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Manager Clinical Trial Rn Jobs (NOW HIRING)

VENESCO, LLC

Clinical Trial Manager

Fort Detrick, MD · On-site

$125K - $143K/yr

Description Clinical Trial Manager Venesco LLC is seeking Clinical Trial Managers to provide leadership and operational oversight for FDA-regulated clinical studies, ensuring studies are executed in ...

Brave

Clinical Trial Management Associate

San Francisco, CA · On-site

$100 - $135/hr

... Clinical Trial Manager (CTM), Senior CTM, and Associate Director, Clinical Operations. The CTMA ... Required experience & skills: * BS or BA in a relevant scientific discipline or RN (2‑ or ...

New

Kardigan

Clinical Trial Manager

Princeton, NJ · On-site

As a Clinical Trial Manager (CTM), you will be part of the Clinical Operations team reporting to the asset's Clinical Trial or Clinical Program Lead. This position will be responsible for the ...

ICON

Senior Manager Clinical Trial Lead

Blue Bell, PA · On-site

Key contributor to the development of annual trial/project objectives and communicating to relevant line management and Clinical Operations Team. * Drives and leads the successful execution ...

McLaren

Clinical Research Registered Nurse

Detroit, MI · On-site

... or registered to a clinical trial. The CRN provides specialized nursing care that ensures ... Responsible for managing patient standard of care needs as well as participant and protocol needs ...

Kymera Therapeutics

Clinical Trial Manager

Watertown, MA · On-site

$115K - $200K/yr

Responsible for management of vendors to support clinical trial execution * Plan, execute, and lead study-specific meetings (e.g., internal core team meetings, investigator meetings, etc), as needed

Lumicell

Senior Clinical Trial Manager

Waltham, MA · On-site

Advanced degree such as MPH, MS, RN, PharmD, or equivalent. * Combination product experience or medical device experience. * Oncology experience. * Experience managing registries and post-market ...

Posted today

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

As of Aug 7, 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.

How do I become a manager clinical trial RN?

To become a manager clinical trial RN, you typically need a registered nurse (RN) license, experience in clinical research or patient care, and often a bachelor's degree in nursing or a related field. Gaining experience in clinical trial coordination, research protocols, and obtaining certifications such as Certified Clinical Research Professional (CCRP) can enhance qualifications for leadership roles.
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:
What states have the most Manager Clinical Trial Rn jobs? States with the most job openings for Manager Clinical Trial Rn jobs include:
Manager Clinical Trial Rn jobs near you

Clinical Trial Manager

SAGIMET BIOSCIENCES INC.

San Mateo, CA

$90 - $100/hr

Full-time

Posted 23 days ago

Job description

Description

The Clinical Trial Manager manages and leads the day-to-day clinical trial activities related to the development and execution of cross-functional and third-party vendor activities and deliverables. Additional responsibilities include Independent oversight of outsourced clinical studies, protocol review for operational feasibility and consistency, CRO/vendor feasibility, request for proposal and bid defense process, country/site feasibility, tracking site selection, activation, and patient recruitment. The Clinical Trial Manager will also focus on the management of project timelines, relevant study plans (e.g. monitoring, study operations, quality, communications, etc.), EDC and IXRS set up and development and/or review of clinical data management conduct (e.g. eCRFs, CRF guidelines). 


 Essential Responsibilities:

 Clinical operations leader and main point of contact with counterpart at outside vendor, CRO and/or trial sites; daily review and identification of potential issues or problems and communicates/escalates to project team. 

Assist in the critical development and review of key study documents (e.g. Protocols, ICF, study plans eCRF, etc.). 

Develop, maintain and promote effective and collaborative working relationships with and among internal team members and external vendors and 3rd party personnel. 

Participate in Clinical Operations meetings as assigned.  

Lead reviews of key data to identify trends, discrepancies, errors etc. to ensure ongoing quality of conduct in accordance with the protocol and vendor contracts, including on-going review of emerging data for tables, listings, and figures. 

Work with junior CTM for oversight of in-house review of site monitoring reports and tracking to ensure appropriate monitoring of trial conduct and satisfactory resolution of outstanding issues. 

Work with junior CTM for oversight of Trial Master Files (TMF) oversight plan and laisses with CRO for annual quality check; ensuring tracking of ICH-GCP and/or FDA CRF21 essential study documents. 

Track patient and recruitment status using applicable spreadsheets and web portal tools. 

Assist in yearly IND updates including IBs and DSUR. 

Requirements

A minimum of a Bachelor's degree or equivalent is required, preferably in Life Sciences (e.g. Biology, Chemistry, Biochemistry, Nursing, Pharmacy) 

A minimum of ten years clinical operations experience 

A minimum of three years of experience leading clinical trials from start-up to database lock 

Experience with all three parts of leading a global Phase 2 and/or Phase 3 clinical trial: start up, treatment phase and database lock. 

Experience in start up and oversight of central lab, including depth specification review. 

Knowledge of sample collect and analysis process at the study level and may perform reconciliation and/or tracking of sample manifests. 

Experience with data privacy and GDPR guidelines.  

Experience with the independent management and oversight of CROs/vendors required. 

Experience with double blind/placebo controlled studies required. 

Experience within a small biotech organization and flexibility to pivot quickly and think outside the box. 

Excellent attention to detail, accuracy in work and possesses strong analytical skills. 

Must think critically and creatively and be able to work independently to determine appropriate actions to resolve complex problems. 

Comprehensive knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials 

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