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Clinical Affairs Manager Jobs (NOW HIRING)

The Clinical Affairs Manager, Interventional Urology develops, manages, and delivers professional education to surgeons, OR staff, and sales representatives to achieve exceptional clinical outcomes ...

The Clinical Affairs Manager, Interventional Urology develops, manages, and delivers professional education to surgeons, OR staff, and sales representatives to achieve exceptional clinical outcomes ...

About the Job As the Clinical Affairs Manager (Part-Time) , you will lead clinical affairs and drive adoption of our breakthrough fetal monitoring technology. This role will be critical in bridging ...

Develop and manage the clinical affairs budget, ensuring cost‑effective execution of clinical trials while meeting timelines and quality standards. * Collaboration & Leadership : Partner with ...

Support Clinical Affairs Department in ensuring timely and accurate clinician timesheets ... requests, and manager request changes. * Ensure follow-up for approvals of allocation changes ...

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Clinical Affairs Manager information

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$63.5K

$106.2K

$164.5K

How much do clinical affairs manager jobs pay per year?

As of Jul 13, 2026, the average yearly pay for clinical affairs manager in the United States is $106,193.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,500.00 and $135,000.00 per year, depending on experience, location, and employer.

What is the difference between Clinical Affairs Manager vs Clinical Research Associate?

AspectClinical Affairs ManagerClinical Research Associate
Required credentialsBachelor's or higher in life sciences, often with certifications in clinical researchBachelor's in life sciences, with certifications like CCRP or RAC often preferred
Work environmentOversees clinical trials, manages teams, liaises with regulatory bodiesMonitors clinical trial sites, collects data, ensures protocol compliance
Employer and industry usagePharmaceutical, biotech, medical device companies, CROsResearch sites, CROs, pharmaceutical companies

The Clinical Affairs Manager focuses on overseeing clinical trial operations, regulatory compliance, and team management, while the Clinical Research Associate primarily monitors trial sites and ensures protocol adherence. Both roles require similar educational backgrounds and certifications but differ in scope and responsibilities within the clinical research process.

What are the key skills and qualifications needed to thrive as a Clinical Affairs Manager, and why are they important?

To thrive as a Clinical Affairs Manager, you need a strong background in clinical research, regulatory compliance, and project management, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) guidelines, and regulatory submission processes such as FDA or EMA requirements is crucial. Exceptional leadership, problem-solving, and communication skills help you coordinate teams and manage complex projects effectively. These competencies are vital for ensuring regulatory adherence, advancing clinical studies, and supporting successful product development in healthcare organizations.

What does a Clinical Affairs Manager do?

A Clinical Affairs Manager oversees the planning, execution, and management of clinical trials for medical devices, pharmaceuticals, or biotechnology products. They ensure studies comply with regulatory requirements, manage budgets and timelines, and coordinate with cross-functional teams such as regulatory, medical, and research staff. Their role is crucial in generating clinical evidence necessary for product approvals and post-market surveillance. Effective communication and strong organizational skills are essential for success in this position.

How does a Clinical Affairs Manager typically collaborate with cross-functional teams during a clinical trial?

A Clinical Affairs Manager works closely with cross-functional teams such as regulatory affairs, research and development, quality assurance, and marketing throughout the lifecycle of a clinical trial. They coordinate with these teams to ensure that clinical studies are designed, conducted, and reported in compliance with regulatory requirements and company goals. Regular meetings, clear communication, and effective project management are essential to align timelines, manage resources, and address any challenges that arise. This collaborative environment helps ensure that clinical evidence supports product claims and market approval.
More about Clinical Affairs Manager jobs
What cities are hiring for Clinical Affairs Manager jobs? Cities with the most Clinical Affairs Manager job openings:
What are the most commonly searched types of Clinical Affairs jobs? The most popular types of Clinical Affairs jobs are:
What states have the most Clinical Affairs Manager jobs? States with the most job openings for Clinical Affairs Manager jobs include:
Infographic showing various Clinical Affairs Manager job openings in the United States as of July 2026, with employment types broken down into 83% Full Time, 4% Part Time, and 13% Contract. Highlights an 87% In-person, and 13% Remote job distribution, with an average salary of $106,193 per year, or $51.1 per hour.
Clinical Affairs Manager

Clinical Affairs Manager

Teleflex

Orlando, FL

Other

Medical, Dental, Vision, Retirement, PTO

Posted 5 days ago


Teleflex rating

8.2

Company rating: 8.2 out of 10

Based on 26 frontline employees who took The Breakroom Quiz


Job description

Expected Travel: More than 50%

Requisition ID: 14076

About Teleflex Incorporated

As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people's lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare. 
Teleflex is the home of Arrow, Barrigel, Deknatel, LMA, Pilling, QuikClot, Rusch, UroLift and Weck - trusted brands united by a common sense of purpose.
At Teleflex, we are empowering the future of healthcare.  For more information, please visit teleflex.com.

Interventional Urology - The Interventional Urology business unit of Teleflex is dedicated to developing innovative, minimally invasive and clinically effective devices that address unmet needs in the field of urology. Our flagship product, the UroLift System, is the #1 minimally invasive procedure in the U.S. for treating an enlarged prostate, also called Benign Prostatic Hyperplasia, or BPH.* It is a proven approach that does not require heating, cutting, or destruction of prostate tissue.1 Join a dynamic, growing team that offers healthcare providers an array of medical technology solutions that make a difference in patients' lives.

*U.S. 2022 estimates based on US Market Model 2022-24 (5-17-22 FINAL), which is in part based on data provided by Symphony Health PatientSource 2018-21, as is and with no representations/warranties, including accuracy or completeness.
1. Roehrborn, Can J Urol 2017

Position Summary

The Clinical Affairs Manager partners with the commercial organization to support the safe and effective of the Teleflex MCS product portfolio.  The CAM is responsible for education/scientific presentation development and delivery, peer to peer exchange, comprehensive needs assessments and regional training plan. This role plays a pivotal position in supporting customer experience and patient centric care.

