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Temporary Weekend Clinical Research Jobs (NOW HIRING)

The University of Miami

Clinical Research Coordinator 1

Miami, FL · On-site

$23.25 - $30.75/hr

  • Medical

  • Dental

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 ...

University of Miami

Clinical Research Coordinator 1

Miami, FL · On-site

$23.25 - $30.75/hr

  • Medical

  • Dental

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 ...

University of Miami

Clinical Research Coordinator 1

Miami, FL

$23.25 - $30.75/hr

  • Medical

  • Dental

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 ...

TriHealth

Clinical Research Manager

Montgomery, OH · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

The Clinical Research Manager plays a pivotal role at the intersection of patient care, research ... No Weekend or Holiday Commitment Benefits: TriHealth offers a comprehensive benefits package which ...

The University of Miami

Clinical Research Coordinator 1

Miami, FL · On-site

$23.25 - $30.75/hr

  • Medical

  • Dental

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 ...

The University of Miami

Clinical Research Coordinator 1

Miami, FL · On-site

$23.25 - $30.75/hr

  • Medical

  • Dental

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 ...

TriHealth, Inc.

Clinical Research Site Manager

Montgomery, OH · On-site

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

The Clinical Research Site Manager plays a pivotal role at the intersection of patient care ... No Weekend or Holiday Commitment Benefits: TriHealth offers a comprehensive benefits package which ...

The University of Miami

Clinical Research Coordinator 1

Miami, FL · On-site

$23.25 - $30.75/hr

  • Medical

  • Dental

If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click ... Adapt to flexible working hours, including evenings, nights, and weekends, as necessary to support ...

Guidehouse

Clinical Research Coordinator

Bethesda, MD · On-site

$65K - $108K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Provide guidance and operational training to junior staff, trainees, students, and temporary personnel as requested by the Government. * Coordinate multiple clinical research studies simultaneously ...

The University of Miami

Clinical Research Coordinator 1

Miami, FL · On-site

$23.25 - $30.75/hr

  • Medical

  • Dental

If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click ... Adapt to flexible working hours, including evenings, nights, and weekends, as necessary to support ...

University of Miami

Clinical Research Coordinator 1

Miami, FL · On-site

$23.25 - $30.75/hr

  • Medical

  • Dental

If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click ... Adapt to flexible working hours, including evenings, nights, and weekends, as necessary to support ...

Actalent

Clinical Research Nurse

Mobile, AL · On-site

$35 - $42/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Job Title: Clinical Research Nurse (Oncology) - Part-Time, Mobile, AL This part-time Clinical ... If eligible, the benefits available for this temporary role may include the following: - Medical ...

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Temporary Weekend Clinical Research information

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

As of Aug 15, 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:

Temporary Weekend Clinical Research jobs near you

Clinical Research Specialist I - Oncology & Clinical Research

Cedars Sinai

Los Angeles, CA • On-site

$31.75 - $53.98/hr

Full-time

Posted 10 days ago

Cedars-Sinai rating

8.6

Company rating: 8.6 out of 10

Based on 131 frontline employees who took The Breakroom Quiz

41st of 1,059 rated hospitals

Job description


Location: Los Angeles, CA (Onsite)
This position is 100% onsite during the training period. After successful completion of training and demonstrated proficiency, there may be the opportunity for a limited hybrid work schedule based on business needs and performance. Candidates should be prepared to work onsite full-time initially.
Make an Impact on Groundbreaking Cancer Research: Are you passionate about advancing clinical research that directly impacts patient care? We are seeking a highly organized, detail-oriented Clinical Research Specialist I to support innovative oncology research initiatives and clinical trials. In this role, you will provide critical research infrastructure support while partnering with investigators, research teams, and laboratory personnel to ensure high-quality study execution, regulatory compliance, and exceptional data integrity.
This is an excellent opportunity for an experienced clinical research professional who thrives in a fast-paced environment, enjoys managing multiple priorities, and is committed to advancing translational and clinical research.
What You'll Do
As a Clinical Research Specialist I, you will play a key role in supporting departmental and institutional research initiatives by:
Clinical Research Operations
  • Participate in the design, implementation, and coordination of clinical research projects.
  • Support investigator-initiated research, including protocol development, case report forms, study documentation, budgets, and research committee coordination.
  • Coordinate research activities across departments while communicating project status and improvement opportunities to leadership.
  • Support research quality management initiatives and clinical trial recruitment efforts.

Molecular Twin & Oncology Research Support
  • Screen patients for protocol eligibility.
  • Coordinate participant blood collection activities according to study protocols.
  • Prepare Research Lab Kits (RLKs) and monitor participant visits.
  • Create participant cohorts and generate customized reports for investigators.
  • Develop and maintain oncology-focused research databases.
  • Maintain study forms, Standard Operating Procedures (SOPs), and research documentation.

Laboratory & Sample Management
  • Prepare research kits for multiple clinical protocols.
  • Process, prepare, store, distribute, and ship biological specimens according to protocol requirements.
  • Support pharmacokinetic (PK) collections, including occasional late-day or weekend sample processing as required by study timelines.
  • Ensure accurate tracking and reconciliation of biological samples across multiple databases.

Data Quality & Process Improvement
  • Perform quality control (QC) reviews of patient and sample data.
  • Enter and reconcile research information across multiple systems.
  • Identify opportunities to improve workflows, automate manual processes, and reduce data entry errors.

Regulatory Compliance
  • Ensure compliance with FDA regulations, IRB requirements, HIPAA, Good Clinical Practice (GCP), and all institutional research policies.
  • Participate in required training and continuing education.

Qualifications
To be considered, candidates must meet all of the following 2 requirements:
  1. Bachelor's degree in a scientific, healthcare, or related discipline.
  2. Minimum of three (3) years of clinical research experience within an academic medical center, hospital, research institution, biotechnology, pharmaceutical, or related clinical research environment.

Licenses and Certifications
  • Clinical Research AssociateACRP/SoCRA (or equivalent) certification preferred.

The ideal candidate has at least 3 years of clinical research experience, including coordinating clinical research studies and supporting research operations. You should have experience working with biological specimens (collection, processing, storage, or shipment), be familiar with Good Clinical Practice (GCP) and clinical research regulations, and have strong organizational skills with the ability to manage multiple priorities. Success in this role also requires exceptional attention to detail, experience with research databases and electronic data management systems, and the ability to communicate and collaborate effectively across multidisciplinary teams.
You'll stand out if you also have experience in oncology research, biobanking, or molecular research initiatives, along with exposure to protocol development, investigator-initiated studies, laboratory operations supporting clinical trials, reporting, database management, or process improvement and automation initiatives. An ACRP, SoCRA, or equivalent Clinical Research certification is preferred but not required.

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