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Volunteer Clinical Studies Jobs (NOW HIRING)

Clinical Trial Manager

Minneapolis, MN · On-site

$108.19K - $162.29K/yr

This position is member of the clinical study team supporting research activities. It is ... Participate in team-building activities, volunteer opportunities, and company-sponsored events.

Manager, Clinical Research

Paramus, NJ · On-site

$110K - $135K/yr

Maintain oversight of assigned study vendors (e.g. central labs). * Perform assigned activities in ... Medical, Dental & Vision Insurance, Basic and Voluntary Life and AD&D Insurance, Short- and ...

Clinical Trial Manager

Minneapolis, MN · On-site

$108.19K - $162.29K/yr

This position is member of the clinical study team supporting research activities. It is ... Participate in team-building activities, volunteer opportunities, and company-sponsored events.

Manager, Clinical Research

Paramus, NJ · On-site

$110K - $135K/yr

Maintain oversight of assigned study vendors (e.g. central labs). * Perform assigned activities in ... Medical, Dental & Vision Insurance, Basic and Voluntary Life and AD&D Insurance, Short- and ...

Lead - Clinical Study Management

Austin, TX · On-site

$123.50K - $184.78K/yr

This is your opportunity to lead complex, global studies that make a real difference to patients ... Volunteer time and a variety of wellness offerings such as EAP. Smith+Nephew provides equal ...

... volunteerism. We give our best effort to our work, and we put people first. We're looking for ... This role requires in-depth understanding of the clinical study design, data standards, study ...

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Showing results 1-20

Volunteer Clinical Studies information

See salary details

$22K

$125.3K

$206K

How much do volunteer clinical studies jobs pay per year?

As of May 28, 2026, the average yearly pay for volunteer clinical studies in the United States is $125,290.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,000.00 and $157,000.00 per year, depending on experience, location, and employer.

What is the difference between Volunteer Clinical Studies vs Clinical Research Coordinators?

AspectVolunteer Clinical StudiesClinical Research Coordinators
Required CredentialsMinimal; often no formal certification neededTypically requires a degree in health sciences and certification
Work EnvironmentParticipate in clinical trials, often in research facilities or hospitalsManage and oversee clinical trials, working in research settings or hospitals
Employer & Industry UsageResearch institutions, hospitals, pharmaceutical companiesResearch institutions, hospitals, pharmaceutical companies
Search & Comparison IntentUnderstanding volunteer roles in clinical trialsLearning about clinical trial management careers

Volunteer Clinical Studies involve participants who assist in clinical trials without formal healthcare credentials, mainly focusing on participation. Clinical Research Coordinators are professionals responsible for managing and coordinating clinical trials, requiring relevant education and certifications. Both roles are integral to clinical research but differ in responsibilities and qualifications.

More about Volunteer Clinical Studies jobs
What cities are hiring for Volunteer Clinical Studies jobs? Cities with the most Volunteer Clinical Studies job openings:
What are the most commonly searched types of Clinical Studies jobs? The most popular types of Clinical Studies jobs are:
What states have the most Volunteer Clinical Studies jobs? States with the most job openings for Volunteer Clinical Studies jobs include:
Infographic showing various Volunteer Clinical Studies job openings in the United States as of May 2026, with employment types broken down into 3% As Needed, 79% Full Time, and 18% Part Time. Highlights an 75% Physical, 5% Hybrid, and 20% Remote job distribution, with an average salary of $125,290 per year, or $60.2 per hour.
Clinical Trial Manager

Clinical Trial Manager

Comfort Medical

Minneapolis, MN • On-site

$108.19K - $162.29K/yr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 29 days ago


Job description

 

This position is member of the clinical study team supporting research activities. It is responsible for driving and managing clinical studies to support marketing and regulatory needs. This position will be a primary communication liaison between organization and customers participating as investigational sites on clinical studies. This position will also oversee project management and will delegate tasks to the clinical team members according to project plan. This position will comply with regulations and ensure clinical activities comply with organizational SOPs and global regulatory requirements.

