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Medical Research Consultant Jobs (NOW HIRING)

MEDICAL RESEARCH CONSULTANT REMOTE ARC Group has an immediate opportunity for a Medical Research Consultant! This is a direct hire FTE position, 100% remote. This is a fantastic opportunity to join ...

Research Consultant V

New York, NY ยท On-site

$66 - $86/hr

Title: Research Consultant Location: 100% Remote Compensation: $66 - $86 Work Requirements: US ... Comprehensive medical benefits * Competitive pay * 401(k) Retirement plan * ...and much more! About ...

... Consultant. This position provides hands-on experience in candidate sourcing, outreach, and ... Professionalism and confidence to effectively communicate with medical professionals and hospital ...

... Consultant. This position provides hands-on experience in candidate sourcing, outreach, and ... Professionalism and confidence to effectively communicate with medical professionals and hospital ...

Consultant, Primary Research

Chicago, IL ยท On-site

$55K - $68K/yr

The Consultant, Primary Research is responsible for designing, executing, and delivering custom ... Alongside salary, Mintel offers a comprehensive benefits package including medical/dental/vision ...

Consultant, Primary Research

Chicago, IL ยท On-site

$55K - $68K/yr

The Consultant, Primary Research is responsible for designing, executing, and delivering custom ... Alongside salary, Mintel offers a comprehensive benefits package including medical/dental/vision ...

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Medical Research Consultant information

See salary details

$31K

$148.2K

$399K

How much do medical research consultant jobs pay per year?

As of Aug 3, 2026, the average yearly pay for medical research consultant in the United States is $148,159.00, according to ZipRecruiter salary data. Most workers in this role earn between $97,500.00 and $181,500.00 per year, depending on experience, location, and employer.

What does a medical research consultant do?

A Medical Research Consultant provides expert guidance and support to organizations or research teams conducting medical or clinical studies. Their responsibilities include designing research protocols, analyzing data, ensuring compliance with ethical standards, and helping interpret study results. They often advise on best practices in clinical trials, regulatory requirements, and the latest advances in medical science. This role is crucial for ensuring that medical research projects are scientifically sound and aligned with industry standards.

What is the difference between Medical Research Consultant vs Clinical Research Associate?

AspectMedical Research ConsultantClinical Research Associate
Required CredentialsMedical degree or relevant healthcare certification, research experienceLife sciences degree, clinical research training, certification often preferred
Work EnvironmentConsulting firms, healthcare organizations, research institutionsPharmaceutical companies, CROs, clinical trial sites
Employer & Industry UsageUsed in healthcare consulting, research planning, and advisory rolesInvolved in monitoring and managing clinical trial sites
Common Search & Comparison IntentUnderstanding roles in medical research consultingClarifying clinical trial monitoring responsibilities

Medical Research Consultants focus on advising and planning research projects, often with a healthcare or academic background. Clinical Research Associates primarily oversee clinical trial sites, ensuring compliance and data integrity. Both roles require research knowledge but differ in scope and daily tasks.

How does a medical research consultant typically collaborate with clinical teams and stakeholders during a research project?

Medical Research Consultants often act as liaisons between research teams, clinical staff, and external stakeholders. They facilitate communication to ensure research protocols are understood and followed, provide expert guidance on study design, and help interpret data for clinical relevance. Regular meetings and updates are common, as consultants work closely with principal investigators, sponsors, and regulatory bodies to keep projects aligned with objectives and compliance requirements. This collaborative approach is essential for translating research findings into actionable healthcare solutions.

What are the key skills and qualifications needed to thrive as a medical research consultant?

To thrive as a Medical Research Consultant, you need a solid background in biomedical sciences, research methodologies, and data analysis, typically supported by an advanced degree such as a PhD or MD. Familiarity with statistical software (e.g., SPSS, R), literature databases, and regulatory compliance systems is essential. Exceptional critical thinking, communication, and project management skills distinguish top performers in this role. These capabilities ensure high-quality research outcomes, effective stakeholder collaboration, and compliance with industry standards.
More about Medical Research Consultant jobs
Infographic showing various Medical Research Consultant job openings in the United States as of July 2026, with employment types broken down into 1% Locum Tenens, 1% As Needed, 87% Full Time, 7% Part Time, and 4% Contract. Highlights an 88% Physical, 4% Hybrid, and 8% Remote job distribution, with an average salary of $148,159 per year, or $71.2 per hour.

