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Relocation Clinical Trials Jobs (NOW HIRING)

Exelixis

Clinical Trials Manager (Oncology)

Alameda, CA · On-site

Full relocation provided ESSENTIAL DUTIES AND RESPONSIBILITIES: Manages clinical trials, including those conducted through Contract Research Organizations (CROs) May participate in developing and ...

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How much do relocation clinical trials jobs pay per hour?

As of Jun 6, 2026, the average hourly pay for relocation clinical trials in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Clinical Trials Relocation Specialist, and why are they important?

To thrive as a Clinical Trials Relocation Specialist, you need expertise in clinical research processes, project management, and regulatory compliance, often supported by a degree in life sciences or healthcare. Familiarity with clinical trial management systems (CTMS), ICH-GCP guidelines, and logistics tracking tools is typically required. Strong organizational, communication, and problem-solving skills are essential for coordinating trial site moves and supporting research teams. These competencies ensure successful trial relocation, regulatory adherence, and minimal disruption to clinical operations.

What are some common challenges faced when coordinating relocation for clinical trial participants, and how can these be managed effectively?

Coordinating relocation for clinical trial participants often involves challenges such as managing logistics, ensuring compliance with regulatory requirements, and addressing participants' personal needs. Effective management requires strong organizational skills, clear communication with both participants and cross-functional teams, and thorough knowledge of trial protocols and local regulations. Building trust and providing personalized support can help participants adjust smoothly, while close collaboration with site staff, travel coordinators, and healthcare professionals ensures a seamless relocation process.

What are Relocation Clinical Trials?

Relocation clinical trials are research studies that involve moving participants or clinical trial operations from one location to another. This can happen for various reasons, such as access to specialized facilities, regulatory requirements, or participant convenience. The process involves careful planning to ensure the safety and integrity of the trial data while maintaining compliance with ethical and legal standards. Relocation may also include providing support to participants, such as housing or travel arrangements. These trials are crucial for advancing medical knowledge and improving patient care, especially when specialized resources are needed.

What is the difference between Relocation Clinical Trials vs Clinical Research Coordinator?

AspectRelocation Clinical TrialsClinical Research Coordinator
CredentialsTypically requires clinical trial experience, sometimes certifications like CCRPRequires clinical research experience, often with certifications like CCRP or CCRC
Work EnvironmentConducts multi-site or international trials, often traveling or coordinating across locationsWorks mainly at research sites or hospitals, managing local trial activities
Employer & IndustryPharmaceutical companies, CROs, research institutionsHospitals, clinics, research centers

Relocation Clinical Trials involve managing and coordinating clinical studies across multiple locations or countries, often requiring travel and international collaboration. Clinical Research Coordinators focus on local trial management at specific sites. Both roles require similar certifications and work within the clinical research industry, but their scope and environment differ.

Infographic showing various Relocation Clinical Trials job openings in the United States as of May 2026, with employment types broken down into 100% Full Time. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.
CLINICAL TRIALS SCREENING COORDINATOR I

CLINICAL TRIALS SCREENING COORDINATOR I

H. Lee Moffitt Cancer Center

Tampa, FL • On-site

$28.34 - $35.57/hr

Full-time

Posted 22 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

72nd of 867 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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