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Manager Clinical Trial Rn Jobs (NOW HIRING)

Ardelyx

Clinical Trial Manager

Waltham, MA · On-site +1

$136K - $160K/yr

Bachelor's degree in Life Sciences, Nursing, or a related field with 5+ years of experience in clinical trial management or related clinical research roles; equivalent experience may be considered

McKesson

OR

Excellent organizational and priority management skills. * Strong computer skills including ... Bachelor's Degree in Nursing or Licensed Registered Nurse * 3+ years of experience as a research ...

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 ...

IQVIA

Clinical Trial Educator

Overland Park, KS

$62.30K - $195.10K/yr

IQVIA is seeking a Registered Nurse to join our team as a Clinical Trial Educator . The ideal candidate will bring strong operating room (OR) experience , along with a passion for educating and ...

AUROBINDO

$125K - $135K/yr

Job OverviewThe Clinical Trial Manager will lead key aspects of assigned clinical trial(s) and demonstrates a good level of knowledge of clinical methodologies, organizational, project management and ...

Tango Therapeutics

Clinical Trial Leader

Boston, MA · Hybrid

Manage trial budgets, change orders, and invoice reconciliation in collaboration with vendor ... Oversee database lock, clinical study report (CSR) development, and study close-out activities.

Collabera

Clinical Trial Manager

Jersey City, NJ

Knowledge and experience in clinical study budgeting including timeline and the application of clinical trial performance metrics. Demonstrated ability to support the development and management of ...

ARTBIO

Senior Clinical Trial Manager

Cambridge, MA · On-site +1

SummaryThe Senior Clinical Trial Manager will lead the day-to-day activities in a clinical trial ... Bachelor's or Master's degree in Life Sciences, Nursing, Pharmacy, or a related field. * 5 to 8 ...

Biogen

Sr. Manager - Clinical Trial Lead

Cambridge, MA · On-site

... clinical trial delivery • Effective CRO management skills and ability to adapt to fit for purpose clinical trial outsourcing strategies and models • Working knowledge of the financial aspects of ...

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

As of May 30, 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.

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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

Ardelyx

Waltham, MA • On-site, Remote

$136K - $160K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 4 days ago

Job description

Ardelyx is a commercial-stage biopharmaceutical company focused on redefining treatment approaches for patients with significant unmet medical needs. By combining scientific innovation with a collaborative, purpose-driven culture, we strive to create meaningful impact for patients.
Team Ardelyx is united by a shared mission and guided by our core values: Passionate, Fearless, Dedicated, and Inclusive.
We foster an inclusive environment where employees are respected, supported, and empowered to make an impact - both within our company and in the lives of patients we serve.

Position Summary (Hybrid Location):

The Clinical Trial Manager (CTM) is responsible for the end-to-end operational oversight of clinical trials, from study planning through close-out and reporting. This role ensures trials are executed ethically, on time, within budget, and in full compliance with applicable regulatory requirements and Good Clinical Practice (GCP), while maintaining the highest standards of patient safety and data integrity.
Responsibilities:
  • Provide operational leadership for one or more clinical studies or programs, overseeing execution from initial study synopsis through final deliverables, including study start-up, enrollment, conduct, database lock, statistical outputs (TLFs), and Clinical Study Report (CSR)
  • Lead study start-up activities in collaboration with CROs and investigational sites, including oversight of clinical document development and site activation activities
  • Manage day-to-day study execution, ensuring adherence to timelines, milestones, budgets and quality standards
  • Contribute to and review study plans, timelines, and operational deliverables; proactively identify risks and implement mitigation strategies to ensure successful study outcomes
  • Prepare, review and/approve study-related documents including but not limited toInformed Consent Forms, CRFs, Monitoring Plans, Laboratory Manuals, Patient Diaries, Clinical Site Procedures Manual and CRF Completion Guidelines)
  • Implement risk management and mitigation strategies, prioritizing tasks and issues to ensure successful program/study objectives
  • Participate in and support user acceptance testing (UAT) for clinical systems, (e.g., EDC IRT), including contribution to system requirements and validation activities
  • Oversee vendor performance and relationships including CROs, central laboratories, and contribute to or lead the systems set-up/management, EDC/IRT, and specialty services (ePRO, ECG, imaging etc.)
  • Ensure compliance with GCP, applicable regulations, SOPs, and study-specific procedures throughout the trial lifecycle
  • Track, analyze and communicate study progress, risks and key metrics to the Study Lead and senior management, including development and maintenance dashboards and trackers
  • Represent Clinical Operations professionally, fostering productive relationships with investigators, CRO partners, vendors and internal cross functional teams
Qualifications:
  • Bachelor's degree in Life Sciences, Nursing, or a related field with 5+ years of experience in clinical trial management or related clinical research roles; equivalent experience may be considered
  • Master's degree and clinical research certification (e.g., CCRA, CCRP) strongly preferred
  • Demonstrated knowledge of current clinical trial processes, GCP, ICH guidelines and regulatory requirements
  • Strong project management skills, including managing of timelines, budgets, and cross-functional resources
  • Excellent written and verbal communication with the ability to lead cross-functional teams and external partners.
  • Proven problem-solving skills and tools, and ability to manage complex operational issues in a fast paced environment
  • Experience with clinical trial systems and tools including EDC, IRT and Veeva Vault platforms,)
  • Ability to travel occasionally to clinical sites, investigator meetings, and professional conferences as required
  • Remote work considered; preference for candidates able to attend the office weekly (Newark or Waltham)
The anticipated annualized base pay range for this full-time position is $136,000-$160,000. Ardelyx utilizes industry data to ensure that our compensation is competitive and aligned with our industry peers. Actual base pay will be determined based on a variety of factors, including years of relevant experience, training, qualifications, and internal equity. The compensation package may also include an annual bonus target and equity awards, subject to eligibility and other requirements.
Ardelyx also offers a robust benefits package to employees, including a 401(k) plan with generous employer match, 12 weeks of paid parental leave, up to 12 weeks of living organ and bone marrow leave, equity incentive plans, health plans (medical, prescription drug, dental, and vision),life insurance and disability, flexible time off, annual Winter Holiday shut down, and at least 11 paid holidays.
Ardelyx is an equal opportunity employer.
Employment Type: Full-Time

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