Medical Research Consultant

ARC Group

Jacksonville, FL โ€ข Remote

Full-time

Re-posted 22 days ago


Job description

MEDICAL RESEARCH CONSULTANT REMOTE
ARC Group has an immediate opportunity for a Medical Research Consultant! This is a direct hire FTE position, 100% remote. This is a fantastic opportunity to join an established and well-respected organization offering tremendous career growth potential and an outstanding benefits package.
At ARC Group, we are committed to fostering a diverse and inclusive workplace where everyone feels valued and respected. We believe that diverse perspectives lead to better innovation and problem-solving. As an organization, we embrace diversity in all its forms and encourage individuals from underrepresented groups to apply.
100% REMOTE!
Candidates must have permanent work authorization and work for any employer without sponsorship now or in the future. Third party candidates are not eligible for this role.
SUMMARY STATEMENT
Under limited direction, this position is responsible for providing central research coordination for the Medical Affairs department, which is the primary clinical decision-support and medical policy-making organization within the enterprise, which operates as Medicare Administrative Contractor. Accountabilities include identification, receipt, tracking, review, analysis, and recommendation regarding evidence for topics under consideration for development or revision of a Local Coverage Determination (LCD) or other action by the Medical Policy team. Medical Research Consultants are responsible for conducting comprehensive literature searches and reviews to support evidence-based decision making within the organization. They play a crucial role in synthesizing research findings from diverse sources to provide clear and actionable insights.
ESSENTIAL DUTIES & RESPONSIBILITIES
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. This list of essential job functions is not exhaustive and may be supplemented as necessary.
Research: Literature analysis, health technology assessment
* Conduct Comprehensive Literature Searches -- 20%
o Identify relevant research articles utilizing various databases such as PubMed, Cochrane, and Embase
o Screen titles, abstracts, and full-text articles for inclusion based on predefined criteria
o Lead the development and revision of PICOT (patient, intervention, comparison, outcome, and time) questions for each LCD project.
* Data Assessment -- 35%
o Extract relevant data from included studies, ensuring accuracy and consistency
o Review statistical data, assess the quality and risk of bias in individual studies using standardized tools
o Perform meta-analyses or qualitative synthesis, as appropriate, to combine study findings
o Compile unbiased findings in clear, concise, and actionable reports, complete with tables, figures, and appendices.
o Creation of synthesis workbook for each LCD project.
o Creation of Evidence Review Table for each Contractor Advisory Committee topic.
* Communication and Collaboration -- 20%
o Collaborate with interdisciplinary teams, actively presents findings and recommendations for consideration and discussion
o Routinely interacts with various levels of staff within the company, including the Contractor Medical Directors (CMDs), management, and routine communications with the Medical Policy team
o Based on evidentiary reviews, propose policy decisions and coverage determinations for products and treatments to the policy development team to be implemented via LCDs.
o Serve as liaison during national workgroup meetings, representing the company and sharing information to ensure that research methodologies and coverage determinations are consistent
o Serve as point of contact and SME for internal operations including the CMDs and senior leadership regarding research methodologies and related tasks.
* Policy Writing -- 20%
o Development of summary and analysis of evidence for inclusion in LCDs to support coverage/noncoverage determinations.
o Active collaborator in the policy writing and determination process, assisting with coverage/non-coverage determination verbiage, review of proposed and final LCDs, and revision recommendations.
o Actively collaborates with the policy nurse to address the evidence portion of the LCD Analyses.
* Operationalization and Training -- 5%
o Continually update knowledge of systematic review methods, guidelines, and best practices
o Provide training and mentorship to junior staff or team members on systematic review methodologies
o Contribute to standardizing deliverables (e.g., templates) and health technology assessment process
Performs other duties as the supervisor may, from time to time, deem necessary.
REQUIRED QUALIFICATIONS
*Master's in Public Health, Epidemiology, Health Sciences, Data Science, or a related field
*Demonstrated proficiency in MS Office applications
*Demonstrated proficiency in systematic review software tools (e.g., RevMan, DistillerSR, Covidence)
*Demonstrated experience conducting systematic reviews and meta-analyses
*Demonstrated experience and confidence leading a large group meeting
*Demonstrated project management experience
*Detail-oriented with a commitment to producing high-quality work
*Demonstrated excellent written and verbal communication
*Demonstrated excellent organization and tracking skills
*Demonstrated excellent collaboration ability
*Demonstrated strong analytical and critical thinking
*Demonstrated ability to work both independently and collaboratively in a team environment
*Ability to work effectively in a collaborative environment with the Medical Policy team including active participation in meetings, presentation of findings, and respond effectively to questions
PREFERRED QUALIFICATIONS
*Ph.D. in Public Health, Epidemiology, Health Sciences, Data Science, or a related field
*Two years of related experience
*Knowledge of PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines
*Experience with GRADE (Grading of Recommendations, Assessment, Development, and Evaluations) methodology
*Familiarity with statistical software (e.g., Stata, R)
ARC Group is a Forbes-ranked a top 20 recruiting and executive search firm working with clients nationwide to recruit the highest quality technical resources. We have achieved this by understanding both our candidate's and client's needs and goals and serving both with integrity and a shared desire to succeed.
At ARC Group, we are committed to providing equal employment opportunities and fostering an inclusive work environment. We encourage applications from all qualified individuals regardless of race, ethnicity, religion, gender identity, sexual orientation, age, disability, or any other protected status. If you require accommodations during the recruitment process, please let us know.
No fee to candidate.