2

Remote Clinical Investigator Jobs (NOW HIRING)

Must have experience in GCP auditing: clinical report, clinical investigational site, clinical ... When indicated perform or supervise remote vendor audits and provide follow-up as indicated

Those fully remote associates residing in states where service is required by contract, law, or ... Clinical Experience preferred * SIU and/or State Medicaid regulatory compliance work experience ...

Those fully remote associates residing in states where service is required by contract, law, or ... Clinical Experience preferred * SIU and/or State Medicaid regulatory compliancework experience ...

Overview Senior Clinical Research Associate US Remote Emmes Group: Building a better future for us ... Participates in Investigator Meetings or other client meetings as needed. * Assists with filing and ...

next page

Showing results 1-20

Remote Clinical Investigator information

See salary details

$35K

$56.1K

$101K

How much do remote clinical investigator jobs pay per year?

As of Jul 3, 2026, the average yearly pay for remote clinical investigator in the United States is $56,057.00, according to ZipRecruiter salary data. Most workers in this role earn between $46,500.00 and $47,000.00 per year, depending on experience, location, and employer.

What does the typical workday look like for a Remote Clinical Investigator?

As a Remote Clinical Investigator, your day often includes reviewing clinical trial data, ensuring protocol compliance, and conducting remote site monitoring visits via video calls or secure digital platforms. You'll communicate regularly with study coordinators, sponsors, and regulatory agencies to resolve queries and address study-related issues. Documentation, data verification, and ongoing training to stay updated with regulations are also part of the workflow. This role offers flexibility and autonomy, but requires excellent organization to manage multiple studies and deadlines from a home or remote office environment.

What is a Remote Clinical Investigator job?

A Remote Clinical Investigator is responsible for overseeing and analyzing clinical trial data, ensuring compliance with regulatory standards, and monitoring patient safety—all while working remotely. They collaborate with research teams, healthcare professionals, and regulatory bodies to assess trial integrity and effectiveness. Their duties may include reviewing medical records, identifying adverse events, and ensuring protocol adherence. This role requires strong analytical skills, clinical knowledge, and experience in research or regulatory compliance.

What are the key skills and qualifications needed to thrive in the Remote Clinical Investigator position, and why are they important?

To excel as a Remote Clinical Investigator, you need a strong background in clinical research, data analysis, and regulatory compliance, usually supported by a degree in a health-related field. Familiarity with electronic data capture systems, Good Clinical Practice (GCP) certification, and experience using remote monitoring tools are highly valued. Exceptional organizational skills, attention to detail, and effective written and verbal communication are standout soft skills for this role. These competencies ensure rigorous study conduct, accurate data collection, and clear collaboration with sponsors, study sites, and regulatory bodies.

More about Remote Clinical Investigator jobs
What cities are hiring for Remote Clinical Investigator jobs? Cities with the most Remote Clinical Investigator job openings:
What are the most commonly searched types of Clinical Investigator jobs? The most popular types of Clinical Investigator jobs are:
What states have the most Remote Clinical Investigator jobs? States with the most job openings for Remote Clinical Investigator jobs include:
Infographic showing various Remote Clinical Investigator job openings in the United States as of June 2026, with employment types broken down into 26% Full Time, 48% Part Time, 24% Contract, and 2% Nights. Highlights an 37% Physical, 3% Hybrid, and 60% Remote job distribution, with an average salary of $56,057 per year, or $27 per hour.

MD/DO Consultant - Principal Investigator - Conroe, Texas

Hawthorne Health

Conroe, TX • On-site, Remote

Contractor

Posted 2 days ago

Be an early applicant


Job description

About Us 
Hawthorne Health is a leading community site network and home research visit solution provider, with 20+ sites and more than 2,000 research experienced healthcare professionals across the U.S. Hawthorne leverages convenient, trusted, healthcare locations, identified patient data, and intelligent technology to accelerate patient access, improve retention, and reduce study costs. By embedding high-quality research within local communities, Hawthorne makes clinical trials more accessible and convenient for patients. Our community-based model shortens timelines and helps bring better treatments to market, faster. 
 
About the Role
Hawthorne Health is seeking an experienced, Principal Investigator MD on a 1099 contract opportunity to join our growing team and lead the investigation for our new site in Conroe, TX. 
Responsibilities
  • Accurately document findings and contribute to ongoing clinical trials, registries, or research protocols as applicable.
  • Oversee and manage all aspects of clinical trials conducted at the research site, ensuring adherence to the study protocol, Good Clinical Practice (GCP), ICH guidelines, and all applicable regulatory requirements.
  • Lead and supervise the clinical research team, including sub-investigators, study coordinators, and other site staff.
  • Delegate study-related duties appropriately to qualified personnel and ensure proper training and oversight.
  • Conduct remote review of patient assessments, including physical exams, medical histories, and eligibility screenings, to ensure appropriate participant enrollment.
  • Review and interpret laboratory results, ECGs, and other diagnostic tests.
  • Make critical medical decisions regarding participant care, adverse events, and protocol deviations.
  • Ensure accurate, complete, and timely collection and documentation of all study data.
  • Communicate effectively with sponsors, Contract Research Organizations (CROs), Institutional Review Boards (IRBs), and regulatory authorities.
  • Manage investigational product accountability, storage, and administration according to protocol and with the help of the on-site IP team.
  • Participate in site initiation visits, monitoring visits, audits, and inspections.
  • Maintain continuous medical education and stay current with advancements in clinical research and relevant therapeutic areas.
Requirements
  • Experience as a Principal Investigator on at least 3 sponsor initiated clinical trials.
  • Medical Doctor (M.D. or equivalent) degree from an accredited institution.
  • Current, unrestricted medical license.
  • Board certification in a relevant specialty preferred.
  • Demonstrated in-depth knowledge of ICH-GCP guidelines, FDA regulations, and other relevant ethical and regulatory requirements for clinical research.
  • Proven leadership and team management skills.
  • Excellent clinical judgment and decision-making abilities.
  • Strong verbal and written communication skills in English, with the ability to present complex information clearly and concisely.
  • Exceptional organizational skills and meticulous attention to detail.
  • Ability to manage multiple complex studies simultaneously and prioritize tasks effectively.
  • Commitment to ethical conduct and patient safety.
Location & Time Commitment
  • 3-5 hours per week of remote clinical oversight.
  • This position requires being on site in Conroe, TX ~2 times per month for key visits. 
Position Type: Part-time, 1099 contract
Compensation: Hourly; rate negotiable based on experience
Hawthorne Health is transforming the clinical trial landscape through an innovative site model that integrates research into community-based settings like local pharmacies. By meeting patients where they already receive care, we are improving access, strengthening trust, and driving more inclusive and efficient trials.
 
We welcome the opportunity to connect with individuals interested in being part of this evolving mode

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.To view our privacy policy and terms of use, please use the links below. Privacy Policy: https://hawthornehealth.com/privacy-policy/Terms of Use: https://hawthornehealth.com/terms-of-use/