**Work Schedule** Other **Environmental Conditions** Office **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 - 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. **Location/Division Specific Information** Our Early Development team focuses on Phase I and IB trials which represent the first practical tests of a compound’s clinical relevance and commercial viability. They are the culmination of years or even decades of research. Moreover, they set the stage for subsequent studies that will ultimately determine your compound’s efficacy, safety and positive impact on patient’s lives. **Discover Impactful Work:** Collaborates with multidisciplinary teams to ensure successful execution of clinical research protocols according to the organization's SOPs, GCP and EMA/ICH guidelines. This role involves high-quality subject care, data collection and educating patients and their families about treatments and possible side effects of study medication. **A day in the Life:** + Reviews protocols for scientific, logistical and safety feasibility. + Conducts specific roles and responsibilities for specialized studies requiring expert nursing experience in a therapeutic area. + Ensures the trial is conducted under the requirements relating to informed consent and Ethical requirements. + Performs appropriate clinical procedures which may include, but are not limited to: vital signs, blood collection, IV starts and infusions, investigational product administration, monitoring biopsy sites and removal of sutures, and safety assessments. + Attends internal meetings related to logistics, training and client meetings to discuss scientific and medical oversight of a particular protocol or the clinic in general. + Attends internal/external training related to licensure and medical malpractice requirements and trains staff on new procedures and processes. + Reviews and consults with clients on new or ongoing projects within the clinic and with the investigator group on scheduling and study assignments. **Keys to Success:** **Education and Experience:** Diploma from a higher professional school with degree in general nursing or bachelor's degree in nursing. Completes continuing educational requirements timely. **Knowledge, Skills and Abilities:** + Excellent understanding of the clinical research process (i.e., GCP, SOPs, informed consent, safety monitoring, etc.) + Capable of working independently, analyzing and working with attention to detail, processing and prioritizing sensitive complex information and problem solving + Demonstrates ability to exercise discretion and sound judgement + Excellent decision-making, negotiation and influencing skills + Excellent communication skills with Czech and English level A2 or B1 + Excellent organizational skills + Essential proficiency in basic computer applications + Excellent interpersonal skills to work in a team environment **Work Environment** + Work is performed in an office/ laboratory and/or a clinical environment. + Exposure to biological fluids with potential exposure to infectious organisms. + Exposure to electrical office equipment. + Personal protective equipment required such as protective eyewear, garments and gloves. + Occasional travel, may be domestic or international. + Continuous working regime required (24/7) with fixed weekly 37.5 working hours according § 79 paragraph 2 letter b) of the Labor Code (hours scheduled per shift plan Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.