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Medical Research Jobs in Florida (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 Assistants

Maitland, FL · On-site

$18 - $24.75/hr

At K2 Medical Research , we are transforming healthcare by delivering tomorrow's treatments today. As a rapidly growing clinical research organization across Florida, Tennessee, and Rhode Island, we ...

Research Assistants

Maitland, FL · On-site

$18 - $24.75/hr

At K2 Medical Research , we are transforming healthcare by delivering tomorrow's treatments today. As a rapidly growing clinical research organization across Florida, Tennessee, and Rhode Island, we ...

Clinical Research Coordinator

Ocala, FL · On-site

$21.25 - $28.25/hr

At K2 Medical Research, we are transforming healthcare by delivering tomorrow's treatments today. As a rapidly growing clinical research organization across Florida, Tennessee, and Rhode Island, we ...

Clinical Research Coordinator

Ocala, FL · On-site

$21.25 - $28.25/hr

At K2 Medical Research, we are transforming healthcare by delivering tomorrow's treatments today. As a rapidly growing clinical research organization across Florida, Tennessee, and Rhode Island, we ...

Clinical Research Coordinator

Lady Lake, FL · On-site

$21.25 - $28.25/hr

At K2 Medical Research, we are transforming healthcare by delivering tomorrow's treatments today. As a rapidly growing clinical research organization across Florida, Tennessee, and Rhode Island, we ...

Clinical Research Coordinators

Maitland, FL · On-site

$22.75 - $30/hr

At K2 Medical Research, we are transforming healthcare by delivering tomorrow's treatments today. As a rapidly growing clinical research organization across Florida, Tennessee, and Rhode Island, we ...

Clinical Research Coordinator

Lady Lake, FL · On-site

$21.25 - $28.25/hr

At K2 Medical Research, we are transforming healthcare by delivering tomorrow's treatments today. As a rapidly growing clinical research organization across Florida, Tennessee, and Rhode Island, we ...

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Showing results 1-20

Medical Research information

See Florida salary details

$28K

$39.9K

$43.7K

How much do medical research jobs pay per year?

As of Aug 31, 2026, the average yearly pay for medical research in Florida is $39,850.00, according to ZipRecruiter salary data. Most workers in this role earn between $40,400.00 and $43,300.00 per year, depending on experience, location, and employer.

What is medical research?

Medical research is the scientific study conducted to improve knowledge about health, diseases, treatments, and medical procedures. It involves clinical trials, laboratory experiments, and population studies to discover new ways to prevent, diagnose, and treat illnesses. Medical research can lead to the development of new medications, therapies, and medical devices, ultimately helping to improve patient care and public health. Researchers in this field often work in hospitals, universities, pharmaceutical companies, or government agencies.

What are medical research jobs?

Medical research jobs entail conducting research for the purpose of improving overall human health and saving lives. This is done by investigating diseases and possible methods of prevention and treatment, holding clinical trials using volunteer individuals or groups, and interpreting gathered data to prove or disprove hypotheses. Clinical research coordinators direct trials and work under a researcher or investigator. Clinical trial managers select and monitor the performance of clinical studies and products, and help train and hire CROs and study vendors. Other medical research jobs include clinical lab technicians and even microbiologists.

What are the key skills and qualifications needed to thrive in medical research, and why are they important?

To thrive in Medical Research, you need a solid background in biology, chemistry, or a related field, often supported by an advanced degree such as a Master's or Ph.D. and familiarity with research methodologies. Proficiency with statistical analysis software (e.g., SPSS, R), laboratory equipment, and compliance with regulatory standards like Good Clinical Practice (GCP) is crucial. Critical thinking, attention to detail, and strong written and verbal communication skills help researchers design robust studies and convey findings effectively. These competencies ensure research validity, regulatory compliance, and the advancement of medical knowledge to improve healthcare outcomes.

What are some common challenges faced by professionals in medical research, and how can they be addressed?

Medical research professionals often encounter challenges such as securing funding, managing complex regulatory requirements, and balancing multiple projects with tight deadlines. Adapting to rapidly evolving scientific methods and staying current with ethical guidelines are also essential. These challenges can be addressed by developing strong project management skills, collaborating closely with interdisciplinary teams, and actively seeking mentorship and professional development opportunities within the research community.

What is the difference between Medical Research vs Clinical Research?

AspectMedical ResearchClinical Research
CredentialsTypically requires degrees in medicine, biology, or related fields; certifications varyRequires degrees in health sciences, nursing, or related fields; often involves clinical trial certifications
Work EnvironmentLaboratories, research institutions, universitiesHospitals, clinics, clinical trial sites
Employer & Industry UsageUniversities, government agencies, biotech companiesPharmaceutical companies, hospitals, research organizations
Search & Comparison IntentUnderstanding basic scientific discoveries, lab-based workPatient-focused studies, drug testing, clinical trial processes

Medical Research involves studying diseases, treatments, and biological processes primarily in laboratory settings. Clinical Research focuses on testing new treatments and drugs directly with patients through clinical trials. While both roles aim to improve healthcare, Medical Research is more lab-oriented, whereas Clinical Research is patient-centered and involves real-world testing.

How to work as a medical researcher?

To work as a medical researcher, typically a bachelor's degree in a health-related field is required, with advanced roles often requiring a master's or doctoral degree such as a Ph.D. or M.D. Additionally, skills in data analysis, laboratory techniques, and familiarity with research tools are essential, along with experience in clinical or laboratory settings. Certification or training in research ethics and good clinical practice can also enhance employment prospects.

What is a career in medical research?

A career in medical research involves studying diseases, treatments, and health conditions to develop new medical knowledge and improve patient care. Professionals in this field often work in laboratories or clinical settings, utilizing skills in data analysis, laboratory techniques, and scientific communication, and may require advanced degrees such as a master's or Ph.D.

What are the most commonly searched types of Medical Research jobs in Florida?

The most popular types of Medical Research jobs in Florida are:

What are popular job titles related to Medical Research jobs in Florida?

For Medical Research jobs in Florida, the most frequently searched job titles are:

What cities in Florida are hiring for Medical Research jobs?

Cities in Florida with the most Medical Research job openings:

Infographic showing various Medical Research job openings in Florida as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, and 5% Contract. Highlights an 87% Physical, 1% Hybrid, and 12% Remote job distribution, with an average salary of $39,850 per year, or $19.2 per hour.

Medical Research Consultant

Jacksonville, FL • Remote

ARC Group
11 - 50 employees

Full-time

Re-posted 20 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.