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Medical In Clinical Trials Jobs (NOW HIRING)

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Clinical Trials Operations Specialist Qualifications: * 1-2+ years of patient-facing experience in clinical research, healthcare, or a related medical setting * 2+ years in a clinical role such as ...

Clinical Trials Recruiter

Brooklyn, NY · On-site +1

$20 - $30/hr

About Us We are a dedicated clinical research site committed to advancing medical knowledge through ... Previous experience in patient recruitment, sales, customer service, or healthcare preferred.

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How much do medical in clinical trials jobs pay per hour?

As of Jun 11, 2026, the average hourly pay for medical in clinical trials in the United States is $20.45, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $22.12 per hour, depending on experience, location, and employer.

What is the difference between Medical In Clinical Trials vs Clinical Research Coordinator?

AspectMedical In Clinical TrialsClinical Research Coordinator
CredentialsMedical degree or relevant healthcare certificationBachelor's degree, often in health or science fields
Work EnvironmentHospitals, clinics, research centersResearch sites, hospitals, clinics
Employer & IndustryPharmaceutical companies, CROs, academic institutionsResearch organizations, hospitals, clinics
Primary FocusOverseeing patient care and medical procedures in trialsManaging study logistics, data collection, and compliance

Medical In Clinical Trials typically involves direct patient care and medical oversight during clinical studies, requiring healthcare credentials. In contrast, Clinical Research Coordinators focus on managing study operations and data. Both roles are essential in clinical research but differ in responsibilities and qualifications.

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What cities are hiring for Medical In Clinical Trials jobs? Cities with the most Medical In Clinical Trials job openings:
What states have the most Medical In Clinical Trials jobs? States with the most job openings for Medical In Clinical Trials jobs include:
Infographic showing various Medical In Clinical Trials job openings in the United States as of June 2026, with employment types broken down into 1% Locum Tenens, 4% As Needed, 41% Full Time, 29% Part Time, 2% Temporary, and 23% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $42,540 per year, or $20.5 per hour.
CLINICAL TRIALS SCREENING COORDINATOR I

CLINICAL TRIALS SCREENING COORDINATOR I

H. Lee Moffitt Cancer Center

Tampa, FL • Hybrid

Full-time

Posted 26 days ago


Moffitt Cancer Center rating

8.1

Company rating: 8.1 out of 10

Based on 92 frontline employees who took The Breakroom Quiz

70th of 870 rated healthcare providers


Job description

Job Summary

 

Are you looking for an opportunity to impact lives and be a central part of a dynamic and innovative team in the fight against cancer? As a Moffitt Clinical Research Coordinator, you’ll bring hope to patients by delivering tomorrow’s cancer treatments today! You will have the opportunity to interact directly with patients, enroll, educate and guide them through the experiences of taking part in clinical trials while receiving innovative treatments as part of a therapeutic clinical trial. You will be the member of the Team that ensures the trial is moving forward safely, smoothly, and according to plan. 

Our Clinical Research Coordinators come from a variety of backgrounds and experiences, including social sciences (public health, social work, sociology, psychology, communications, and more), biological sciences, business, and humanities. The Clinical Research Coordinator role is a terrific opportunity for those who have already worked in other areas of healthcare as well as those who are looking for a new and exciting way to contribute through their career.  

This position offers a Monday through Friday schedule and hybrid work (mix of remote and on-site) after passing a 90-day introductory and training period. Moffitt offers paid training and orientation through its CTO (Clinical Trails Office) Academy. Position tiers may vary according to experience. Relocation assistance may be provided. 

https://moffitt.org/clinical-trials-research/clinical-trials/clinical-trials-administration/ 

Clinical Trials 

These positions work closely with patients, patient families, study sponsors (from smaller pioneer biotech companies through large pharmaceutical companies), and the Clinical Trial Team that includes physicians, pharmacists, nurses, data monitors and data managers.  

Successful candidates will possess: 

  • Effective communication, good decision-making, eagerness to embrace challenges with a sense of urgency and enthusiasm, and time management skills 
  • Excellent teamwork skills and ability to collaborate with those from diverse backgrounds and experiences 
  • Prior experience in clinical trials is preferred 
  • Familiarity with regulatory requirements in clinical research or ability to successfully learn this  
  • Experience interacting with patients and coordinating care with medical staff 
  • Gain a solid learning and understanding of regulatory guidelines and following a clinical trial protocol

Job Summary

The Clinical Trials Screening Coordinator I reports to the Clinical Trials Office but will directly support a specific Disease Site Program. This position is embedded in the clinic to serve as a single point of contact to aid physicians, clinical team - members and research personnel with timely identification of patients for consideration for clinical trial enrollment. The role performs an integrated approach to ensure effectiveness and efficiencies for directing potential patients to a trial program. The role has the primary responsibility for referring physicians, patients and caregivers to guide, review eligibility and provide access to available clinical trials. This is role is within the clinical trials career path supporting the PI in clinical trials.

Minimum Requirements

Bachelor's degree in science, health-related field or related project management. 

2 years' experience in clinical trials (patient-facing coordination, data management, regulatory or other research coordination).


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