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.

Clinical Operations Manager

Onsite - Madison, Wisconsin

Are you a strong leader motivated by making a difference and impacting change? If so, this is the right opportunity for you to learn more about today! As a Clinical Operations Manager you are responsible first and foremost for the management, administration, organization and conduct of the Study Operations department. This role needs someone who is strong in leadership, passionate about training along with coaching and someone confident in mentoring of clinical operations staff.

What to Expect

(job duties include but not limited to below)

• Directly or indirectly supervise clinical operations technical and professional staff.

• Ensure that all work is carried out in strict adherence with relevant protocols, SOP's, and in compliance with ICH/GCP guidelines. Ensure that Operations staff is trained and compliant with SOP's and Skills checks. Ensure that all training files are up to date and complete in accordance with SOPs and ICH/GCP.

• Ensure that the scientific and medical standards provided are met.

• Assist client services with developing client proposals and attend client meetings as needed.

• Assist client services with client visits and interactions as appropriate.

• Initiates collaborative relationships with external institutions when protocol required.

• Initiates procurement of external resources, consultants, or equipment when protocol required.

• Assist with the development of Operation's department budget.

• Responsible for all aspects of project related matters in agreement with client and supervisory personnel.

• Make recommendations for timing, logistics, and feasibility for proposed studies.

• Meet the overall schedule agreement with the client.

• Ensure that appropriate cost monitoring systems are in place and that accurate project accountability is maintained.

• Sets standards, policies, and guidelines for the efficient management of clinical operations.

• And perform other duties and or tasks as assigned.

Education / Qualifications

• BS in Science or Medical Field

• English written and oral communication required

Experience

• 6-8 years clinical research experience; preferred

• Minimum of 5 years supervisory experience or 4-5 years of progressive and proven leadership responsibilities in clinical research coordination/management

• Six Sigma Green Belt is preferred

• Additional experience may be substituted for education requirements

Benefits:

• Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers)

• 401(K)

• Employee recognition awards

• Multiple ERG's (employee resource groups)

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.

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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