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Medical Device Clinical Research Manager Jobs (NOW HIRING)

Wisconsin

Clinical Research Manager

Madison, WI · On-site

$95K/yr

Clinical Research Manager Job Summary: The School Mental Health Collaborative (SMHC), a research ... Experience working with families and youth within a community or medical context focused on mental ...

Impulse Dynamics

Clinical Trial Manager

Marlton, NJ

$95K - $115K/yr

Minimum of 2 years of progressive experience in clinical operations, clinical trial management, or project management within the pharmaceutical, biotechnology, medical device, or contract research ...

Stanford University

Clinical Research Manager

Stanford, CA · On-site

$124K - $153K/yr

The Tass Lab at Stanford University is seeking a Clinical Research Manager to provide leadership ... Knowledge of medical terminology. * Demonstrated managerial experience. CERTIFICATIONS & LICENSES:

Tufts University

Clinical Research Manager

Boston, MA · On-site

$74K - $111K/yr

What You'll Do The Clinical Research Program Manager is the operational lead of the Coordinating Center for a multi-site Lyme disease research program spanning three regional hubs and more than 20 ...

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Medical Device Clinical Research Manager information

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$49K

$107.3K

$189K

How much do medical device clinical research manager jobs pay per year?

As of Sep 2, 2026, the average yearly pay for medical device clinical research manager in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What does a medical device clinical research manager do?

A Medical Device Clinical Research Manager oversees the planning, execution, and management of clinical trials for new medical devices to ensure they meet regulatory and safety standards. They coordinate between research teams, regulatory bodies, and sponsors to ensure studies are conducted according to protocols and timelines. Their responsibilities include developing study protocols, managing budgets, ensuring data integrity, and ensuring compliance with regulatory requirements. This role is critical for bringing safe and effective medical devices to market.

What are the key skills and qualifications needed to thrive as a medical device clinical research manager?

To thrive as a Medical Device Clinical Research Manager, you need a solid background in life sciences or engineering, experience with clinical trial management, and a thorough understanding of regulatory requirements such as FDA and ISO standards. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like ACRP or SOCRA are highly beneficial. Exceptional leadership, problem-solving, and communication skills are crucial for coordinating cross-functional teams and managing complex projects. These skills ensure compliant, efficient, and successful clinical trials that bring safe and effective medical devices to market.

What are some of the common challenges faced by medical device clinical research managers when overseeing clinical trials?

Medical Device Clinical Research Managers often encounter challenges such as ensuring compliance with complex regulatory requirements, managing timelines across multiple sites, and coordinating with diverse stakeholders including investigators, sponsors, and regulatory bodies. They must also address issues related to patient recruitment and data integrity while maintaining clear communication within cross-functional teams. Strong organizational skills and adaptability are essential to navigate these challenges and deliver successful clinical trial outcomes.
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Medical Device Clinical Research Manager jobs near you
Infographic showing various Medical Device Clinical Research Manager job openings in the United States as of August 2026, with employment types broken down into 92% Full Time, and 8% Contract. Highlights an 92% In-person, and 8% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Clinical Research Manager

The US Oncology Network

Cincinnati, OH • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 20 days ago

US Oncology rating

7.1

Company rating: 7.1 out of 10

Based on 109 frontline employees who took The Breakroom Quiz

378th of 898 rated healthcare providers

Job description

Overview

Position: Clinical Research Manager 

Weekly Hours: 40 (full time)

SCOPE:

Responsible for ensuring at the administrative level that all research activities are coordinated with affected departments within the practice. Coaches and develops staff. Collaborates in the development of research accountability standards and identifies areas for improvement. Ensures site research quality by practicing in compliance with US Oncology Research, Inc. (USOR) Standard Operating Procedures (SOP), principles of Good Clinical Practice (GCP) and applicable federal, state, and local regulations. Supports and adheres to the US Oncology Compliance Program, to include Code of Ethics and Business Standards.

Why choose OHC?  