The Clinical Affairs Manager, Interventional Urology develops, manages, and delivers professional education to surgeons, OR staff, and sales representatives to achieve exceptional clinical outcomes for patients. As an integral member of the Clinical Affairs team, this position manages, coordinates, and facilitates peer-to-peer training, residency programs, new product development training, new hire training, case coverage, and other training activities. This position requires OR-based training experience, strong people skills, and the ability to perform at high-levels independently in a fast paced, dynamic environment.

Principal Responsibilities
  • Customer Experience - Representing Teleflex in a customer facing position is a tremendous responsibility and opportunity.  All CMA colleagues are expected to perform with the highest levels of professionalism, service and ethics in order to strengthen the Teleflex brand and relationship with our customers.
  • Continuous Improvement - Demonstrates initiative and critical thinking to identify, prioritize process and performance gaps.  Develops solutions to deliver improving results. Exemplifies continuous improvement thought processes and focus. 
  • Culture and Values - Exemplifies Teleflex values and ensures a fair, open and productive climate that is engaging, ethical and legally compliant.  Strives to work effectively across boundaries in a complex matrix environment.
  • Develop/Update content for training courses including Peer to Peer events and HCP & field training.
  • Manage a positive learning experience that builds champions through screening, vetting, and conducting peer-to-peer consults and programs for HCPs and faculty.
  • Manage peer-to-peer events (dinners, case days, office management), including hosting peer-to-peer meals and managing flow for the program.
  • Provide advanced training and education for physicians to advance procedural independence.
  • Manage and process invoices for all faculty events, including peer-to-peer, proctorships, teleconsults, and webinars.
  • Develop and manage Residency Programs in assigned areas.
  • Develop and manage training programs, including online programs, simulators, and live presentations for the commercial team and faculty.
  • Partner with Field Trainers to manage and facilitate hands-on clinical training at New Hire Training.
  • Manage and follow-up with new hires to ensure attainment of qualifications and achievement of training requirements and ensure job performance is in accordance with training SOPs.
  • Develop and manage supplemental physician case trainings, including New Physician, Advanced Anatomy/Obstructed Median Lobes, and Advanced Techniques.
  • Partner with the commercial team to manage and support case coverage.
  • Partner with R&D and Marketing on managing and developing new product launches, market acceptance, case data follow-up reports, videos, video consents, and any other Market Acceptance Testing (MAT) data.
  • Participate in cadaver labs, looking at design changes and evaluating future product enhancements.

Other

  • Partner with Marketing and Clinical Affairs to develop webinar content and conduct webinars with faculty and team members.
  • Partner with cross-functional teams to provide customers a company touch point.
  • Manage and facilitate clinical breakout sessions as needed at meetings.
  • Present Professional Education and Clinical information.
  • Perform other duties as assigned.
  • Contribute to our culture of being collaborative, respectful, transparent, ethical, efficient, high-achieving, and fun!
Education / Experience Requirements
  • Bachelor's degree is required, preferably in clinical, biology, health sciences, or engineering.
  • Minimum of 8 years of professional training or OR-based sales experience.
  • Medical device experience is a plus. Urology experience preferred.
  • Demonstrated clinical mastery related to surgical devices.
  • HCP Engagement experience is a plus.
  • Proficient in Microsoft Word, Excel, and PowerPoint required; Prezzi, Video editing, Articulate, SalesForce experience preferred.
Specialized Skills / Other Requirements
  • Must possess excellent verbal and written communication skills.
  • Detail-oriented with strong organizational skills.
  • Strong work ethic and ability to operate independently.
  • Strong people skills and experience training surgeons in an OR setting.
  • Ability to multitask and meet deadlines.
  • Ability to work in a fast-paced, changing environment.
  • Ability to collaborate with a broad range of personalities.
  • Ability to quickly resolve challenges.
  • Must be able to establish and maintain credentials (via RepTrax, Vendormate, etc.) to have the ability to enter and work, as required, in hospitals and other medical facilities, as an essential function of the job. Depending on customer/site requirements, vendor credentials may require the employee to obtain the COVID-19 as required by facility requirements.
  • Valid driver's license issued by the state in which the individual resides; good driving record.
  • Responsible for performing all duties in compliance with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements with which Teleflex complies.

TRAVEL REQUIRED: 60% (Domestic and International; overnight required)

The pay range for this position at commencement of employment is expected to be between$109,800-$164,700; however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience.  The total compensation package for this position will also include benefits such as medical, prescription drug, dental and vision insurance, flexible spending accounts, participation in 401(k) savings plan, and various paid time off benefits, such as PTO, short- and long-term disability and parental leave, dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment.

If hired, employee will be in an "at-will position" and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.

#LI-LP1

At Teleflex, we follow a comprehensive hiring process. We do not accept unsolicited resumes from agency recruiters or 3rd party firms. We do not make unsolicited job offers. We do not ask for money or require equipment purchase up-front.

Teleflex Incorporated is an equal opportunity employer. Applicants will be considered without regard to age, race, religion, color, national origin, ancestry, sexual orientation, disability, nationality, sex, or veteran status. If you require accommodation to apply for a position, please contact us at: 877-880-8588 or Talent@Teleflex.com.

Teleflex, the Teleflex logo, Arrow, Barrigel, Deknatel, LMA, Pilling, QuikClot, Rusch, UroLift and Weck are trademarks or registered trademarks of Teleflex Incorporated or its affiliates, in the U.S. and/or other countries. 
2026 Teleflex Incorporated. All rights reserved.

 


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