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Clinical Research Cro Jobs (NOW HIRING)

McLaren

Coordinator Clinical Research

Flint, MI · On-site

$23.50 - $31.25/hr

... for clinical research studies by reviewing protocol defined eligibility requirements and/or ... CRO in a timely manner as dictated by the study protocol. 5. Coordinates tests and procedures as ...

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$49K

$107.3K

$189K

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.

Clinical Research Nurse

Prolerity Clinical Research

Marrero, LA • On-site

Full-time

Posted 23 days ago

Job description

Description:

The Clinical Research Nurse oversees the daily activities of clinical research studies. They

work closely with the clinical teams and investigators to ensure that all required

procedures and visits occur according to protocol specific guidelines.

RESPONSIBILITIES

  • Understand thoroughly all assigned studies through reading protocols, attending investigator meetings and start-up meetings, and coordinating with Principal Investigator
  • Adhere strictly to the study protocol; obtain exemptions when necessary/appropriate
  • Communicate protocol issues to CRO and/or Sponsor, Site Administrator, Director, Principal or Sub-Investigator
  • Articulate all pertinent issues to the PI or document by email/letter or during meetings
  • Collect initial psychiatric and medical information by interviewing patients and by accessing other appropriate sources
  • Ensure a flow of communication including telephone conferences between patient, study staff, referral sources, Sponsor and/or CRO, Monitor(s), Auditors and any marketing groups hired by the Sponsor
  • Utilize various rating scales and maintain interrater reliability with other clinicians
  • Perform clinical tasks including, but not limited to, vital signs, height and weight, ECG, phlebotomy, specimen packaging
  • Maintain timely source documentation as well as sponsor required information.
  • Dispense and maintain accurate records of study medication
  • Educate patients and family regarding their particular study and clinical drug trials in general.
  • Complete all monitor and sponsor queries in a timely manner
  • Provide appropriate community resource referrals to patients, caretakers, and family at conclusion of patient’s participation in study
Requirements:
  • Ability to communicate clearly and effectively (written and verbal)
  • Ability to communicate in an active multi-office environment
  • Must possess excellent interpersonal and customer service skills
  • Ability to multi-task, organize, prioritize appropriately, and work well both individually and as part of a team
  • Ability to use time productively and contribute to high levels of company operational efficiency and effectiveness
  • Ability to maintain confidentiality of information
  • Ability to efficiently operate all job-related office equipment (telephone, computer, calculator, fax, copier, study-specific equipment)

Required Experience

  • Bachelor’s degree required
  • RN licensure
  • Experience as a Clinical Research Coordinator (CRC) or Research Assistant