You take care of our patients, so we take care of you. OHC’s benefits include:

  • 3 Health Insurance Plans to choose from 
  • 2 Dental and 2 Vision insurance plans 
  • A company 401K plan
  • Profit sharing plan for clinical employees
  • Competitive salaries
  • Company paid short term / long term disability / life insurance 
  • Paid Holidays 
  • A generous PTO plan 
  • Tuition Reimbursement 
  • Professional Development Program
  • Nationwide Discounts at your favorite hotels, resorts and retailers just for being an OHC employee
  • Wellness Program
  • Periodic merit raises 
  • Opportunities for advancement

About the company:
OHC has served as the region’s premier provider of treatments for cancer and blood disorders, offering a wide range of services and state-of-the-art treatments and technologies, as well as being nationally recognized for cutting edge clinical research breakthroughs in Southwest Ohio area for over 40 years. Serving patients close to home through our Cancer Centers of Excellence in Fairfield, West side of Cincinnati, Blue Ash, Kenwood and Eastgate in Ohio. OHC puts patients first by delivering compassionate and convenient care, tailored to meet a patient’s medical and personal needs.


Responsibilities

Key Responsibilities

  • Supervises clinical research staff members in accordance with USOR SOP and ICH GCP guidelines. Responsible for ensuring at the administrative level that all research activities are coordinated with affected departments within the practice.

  • Coaches and develops staff. Participates in the recruitment, interviewing, hiring, assessing performance, recommending salary changes, and progressive discipline. Enforces adherence to company policies.

  • Collaborates in the development of research accountability standards, metrics, and reports and identifies areas for improvement. Collaborates with site research leader (SRL), upper management, and staff in the implementation of action plans designed to improve practice research operations and quality assurance functions.

  • Collaborates with the SRL, physicians of the practice, and other research management in the process of study selection for the research program.

  • Collaborates with SRL and upper management on the development of research budgets, financial objectives, and accrual targets.

  • May promote or market research program to the practice, community, and referring physicians.

  • May coordinate research activities with other (non-USOR) bases or sponsors.


Qualifications

Minimum Job Qualifications (Knowledge, Skills, & Abilities):

Education/Training –

  • Associates degree in a clinical or scientific related discipline required

  • Graduate of an accredited nursing program preferred

Business Experience -

  • Minimum 5 years clinical nursing experience or scientific related discipline required, preferably in oncology

  • Supervisory experience preferred, experience in clinical research preferred

  • If required in state of practice, current licensure as a registered (RN)

  • Current BCLS or ACLS certification for nurses

  • SoCRA or ARCP certification preferred

Specialized Knowledge/Skills -

  • Excellent communication skills

  • Strong ability to multitask, strong interpersonal skills

  • Must be able to work in a fast-paced, constantly changing environment

  • Knowledge and proficiency in all basic computer programs, Windows, Excel, etc.

  • Special knowledge of GCP and ICH guidelines preferred

  • Knowledge of medical terminology, nursing assessment, clinical medicine, diagnostic tests, radiology, pathology, pharmacology, hematology, oncology as it relates to clinical trials

Qualifications:

Minimum Job Qualifications (Knowledge, Skills, & Abilities):

Education/Training –

  • Associates degree in a clinical or scientific related discipline required

  • Graduate of an accredited nursing program preferred

Business Experience -

  • Minimum 5 years clinical nursing experience or scientific related discipline required, preferably in oncology

  • Supervisory experience preferred, experience in clinical research preferred

  • If required in state of practice, current licensure as a registered (RN)

  • Current BCLS or ACLS certification for nurses

  • SoCRA or ARCP certification preferred

Specialized Knowledge/Skills -

  • Excellent communication skills

  • Strong ability to multitask, strong interpersonal skills

  • Must be able to work in a fast-paced, constantly changing environment

  • Knowledge and proficiency in all basic computer programs, Windows, Excel, etc.

  • Special knowledge of GCP and ICH guidelines preferred

  • Knowledge of medical terminology, nursing assessment, clinical medicine, diagnostic tests, radiology, pathology, pharmacology, hematology, oncology as it relates to clinical trials

Education:UNAVAILABLEEmployment Type: FULL_TIME

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