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$49K

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How much do clinical research cro jobs pay per year?

As of Jun 25, 2026, the average yearly pay for clinical research cro in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What is the movie clinical about?

There is no widely known movie titled 'Clinical.' If you are referring to a specific film, please provide more details. As a Clinical Research Coordinator (CRC), understanding medical or research-related films can help in training or communication, but the job itself focuses on managing clinical trials and ensuring compliance with protocols.

What do we mean by clinical?

In the context of a Clinical Research Coordinator (CRC) role, 'clinical' refers to activities related to patient care, medical procedures, and the study of health conditions within a healthcare setting. It involves managing clinical trials, ensuring protocol compliance, and collecting data from human participants to evaluate new treatments or interventions.

What is a Clinical Research CRO?

A Clinical Research CRO, or Contract Research Organization, is a company that provides support to the pharmaceutical, biotechnology, and medical device industries by offering research services on a contract basis. These services can include clinical trial management, regulatory affairs, data management, pharmacovigilance, and biostatistics. CROs help sponsors conduct clinical trials more efficiently by leveraging their specialized expertise and resources, often leading to faster drug development timelines. They play a critical role in bringing new therapies to market by ensuring studies are conducted according to regulatory standards and scientific rigor.

What are some common challenges Clinical Research Associates (CRAs) face when working with multiple clinical trial sites?

Clinical Research Associates often juggle responsibilities across several trial sites, which can present challenges such as coordinating schedules, ensuring consistent protocol adherence, and managing site-specific documentation. Effective communication is crucial, as CRAs must regularly interact with site staff, investigators, and sponsors to resolve issues and maintain regulatory compliance. Adapting to different site cultures and workflows while meeting tight timelines requires strong organizational skills and flexibility. These challenges are balanced by the dynamic nature of the role, offering frequent learning opportunities and professional growth.

What are the key skills and qualifications needed to thrive as a Clinical Research CRO, and why are they important?

To thrive in a Clinical Research CRO (Contract Research Organization), you need a solid background in life sciences or pharmacy, experience in clinical trial management, and knowledge of regulatory guidelines like GCP. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and relevant certifications such as ACRP or SOCRA are typically required. Strong organizational skills, attention to detail, and effective communication are essential soft skills for coordinating studies and collaborating with diverse stakeholders. These skills and qualifications are crucial to ensuring compliance, accurate data collection, and the successful execution of clinical trials.

What does it mean for someone to be clinical?

In the context of a Clinical Research CRO, being clinical refers to working directly with human subjects in medical studies or trials to evaluate the safety and effectiveness of new treatments or drugs. It involves understanding clinical protocols, adhering to regulatory standards, and often requires knowledge of medical terminology and data collection tools.

What does very clinical mean?

In the context of a Clinical Research Coordinator (CRC) role, 'very clinical' typically refers to a work environment that involves direct interaction with patients, detailed understanding of medical procedures, and adherence to clinical protocols. It indicates a focus on clinical aspects such as patient safety, data accuracy, and compliance with regulatory standards, often requiring knowledge of medical terminology and clinical trial processes.
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Clinical Research Cro jobs near you
Infographic showing various Clinical Research Cro job openings in the United States as of June 2026, with employment types broken down into 80% Full Time, and 20% Part Time. Highlights an 72% Physical, 3% Hybrid, and 25% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Coordinator Clinical Research

McLaren Health Care Corporation

Flint, MI • On-site

$23.50 - $31.25/hr

Full-time

Posted 6 days ago

McLaren Health Care rating

6.7

Company rating: 6.7 out of 10

Based on 210 frontline employees who took The Breakroom Quiz

522nd of 875 rated healthcare providers

Job description

Position Summary:
Responsible for facilitating research studies; providing knowledgeable information regarding each research protocol to the medical and nursing staff; evaluating the eligibility of potential candidates for research studies; assisting in the informed consent process; monitoring research study compliance; collecting and submitting data; coordinating required study procedures to meet protocol requirements and maintain a system for effective data flow.
Essential Functions and Responsibilities:
1. Evaluates eligibility of candidates for clinical research studies by reviewing protocol defined eligibility requirements and/or collecting pertinent data on potential candidates, verifying appropriateness of patients for entry to clinical trials, and assisting the other staff in determining eligibility of potential patients.
2. Assists the investigator with the informed consent process and assures that the research team and the patient have adequate information to achieve the informed consent process.
3. Registers and randomizes eligible patients.
4. Submits accurately completed data collection forms to the sponsor or CRO in a timely manner as dictated by the study protocol.
5. Coordinates tests and procedures as specified in the study protocol through accurate communication with the site / principal investigator, physicians, patients, nurses, and office/hospital staff.
6. Maintains contact with regulatory specialist to ensure data submitted to the IRB of record is accurate and timely. Upon request, submits regulatory documents to regulatory specialist to include in the IRB submission or submission to sponsor or CRO.
7. Assists the investigators and clinicians in identifying and enrolling eligible patients into clinical trials/ studies and assures compliance to protocol requirements.
8. Educates patients and their families regarding research protocols and keeps them informed of procedures and changes in the studies in which they are participating.
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Qualifications:
Required:
  • High School Diploma or equivalent
  • Two years' experience in clinical research or five-years in a health care role (ex. paramedic, emergency medical technician, radiology technician)

Preferred:
  • Degree in biology, psychology, or other clinical research -related area or equivalent education and experience
  • Three or more years of experience in clinical research
  • Clinical research certification through SOCRA or ACRP

Equal Opportunity Employer of Minorities/Females/Disabled/Veterans

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