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Manager Clinical Trial Rn Jobs (NOW HIRING)

ICON

Clinical Trial Manager

Blue Bell, PA · On-site +1

Clinical Operations Lead (CTM) The Clinical Operations Lead supports the Clinical Trial Manager/operational team in execution of the trial (s). The position includes direct liaison with CROs and ...

Natera

OR

Current, active licensure as a Registered Nurse, Certified Genetic Counselor, Nurse Practitioner ... A master's degree in a clinical or scientific field is highly preferred. Professional Experience ...

Procter & Gamble

Clinical Trial Manager

Mason, OH · On-site

A P&G Clinical Trial Manager will be responsible for: * Design, implementation, and management of clinical trials, Development of both external and internal networks for the integration of key ...

Ossium Health

Clinical Trial Manager

San Francisco, CA · On-site

$145K - $165K/yr

About the Job We are hiring a Clinical Trial Manager to support the successful execution of our clinical trials and operations. In this role, you'll take ownership of the day-to-day tactical ...

Pramand

Clinical Trial Manager

Bedford, MA

$85 - $110/hr

The Contract Clinical Trial Manager (CTM) will serve as the sponsor-side operational study lead, responsible for day-to-day execution and oversight of clinical trial activities during study start-up ...

Pramand LLC

Clinical Trial Manager

Bedford, MA · On-site

The Contract Clinical Trial Manager (CTM) will serve as the sponsor-side operational study lead, responsible for day-to-day execution and oversight of clinical trial activities during study start-up ...

Arcus Biosciences

Senior Clinical Trial Manager

Summary The Sr. Clinical Trial Manager (CTM) will provide clinical study support to the Clinical Program Manager/Study Management Team Lead (SMTL) for one or more clinical studies, ensuring efficient ...

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How much do manager clinical trial rn jobs pay per hour?

As of Jul 16, 2026, the average hourly pay for manager clinical trial rn in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.

What is the difference between Manager Clinical Trial Rn vs Clinical Research Coordinator?

AspectManager Clinical Trial RnClinical Research Coordinator
CredentialsRegistered Nurse (RN) license, clinical trial experience, possibly certification in researchTypically bachelor's degree in health or related field, research training
Work EnvironmentOversees multiple trials, manages teams, administrative and supervisory dutiesCoordinates daily trial activities, patient interactions, data collection
Employer & Industry UsagePharmaceutical companies, research institutions, hospitalsResearch sites, hospitals, clinics, academic institutions

The Manager Clinical Trial Rn generally has more supervisory responsibilities and clinical expertise, overseeing entire trials and managing staff. In contrast, the Clinical Research Coordinator focuses on daily trial operations and patient interactions. Both roles require research knowledge but differ in scope and seniority.

What cities are hiring for Manager Clinical Trial Rn jobs? Cities with the most Manager Clinical Trial Rn job openings:
What are the most commonly searched types of Clinical Trial Rn jobs? The most popular types of Clinical Trial Rn jobs are:
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Manager Clinical Trial Rn jobs near you
Clinical Trial Manager

Clinical Trial Manager

ICON

Blue Bell, PA • On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

Clinical Operations Lead - Hematology/Von Willebrand Disease
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
Clinical Operations Lead (CTM)
The Clinical Operations Lead supports the Clinical Trial Manager/operational team in execution of the trial (s). The position includes direct liaison with CROs and other ancillary vendors, as appropriate, to manage relevant trial(s) operational tasks. The Lead maintains effective communication with project team through oral and written correspondence, status reports to ensure alignment with study timelines.
  • Assist in the review, development and writing of clinical trial documents and manuals, including but not limited to study manuals, laboratory or biomarker plans, and other supporting documents.
  • Create Master ICF template and review/approve site changes (in consultation with legal, safety when warranted). Update template for new risks and new amendments information.
  • Participate in the feasibility and evaluation of investigative sites; working closing with the Clinical Trial Logistics group.
  • Coordinate and monitor activities at investigational sites; review monitoring trip reports and support the US monitoring organization.
  • Assist in the development and management of study timelines and priorities, including recruitment tools/strategy and patient retentions plan.
  • Plan and organized meetings with team support (eg. investigator/coordinator meetings, DMC, SMC, safety call, etc.).
  • Assist in the development of the IP and co-medication strategy (Quantities, labels, depots, tracking, etc.) working closely with other departments.
  • Participate in data review and discrepancy resolution.
  • Participate in coordinating efforts with internal Pharmacovigilance, and safety group.
  • Monitor study-specific timelines and key deliverables; focus on management of all external vendors (e.g Monitoring, Sample management, IVRS, Laboratory, etc).
  • Participate as a member of the multi-disciplinary trial(s) team.
  • Develop relationships with investigational sites and institutions to enhance conduct of the trial.
  • Acts as preliminary liaison for study sites to convey trial information, answer questions and in accordance with the escalation pathway.
  • Assume responsibility to participate as a member of a working group and perform special projects, as assigned, to improve the efficiency, effective and quality of the functioning of the Development Operations Department.

What you need to have:
  • BS/BA degree or a relevant degree with strong emphasis on science.
  • Minimum of 5 years of clinical trial management experience in the biopharmaceutical industry or other relevant clinical research experience.
  • Candidates must have non-malignant hematology clinical trial management experience/Von Willebrand disease
  • Must have working knowledge of ICH Good Clinical Practices and other relevant regulatory/health authority experience.
  • Ability to effectively manage multiple priorities across several protocols and therapeutic areas simultaneously.
  • Prior experience in assisting the conduct and management of multinational clinical trials is preferred.
  • To qualify, applicants must be legally authorized to work in the United States and should not require, now or in the future, sponsorship for employment visa status

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Are you a current ICON Employee? Please click here to apply

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