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Remote Clinical Trials Test Subject Jobs (NOW HIRING)

Adecco

Clinical Trials Manager- Remote

Chapel Hill, NC · Remote

$62 - $64.73/hr

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of ... An employer who violates this law shall be subject to criminal penalties and civil liability.

Natera

Manager, Clinical Trials

$115K - $144K/yr

The Clinical Trial Manager should have experience in managing all aspects of the trials ... Remote USA $115,800-$144,700 USD OUR OPPORTUNITY Natera™ is a global leader in cell-free DNA ...

Natera

Senior Manager, Clinical Trials

OR · On-site +1

This Senior Manager, Clinical Trial is responsible for managing all aspects of clinical trials to support the development, validation, and commercialization non-invasive molecular diagnostic tests.

Natera

Senior Manager, Clinical Trials

$141K - $176K/yr

... tests. This role manages clinical operations staff and all aspects of the trials independently ... Remote USA $141,300-$176,600 USD OUR OPPORTUNITY Natera™ is a global leader in cell-free DNA ...

Gilead

Sr Clinical Trials Manager

Foster City, CA · On-site +1

$157K - $203K/yr

Will not consider fully remote candidates. Responsibilities: * Lead all aspects of assigned ... Eligible employees may participate in benefit plans, subject to the terms and conditions of the ...

Round Rock High School

Clinical Trials Medical Writer

$77K - $92K/yr

Remote East Coast | Must Sit in East Coast Hours Per Week: 40 hours Schedule: Days, Monday - Friday ... Serve as a subject-matter expert (SME) for medical documentation utilized throughout the study ...

Gilead

Sr Clinical Trials Manager

Foster City, CA · On-site +1

$157K - $203K/yr

Will not consider fully remote candidates. Responsibilities: * Lead all aspects of assigned ... Eligible employees may participate in benefit plans, subject to the terms and conditions of the ...

COPD Foundation

$80K/yr

Position Overview The Assistant Director of Clinical Trials Network reports to the Senior Director ... Ability to work effectively both independently and collaboratively in a remote environment.

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Remote Clinical Trials Test Subject information

What is a remote clinical trials test subject?

Remote clinical trials test subjects are individuals who participate in medical research studies from their own homes or other locations outside of traditional clinical settings. These participants help researchers evaluate the safety and effectiveness of new treatments, drugs, or medical devices. The process typically involves following study protocols, attending virtual appointments, and reporting symptoms or side effects, often using digital tools or wearable devices. Remote participation makes clinical trials more accessible and convenient for a wider range of people while maintaining rigorous scientific standards.

What skills and qualifications are needed to thrive as a remote clinical trials test subject?

To thrive as a Remote Clinical Trials Test Subject, you should have a basic understanding of study protocols, the ability to follow instructions precisely, and may need to meet specific health or demographic criteria. Familiarity with telemedicine platforms, secure data entry systems, and remote monitoring devices is often required. Reliability, clear communication with research staff, and attention to detail are crucial soft skills for this role. These skills ensure accurate data collection, participant safety, and the overall integrity of the clinical trial.

What are common challenges faced by remote clinical trials test subjects, and how can they be addressed?

Remote clinical trials test subjects may encounter challenges such as adhering to strict study protocols from home, managing frequent self-reporting tasks, and ensuring timely communication with research staff. To address these, participants should establish a consistent routine for study-related activities, use provided digital tools for reminders and data submission, and proactively reach out to coordinators if questions or issues arise. Reliable internet access and a quiet space can also help facilitate a smoother experience throughout the trial.

What cities are hiring for Remote Clinical Trials Test Subject jobs?

Cities with the most Remote Clinical Trials Test Subject job openings:

What are the most commonly searched types of Clinical Trials Test Subject jobs?

The most popular types of Clinical Trials Test Subject jobs are:

What states have the most Remote Clinical Trials Test Subject jobs?

