Clinical Research Coordinator

Work Schedule

Environmental Conditions

Job Description

Join us as Clinical Research Coordinator - And manage the day-to-day operations of our clinical trials.

What Youll 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 studyprocess. 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.

Education and Experience:
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.

Knowledge Skills and Abilities:
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 organizations 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

Working Conditions and Environment:
Work is performed in an office environment with exposure to electrical office equipment.
Frequently drives to site locations with possible travel both domestic and international for sponsor or industry related meetings.

Physical Requirements:
Frequently stationary for 6-8 hours per day and/or frequent daily movement depending on study

activities.
Repetitive hand movement of both hands with the ability to make fast simple repeated movements of the fingers hands and wrists.
Moderate mobility required.
Occasional crouching stooping bending and twisting of upper body and neck.
Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-40 lbs.
Ability to access and use a variety of computer software developed both in-house and off-the-shelf. Able to communicate information and ideas so others will understand; with the ability to listen to and understand information and ideas presented through spoken words and sentences.
Frequently interacting with others relates sensitive information to diverse groups both internally & externally.
Ability to apply basic principles to solve conceptual issues.
Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to perform under stress. Ability to multi-task.
Regular and consistent attendance.

Why Join Us
When you join Thermo Fisher Scientific you become part of a global team that values passion innovation and a commitment to scientific excellence. Youll work in an environment where collaboration and development are part of the everyday experience and where your contributions truly make a difference.

Apply today to help us deliver tomorrows breakthrough.