study protocol and company processes. Ensures the medical wellbeing and safety of the participants through the safe performance and execution of the studies. Maintains clinical oversight and quality on the studies registered on and delivers on study targets, thereby contributing to the commercial success of the site which includes: recruitment, enrolment and retention of study participants. This will be working on a DCP contract - maximum 20 hours per week
Co budeš dělat
- Carries out clinical evaluation and assessment of participants to ensure eligible participants are enrolled onto studies.
- Reviews enrollment progress, pre-screening and screening success rates, screen failure rates, safety and retention of participants.
- Interprets protocols and IB and participate in initiatives to strategize for patient recruitment.
- Ensures and protect the welfare and safety of participants through ethical conduct; this should receive the highest priority at all times during all aspects of the study.
- Fulfills and comply with all medical duties as per protocol, SOP/COP and ICH GCP and local regulations.
- Reports any safety threats, that may impact stakeholders/participants and action complaints or QIs as per site processes.
- Exercises meticulous attention to detail in recording information and source management.
- Actively involved in audit preparations and site inspections.
- Oversees the management of investigational medical product (IMP).
Koho hledáme
- A valid medical degree and registration within the country of practice
- A medical license in good standing, with unrestricted ability to practice in place of work, where applicable
- A valid ICH GCP certificate
- No previous experience in clinical research years of required, but must have general medical practitioner diagnosis and treatment proficiency
- In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
Benefity
- Thank you for your interest as you consider starting a new career journey with us. As the world leader in serving science, our colleagues develop critical solutions through innovation—and build rewarding careers. Discover their extraordinary stories and connection to our Mission to enable our customers to make the world healthier, cleaner and safer. Their work is a story of purpose. What story will you tell?
- Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of more than $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD.
- We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
- Thermo Fisher Scientific is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, creed, religion, color, national or ethnic origin, citizenship, sex, sexual orientation, gender identity and expression, genetic information, veteran status, age or disability status.