States with the most job openings for Remote Clinical Trials Test Subject jobs include:

Remote Clinical Trials Test Subject jobs near you

Clinical Trials Manager- Remote

Adecco

Chapel Hill, NC • Remote

$62 - $64.73/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 24 days ago

Key responsibilities

  • Manage clinical operational and quality activities for assigned studies in compliance with ICH/GCP and applicable regulations.

  • Develop and maintain clinical tools, monitoring plans, guidelines, and study documentation.

  • Monitor clinical timelines, metrics, site performance, and study progress.

Job description

Clinical Trials Manager (CTM)

Location: Remote
Schedule: Full-Time | Eastern Time Zone Hours
Pay: $62.00–$64.73 per hour

Position Overview

We are seeking an experienced Clinical Trials Manager (CTM) to oversee the clinical operational and quality aspects of assigned clinical studies. This role is responsible for ensuring clinical deliverables are completed on time, within scope, and to quality standards, while supporting patient recruitment, study performance, and overall trial execution.

The ideal candidate will have strong clinical operations experience, excellent leadership and organizational skills, and a solid understanding of ICH/GCP, FDA regulations, clinical monitoring, and patient recruitment strategies.

Key Responsibilities

  • Manage clinical operational and quality activities for assigned studies in compliance with ICH/GCP and applicable regulations.

  • Develop and maintain clinical tools, monitoring plans, guidelines, and study documentation.

  • Support development and maintenance of the Trial Master File (TMF) and ensure document quality and completeness.

  • Collaborate with Project Managers, clinical teams, data management, and other departments to meet study deliverables.

  • Lead clinical team meetings and ensure timelines, resources, communication, and quality objectives are maintained.

  • Monitor clinical timelines, metrics, site performance, and study progress.

  • Review monitoring reports, oversee CRF collection and query resolution, and implement recovery actions when needed.

  • Support patient recruitment strategies and work with study sites to address recruitment and retention challenges.

  • Communicate with study sites regarding protocol requirements, patient participation, CRFs, and study-related issues.

  • Coordinate study start-up activities and support timely ethics committee and regulatory submissions.

  • Ensure essential documents meet regulatory and quality requirements.

  • Support clinical resource planning, delegation of responsibilities, and identification of additional staffing needs.

  • Provide regular project status updates and contribute to client meetings and presentations.

  • Support forecasting, budgeting, and management of clinical project resources.

  • Ensure timely archiving of study documents and materials.

Qualifications

  • Bachelor's degree or equivalent relevant education.

  • 5+ years of relevant clinical research/clinical operations experience or comparable experience.

  • Strong understanding of ICH/GCP, FDA guidelines, and clinical trial requirements.

  • Experience with clinical monitoring practices and study operations.

  • Demonstrated experience with patient recruitment and retention strategies.

  • Strong leadership, mentoring, and team-building skills.

  • Excellent planning, organization, and prioritization abilities.

  • Strong problem-solving, judgment, and decision-making skills.

  • Ability to work effectively in a multicultural, matrixed, and changing environment.

  • Strong written and verbal communication skills.

  • Excellent attention to detail and ability to manage multiple priorities.

  • Working knowledge of Outlook, Excel, Word, and clinical research systems.

  • Understanding of budgeting, forecasting, resource allocation, and financial management preferred.

Work Arrangement

  • 100% Remote

  • Must be available to work Eastern Time Zone hours.

  • Full-time position.

Pay Rate: $62.00–$64.73/hour


Pay Details: $62.00 to $64.73 per hour
Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs. In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.
Equal Opportunity Employer/Veterans/Disabled
Military connected talent encouraged to apply
To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to https://www.adecco.com/en-us/candidate-privacy
The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable:
  • The California Fair Chance Act
  • Los Angeles City Fair Chance Ordinance
  • Los Angeles County Fair Chance Ordinance for Employers
  • San Francisco Fair Chance Ordinance

Massachusetts Candidates Only: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.