Clinical Research Coordinator (on-site Daytona Beach, FL)

As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.

This is an office based position in Daytona Beach, FL.

Overall accountability for the operational conduct of assigned studies, working closely with the Project Manager, Principal Investigator and operational staff and ensuring that all studies are conducted in accordance with regulatory and protocol requirements, and standard operating procedures whilst maintaining the safety and integrity of the study .

The Clinical Research Coordinator is the primary site contact for the Project Manager (PM) communicating any potential issues and assists in taking appropriate action in response to these issues, ensuring that client requirements and timelines are always met or exceeded.

Some of the Clinical Research Coordinator's Primary Job Duties include:

• Understands and maintains awareness of sponsor expectations for trial conduct and works to meet or exceed them. Facilitates client visits, and attends client calls with the assistance of the Project Manager and/or site management where appropriate.
• Creates, delivers/facilitates study specific training to all CRU staff.
• Learns and develops clinical skills to perform study tasks and performs procedures if necessary
• Works with the investigators to confirm participant eligibility in studies.
• Oversees volunteer recruitment for assigned studies and partners with the CRU's recruitment team for success.
• Source document/electronic documents creation for assigned studies.
• Ensures all protocol deviations and or unscheduled events are properly documented and communicated.

Qualifications:

• Prefer 3-4 years’ experience in a research environment
• Excellent written and oral communication skills
• Ability to prioritize workloads
• Previous customer experience desirable

Recommended:

• University/college degree desirable (life science, pharmacy or related subject preferred) or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing certification, medical or laboratory technology).
• In lieu of a degree, typically 3 years’ experience in a related field will be considered

Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact. For more information about Fortrea, visit www.fortrea.com .

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Fortrea is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, Fortrea strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. We encourage all to apply.

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