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Temporary Weekend Clinical Research Jobs (NOW HIRING)

Clinical Research Coordinator 1

Miami, FL

$23.25 - $30.75/hr

If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click ... Ability to work evenings, nights, and weekends as necessary. * Commitment to the University's core ...

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Clinical Research Coordinator (CRC I) - Pediatric & Vaccine Studies Layton & Murray, Utah $25.00 ... Our positions are not temporary or contract, they are direct hire with full benefits. Our purpose ...

Job Title: Clinical Research Coordinator This position offers an experienced Clinical Research ... If eligible, the benefits available for this temporary role may include the following: • Medical ...

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Job Title: Part-Time Clinical Research Coordinator Hours: 20 per week (flexible Monday-Friday ... If eligible, the benefits available for this temporary role may include the following: • Medical ...

Clinical Research Coordinator This role coordinates and manages all aspects of clinical research ... If eligible, the benefits available for this temporary role may include the following: • Medical ...

Clinical Research Coordinator 1

Miami, FL · On-site

$23.25 - $30.75/hr

If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click ... Ability to work evenings, nights, and weekends as necessary. Commitment to the University's core ...

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Temporary Weekend Clinical Research information

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$12

$41

$69

How much do temporary weekend clinical research jobs pay per hour?

As of Jun 13, 2026, the average hourly pay for temporary weekend clinical research in the United States is $41.13, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $52.64 per hour, depending on experience, location, and employer.

What is the difference between Temporary Weekend Clinical Research vs Temporary Weekend Clinical Data Coordinator?

AspectTemporary Weekend Clinical ResearchTemporary Weekend Clinical Data Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related field; some roles may need clinical research certificationsRequires a bachelor's degree in health informatics, data management, or related field; certifications like CDMP are a plus
Work EnvironmentResearch sites, hospitals, or clinics conducting clinical trialsData management departments within research organizations or hospitals
Employer & Industry UsagePharmaceutical companies, CROs, academic research institutionsResearch organizations, hospitals, clinical trial sponsors

Temporary Weekend Clinical Research involves assisting with clinical trials, patient interactions, and trial procedures during weekends. In contrast, Temporary Weekend Clinical Data Coordinators focus on managing and ensuring the accuracy of trial data. Both roles often require similar educational backgrounds but differ in daily responsibilities and focus areas within the clinical research industry.

What cities are hiring for Temporary Weekend Clinical Research jobs? Cities with the most Temporary Weekend Clinical Research job openings:
What are the most commonly searched types of Weekend Clinical Research jobs? The most popular types of Weekend Clinical Research jobs are:
What states have the most Temporary Weekend Clinical Research jobs? States with the most job openings for Temporary Weekend Clinical Research jobs include:
Clinical Research Coordinator 1

$23.25 - $30.75/hr

Full-time

Medical, Dental

Posted 6 hours ago


University Of Miami rating

7.7

Company rating: 7.7 out of 10

Based on 52 frontline employees who took The Breakroom Quiz

216th of 536 rated colleges and universities


Job description

Current Employees:

If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click here to log in to Workday to use the internal application process. To learn how to apply for a faculty or staff position, please review this tip sheet.

The Clinical Translational Research Site is currently seeking a full time Clinical Research Coordinator 1 to work in Miami. The Clinical Research Coordinator 1 serves as an entry level clinical research professional that has a basic foundation in clinical research through assigned responsibilities in data management or implementing clinical research protocols. This role exhibits increased learned skills and flexibility in performing duties and assumes responsibility for simple clinical research protocols and timelines.

CORE RESPONSIBILITIES:

  • Performs chart review/pre-screening activities for study participant eligibility and coordination of simple clinical research protocols. Maintains enrollment procedures according to the protocol.

  • Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, schedules appointments and study visits, meeting scheduling, and project evaluation.

  • Performs moderate to complex research tests/ experiments and adapts procedures for quality improvement under supervision.

  • Understands and follows technical instructions for operating clinical research equipment, problem solves when operational failures occur.

  • Assists in observing and informing the PI/supervisor of adverse events, including those reported by study participants.

  • Addresses adverse events per protocol, advocating for study participants and quality standards throughout the lifespan of the study.

  • Identifies, reports, and helps problem solve protocol deviations and unanticipated occurrences.

  • Follows the appropriate fundamental requirements of all international, national, and local regulatory bodies.

  • Knows the contents and maintenance of study-specific clinical research regulatory binders.

  • Maintains requisite skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies.

  • Adheres to University and unit-level policies and procedures and safeguards University assets.

CORE QUALIFICATIONS:

Education:

Bachelor's degree in relevant field

Experience:

Minimum 1 year of relevant experience

Knowledge, Skills and Attitudes:

  • Skill in completing assignments accurately and with attention to detail.

  • Ability to analyze, organize and prioritize work under pressure while meeting deadlines.

  • Ability to process and handle confidential information with discretion.

  • Ability to work evenings, nights, and weekends as necessary.

  • Commitment to the University's core values.

  • Ability to work independently and/or in a collaborative environment.

Department Specific Functions

1. Assists in participant recruitment and retention activities and assists in screening potential study participants for eligibility.
2. Collects, processes, and ships specimens according to protocol and regulations.
3. Maintains study binders and filings according to protocol requirements, UM, and department policy.
4. Distribute study drug materials according to practice standards and clinical credentials as delegated by the Principal Investigator.
5. Assists in implementing protocol amendments under direct supervision of the Principal Investigator.
6. Assists with study orientation and protocol-related in-services to the research team and clinical staff.
7. Monitors protocol implementation and study progress; keeps investigators fully apprised of study progress; submits progress reports according to established schedule.
8. Learns the research team and assists with communications/interactions with sponsors, data coordinating centers, compliance monitors, collaborators, investigators' academic, administrative personnel, and departments.
9. Assists in administrative tasks of study personnel, including orientation, documenting core competencies, certification mandates, safety/responsible conduct of research education, and performance reviews.
10. Adheres to cultural competency guidelines; implements strategies to meet study participants' needs for language translation, health literacy, etc.
11. Follows the appropriate fundamental requirements of all international, national, and local regulatory bodies.

12. Local traveling to other sites might be required.

Department Specific Qualifications

Experience:

Bilingual in English and Spanish is preferred but not required.

The University of Miami offers competitive salaries and a comprehensive benefits package including medical, dental, tuition remission and more.

UHealth-University of Miami Health System, South Florida's only university-based health system, provides leading-edge patient care powered by the ground breaking research and medical education at the Miller School of Medicine. As an academic medical center, we are proud to serve South Florida, Latin America and the Caribbean. Our physicians represent more than 100 specialties and sub-specialties, and have more than one million patient encounters each year. Our tradition of excellence has earned worldwide recognition for outstanding teaching, research and patient care. We're the challenge you've been looking for.

The University of Miami is an Equal Opportunity Employer. Applicants and employees are protected from discrimination based on certain categories protected by Federal law.

Job Status:

Full time

Employee Type:

Staff

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About University of Miami

Sourced by ZipRecruiter

The University of Miami, located in the beautiful Coral Gables, Florida, is a comprehensive, private research institution in the United States. Operating within the higher education industry, the institution offers a multitude of degree programs spanning over 180 majors and program through its 12 colleges. The University was founded in 1925 with the mission to disseminate knowledge, transform lives, and change the world - a mission it has held faithfully to this day. Notably, the University of Miami has gained global recognition for its commitment to research and innovation, with over $324 million in research and sponsored project funding awarded annually.

Industry

Colleges, universities, and professional schools

Company size

10,000+ Employees

Headquarters location

Coral Gables, FL, US

Year founded

1925