Clinical Research Coordinator

Thermo Fisher Scientific • Melbourne, FL

1d • Onsite

About The Position

Join us as Clinical Research Coordinator - And manage the day-to-day operations of our clinical trials. What You’ll Do: Conduct multiple ongoing clinical trials, of varying size and complexity, involving patients or healthy volunteers/subjects. Complete all paperwork required to capture all data as specified by a study protocol, and for ensuring subject safety, understanding, and cooperation during the study process. Interact with the research site team and other interdepartmental staff. Engage in the entire site operations process, which includes recruitment, enrollment and retention of study participants. May act as primary or lead CRC on certain studies, taking the overall responsibility thereof at the site, while maintaining communication and updates with site team, liaising with monitors and other stakeholders.

Requirements

• Relevant formal academic / vocational qualification and/or previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 5 years).
• 1+ year of leadership responsibility.
• 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.
• Fundamental communication and interpersonal skills with the ability to manage, motivate and mentor staff
• Strong organization skills with ability to handle multiple tasks simultaneously, meet rigorous timelines and work effectively in stressful situations
• Understanding of budgets, project planning and performance metrics
• Strong English and grammar skills, second language a plus, but not required.
• Sound knowledge of organization's archival processes and systems (hardware, software, applications, operating systems, basic programming languages, etc.), SOPs and training requirements.
• Ability to manage the day-to-day operation of Records Management file rooms including but not limited to document control, security and audit preparedness

Nice To Haves

• second language a plus, but not required.

Responsibilities

• Conduct multiple ongoing clinical trials, of varying size and complexity, involving patients or healthy volunteers/subjects.
• Complete all paperwork required to capture all data as specified by a study protocol, and for ensuring subject safety, understanding, and cooperation during the study process.
• Interact with the research site team and other interdepartmental staff.
• Engage in the entire site operations process, which includes recruitment, enrollment and retention of study participants.
• May act as primary or lead CRC on certain studies, taking the overall responsibility thereof at the site, while maintaining communication and updates with site team, liaising with monitors and other stakeholders.

Benefits

• When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience – and where your contributions truly make a difference.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: No Education Listed