Clinical Research Coord I

Work Schedule

Environmental Conditions

Job Description

At Thermo Fisher Scientific youll 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.

Summarized Purpose:

Conducts at least one ongoing clinical trial that may involve patients or healthy volunteers. Interacts with the research site team and interdepartmental staff to ensure positive interactions with patients at site for study planning from initiation to closeout.

Essential Functions and Other Job Information:

Conduct clinical studies in strict adherence to FDA/GCP and ICH regulations ensuring patient safety and providing medical care to patients. Perform study activities including informed consent screening and protocol procedures (vital signs pregnancy tests height weight ECGs). Accurately record patient information and test results complete IP accountability logs and report non-compliance. Ensure IRB approval and compliance promote the company and build positive patient relationships. Manage patient bookings follow-up calls and log information on sponsor systems. Gather source documents update patient files and adhere to company standards while maintaining a neat facility appearance.

Bachelors degree or equivalent experience in a clinical/medical field along with a BLS certificate is mandatory. Prior experience (0 to 2 years) demonstrating the necessary knowledge skills and abilities for the role is essential. Consideration will be given to those with a comparable combination of education training and/or directly relevant experience.

Proficiencies and aptitudes:

A basic understanding of clinical research processes including GCP SOPs informed consent and safety monitoring is essential. The capability to work autonomously evaluate data and prioritize intricate information with meticulousness is required. Proven ability to exercise discretion and good judgment along with adequate decision-making negotiation and influencing skills is necessary. Strong communication skills and proficiency in English are advantageous as are excellent organizational skills. Proficiency in basic computer applications and strong interpersonal skills to work effectively in a team environment are also important.

Working Conditions and Environment:

• Work performed in office laboratory and/or clinical environments.
• Exposure to biological fluids and potential infectious organisms.
• Exposure to electrical office equipment.
• Use of personal protective equipment like protective eyewear garments and gloves is required.
• Occasional domestic or international travel.

Physical Requirements:

• Capability to remain in a vertical or fixed position for 6-8 hours daily.
• Repetitive hand movements with the ability to make fast simple repeated movements.
• Frequent mobility required.
• Occasional crouching stooping and frequent bending and twisting of the upper body and neck.
• Ability to lift and carry objects including luggage and laptop computers up to 15-20 lbs.
• Ability to use various computer software applications.
• Strong ability to communicate and understand information and ideas.
• Interact frequently with diverse groups to acquire or relay information.
• Ability to perform under stress and multitask.
• Regular and consistent attendance is essential.