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.

I. Job Summary:
Responsible for ensuring that all practical aspects of clinical studies are conducted to the highest possible quality and in accordance with the protocol, SOPs and ICH/GCP standards. Provides leadership, training, coaching and mentoring for study staff.

• Directly supervises staff which may consist of RNs, LVN/LPNs, and Research Technicians.
• Current knowledge of ICH/GCP standards.
• Demonstrate ability to lead by example and to encourage team members to seek solutions.
• Ensure that the safety, welfare and dignity of research subjects are not compromised.
• Ensure the quality of service provided by team members meets the requirements of both internal and external clients.
• Instill in all team members responsible to him/her the Company's commitment to quality and meeting the client's requirement without error, on time, every time.
• Ensure that appropriate training programs are in place so that all personnel under his/her supervision are adequately and properly trained for their job requirements.
• Ensure that all training files are up to date and complete in accordance with SOPs and ICH/GCP.
• Assist with planning of study set up, as needed.
• Manage his/her area so as to meet the budgeted standard of performance.
• Performs supervisory duties including but not limited to interviewing, hiring, training, intervention, discipline, and discharge of operations staff.
• Ensures that up to date manuals of SOPs and Policy and Procedures are available to all personnel in his/her work area.
• Updates or creates SOPs/P&Ps germane to their area of expertise

Qualifications:

• BS in science or medical field or LPN, LVN or AD degree
• 3 years related experience including 1-2 years of research experience with a BS degree.
• 5-7 years of related experience including 1-2 years of research experience with a LPN, LVN or AD degree
• 1 year of supervisory experience.
• Additional experience may be substituted for education

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 .

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.

For more information about how we collect and store your personal data, please see our.