Major Areas of Accountability

  • Manage and oversee clinical studies from concept to study close out
  • Contribute to development of clinical strategy; including Clinical Evidence Plans (CEP) and Clinical Development Plans (CDP)
  • Develop clinical investigation plans for regulatory and marketing purposes
  • Develop and oversee project plans and budgets
  • Conduct initiation and site qualification visits
  • Responsible for managing site selection and activation (IRB, agreements negotiations and legal review, etc)
  • Responsible for overseeing development of clinical databases, data management plans including data preparation, data validation activities, etc
  • Responsible for clinical site management
  • Develop monitoring plan and monitor sites for compliance with regulations
  • Act as clinical representative on cross-functional product development team
  • Complete clinical reports to support ISO and FDA requirements.
  • Support development of Clinical Evaluation Reports (CERs) as assigned
  • Process and review clinical study data using Good Clinical Practices (GCP) data-handling procedures and guidelines.
  • Coloplast employees are required to conduct business to the highest ethical and professional standards; comply with applicable laws and regulations, the MedTech Code of Conduct, and company policies.
  • Other duties as assigned

Basic Qualifications

  • 5-7 years of experience within clinical research, preferably with medical devices
  • Bachelor's degree (preferably in health science or biotech area)
  • Experience with clinical trial management, specifically - site activation, site management, monitoring and contract negotiation
  • Experience with ISO, FDA, GCP, and/or MedDev regulations and guidance for trial-related activities
  • Ability to travel: 20-30%

 

Required Knowledge, Skills and Abilities

  • Strong interpersonal and relationship-building skills
  • A collaborative mindset and strong motivation to make it easier for others to do great work
  • Ability to communicate with and drive efforts from external partners, such as health care providers
  • Self-driven with a structured and detail-oriented approach
  • Proficient in Microsoft Office applications including Word, Excel and PowerPoint

At Coloplast, we believe in recognizing and rewarding the contributions of our employees. Our total rewards package is designed to support your well-being, foster your professional growth, and ensure a healthy work-life balance. Here is some of what you can expect:

  • Health and Wellness: Comprehensive medical, dental, and vision insurance plans to keep you and your family healthy. Plus, access to company sponsored wellness programs and mental health resources, paid leave of absence for qualifying events and generous paid parental leave for both birthing and non-birthing parents.
  • Financial Security: A competitive 401(k) plan with company match that vest immediately, financial planning services to help you secure your future, and corporate discount programs for goods and services.
  • Work-Life Balance: Generous paid time off, flexible work hours, and flexible work arrangement options to help you balance your personal and professional life may be available.
  • Professional Development: Opportunities for continuous learning and career advancement through training programs, mentorship, and tuition reimbursement.
  • Recognition and Rewards: Recognition programs to celebrate achievements and contributions, including peer recognition, bonuses, awards, and special events.
  • Community and Culture: A supportive work environment where everyone feels valued, and has a sense of belonging.  Participate in team-building activities, volunteer opportunities, and company-sponsored events. Sustainability strategy that outlines our ambitions for how to run our company in a more sustainable way.
  • Competitive Compensation: The compensation range for this position is $108,191 - $162,287. Actual compensation is influenced by a variety of factors including but not limited to skills, experience, qualifications, and geographic location. Hired candidates may be eligible to receive additional compensation in the form of bonuses and/or incentives.

Pursuing an ambitious growth agenda, Coloplast develops and markets products and services that make life easier for people with intimate healthcare needs. Employing about 16,000 people and with products available in more than 143 countries, we are one of the worlds leading medical device companies. We are constantly growing our business and always looking for new ways to move forward - we explore, learn and look for new ways of doing things.

Visit us on Coloplast.com.

Watch the film. Follow us on LinkedIn.

Coloplast employees are required to conduct business to the highest ethical and professional standards; comply with applicable laws and regulations, the Advamed Code of Ethics on Interactions with Healthcare Professionals, and company policies.

Coloplast is committed to a policy of Equal Employment Opportunity (EEO) which means we employ and promote individuals based on their merits, regardless of race, color, religion, sex, national origin, age, disability, veteran status, pregnancy, sexual orientation, gender identity or expression, genetic information, marital status, citizenship status, status with regards to public assistance or any other protected classification.

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