ZipRecruiter

Log In

1

Epic Clinical Program Manager Jobs (NOW HIRING)

RSM

Supervisor - Epic Clinical Analyst

Charlotte, NC · On-site

We are currently seeking anEpic Clinical Subject Manager & Project Manager to join our Healthcare ... programs. The Supervisor willleveragestrong Epic clinicalexpertise, healthcare operational ...

RSM

Supervisor - Epic Clinical Analyst

Denver, CO · On-site

We are currently seeking anEpic Clinical Subject Manager & Project Manager to join our Healthcare ... programs. The Supervisor willleveragestrong Epic clinicalexpertise, healthcare operational ...

First Place for Youth

Clinical Program Manager

Oakland, CA · On-site

$109K - $116K/yr

The Clinical Manager reports to the Director of Programs. This position requires a clinical professional whose passion for First Place's vision is matched with energetic leadership, sound judgment in ...

Essc

Clinical Program Manager

Bakersfield, CA · On-site

$70K/yr

Under supervision by a Board Certified Behavior Analyst (Assoc. Clinical Supervisor, Clinical Supervisor, or Regional Clinical Director), provides program management and executes changes in program.

New

Essc

Clinical Program Manager

Covina, CA · On-site

$70K/yr

Under supervision by a Board Certified Behavior Analyst (Assoc. Clinical Supervisor, Clinical Supervisor, or Regional Clinical Director), provides program management and executes changes in program.

VOALA

$104K - $109K/yr

JOB SUMMARY The Clinical Program Manger I supervises all efforts to fulfill the goals and objectives of the Program, designing plans and operations according to contract and budget guidelines. This ...

Osv_bioventus

Clinical Program Manager

Durham, NC · On-site

Main Purpose of the Role The CPM Clinical Program Manager (CPM) will plan, initiate, and execute regional and global clinical studies and projects in orthopedic devices and biologics, ensuring ...

VOALA

Clinical Program Manager

California, MO · On-site

$104K - $109K/yr

JOB SUMMARY The Clinical Program Manger I supervises all efforts to fulfill the goals and objectives of the Program, designing plans and operations according to contract and budget guidelines. This ...

Osv_bioventus

Clinical Program Manager

Durham, NC

Main Purpose of the Role The CPM Clinical Program Manager (CPM) will plan, initiate, and execute regional and global clinical studies and projects in orthopedic devices and biologics, ensuring ...

Bioventus

Clinical Program Manager

Durham, NC · On-site

Main Purpose of the Role The CPM Clinical Program Manager (CPM) will plan, initiate, and execute regional and global clinical studies and projects in orthopedic devices and biologics, ensuring ...

previous page

Showing results 41-60

All JobsHealthcare JobsHospital JobsEpic Clinical Program Manager Jobs

Epic Clinical Program Manager information

See salary details

$44.5K

$92.6K

$149.5K

How much do epic clinical program manager jobs pay per year?

As of Sep 13, 2026, the average yearly pay for epic clinical program manager in the United States is $92,603.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,500.00 and $105,000.00 per year, depending on experience, location, and employer.

What are popular job titles related to Epic Clinical Program Manager jobs?

For Epic Clinical Program Manager jobs, the most frequently searched job titles are:

Infographic showing various Epic Clinical Program Manager job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 16% Part Time, and 4% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $92,603 per year, or $44.5 per hour.

Clinical Program Manager

Redwood City, CA • Hybrid

Revolution Medicines
See more jobs at Revolution Medicinesexternal

Full-time

Re-posted 6 days ago

Job description

The Opportunity: 

This is a unique opportunity for a Clinical Operations Professional. As a Clinical Program Manager (CPM), you will be responsible for acting as a central contact for the Clinical Study Team(s) and assist with the execution and management of Revolution Medicines (RevMed) clinical trials.

  • Adhere to Clinical Standard Operating Procedures (SOP), Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) Guideline.

  • Be a team leader, providing guidance and oversight for the successful management of all aspects of clinical trials within timelines and designated program budgets.

  • Partner with cross-functional teams to manage, adjust, and revise project timelines and budgets as needed

  • Analyze data health metrics to be shared with stakeholders.

  • Actively partner with cross-functional teams and vendors to drive the query resolution and data listings review process to meet objectives in a timely and efficient process.

  • Conduct risk management, contingency, and scenario planning.

  • Supervise, communicate project status/issues, and problem solve to ensure project team goals are met .

  • Participate in the development of all study-related documentation, including study protocols.

  • Actively contributes in the selection and management of contract research organizations (CROs) and/or vendors, including development of requests for proposals (RFPs).

  • Use all available tools to track, oversee, and communicate on program status to all key stakeholders.

  • Participate in other Clinical Operations activities as appropriate.

  • Leads a larger, more complex trial with some oversight from senior members of Clinical Operations.

  • With minimal support, lead cross-functional Clinical Study Execution Team (CSETs).

  • Participate in and contribute to SOP development, implementation, and training.

  • Support junior team members through mentorship.

Required Skills, Experience and Education:

  • RN or Bachelor's or Masters degree in biological sciences or health-related field required.

  • 8+ years direct Clinical Operations experience in the pharmaceutical or biotech industry, preferably in Clinical Operations or Clinical Research-related experience. Relevant indirect experiences may also meet the requirement.

  • Minimum of 4 years of cross-functional study management or related leadership experience in life sciences, including multiple years' experience managing project teams.

  • Strong working knowledge of FDA Regulations, ICH Guidelines, and GCP.

  • Proven ability to successfully start-up, manage, and close-out clinical trials, including authoring clinical study and regulatory documentation and SOPs.

  • Experience in selection of CROs/vendors and management of external resources.

  • Thrives in a collaborative team setting that demonstrates flexibility required to maintain a fast pace and is driven by a desire to deploy innovative approaches and technologies in a high-energy environment.

  • Be solution-oriented by anticipating obstacles and difficulties, and proactively providing risk assessment and mitigation strategies to achieve project goals.

  • Excellent written/verbal communication and interpersonal skills.

  • High sense of priority and commitment to excellence in the successful execution of deliverables.

  • Ability to analyze operational data, contribute with a mind on quality, timeliness and fiscal responsibility, make and drive decisions, multi-task, prioritize tasks, anticipate challenges, and execute on goals as a member of an interdisciplinary team.

  • Demonstrate proficiency in Microsoft Office Suite (Outlook, MS Word, Excel, PowerPoint); MS Project and/or Smartsheet a plus.

  • Travel may be required (~25%).

Preferred Skills:

  • Familiarity working with vendor systems/portals (e.g., eTMF, EDC, IRT, CTMS).

  • Oncology experience, early and/or late stage, strongly preferred.

  • Knowledge and/or familiarity with Ex-US region(s) clinical trial operations.

  • Some experience mentoring jr staff.

#LI-DN1 #LI-Hybrid

Apply