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Clinical Research Coordinator Work From Home jobs

Senior clinical trial manager.

Unblinded Clinical Trial Manager (Remote)

Tandym Group

Clinical Trial Manager - Boston (Remote)

Clinical research operations specialist ii (react), charge capture coordinator - clinical revenue integrity - full time 8 hour days remote (non-exempt) (non-union), onsite study coordinator (part-time, contractor).

Wireless Generation

Clinical Research Senior Medical Scientist, Cardiovascular

Study coordinator, clinical research associate (veterinary), part-time clinical science professional (entry - intermediate level) (0.5 fte), clinical research associate - physical therapist experience, field clinical research associate (remote), principal clinical research associate, remote women's fertility clinical research associate iii.

Global Channel Management, Inc.

Clinical Research Associate - Remote

Caldera Medical

Senior Clinical Research Coordinator (CRC III)

Headlands Research

Senior Clinical Research Specialist - National

Research advocacy coordinator, clinical research coordinator.

Mass General Brigham

Clinical Research Coordinator I (Hybrid) - Psychiatry

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The Career Path of a Clinical Research Coordinator

Learn about the clinical research coordinator role, sometimes called a clinical trials manager. Discover pathways to work in clinical research, salaries, and typical employers.

A clinical research coordinator is an integral part of the research team for medical studies. They conduct and manage clinical trials, providing outcomes that shape medical advances in preventative care, curing diseases, and immunizations, among other areas. With employment options available in hospitals, pharmaceutical companies, and private companies, clinical research coordinators can seek various positions, and salary is above average compared to similar professions.

What is a clinical research coordinator?

A clinical research coordinator—sometimes known as a clinical trial manager—supervises clinical research and drug trials, such as interventions involving drugs, devices, or procedures promoting behavior changes. In this position, you would recruit and screen participants, coordinate the day-to-day running of the trials, collect data, and produce reports. 

A clinical research coordinator is also responsible for ensuring a trial's safety and keeping the materials used safe during and after the study. You ensure meeting certain regulations and ethical standards and track patient health and progress. 

Where does a clinical research coordinator sit in a clinical research team?

A clinical research coordinator reports to a principal investigator, who is responsible for the overall design and management of the study. In contrast, a clinical researcher organizes the day-to-day running of the trials. As a clinical research coordinator, you will also work closely with sponsors and staff within their department responsible for finance, personnel, and compliance. You will typically oversee a clinical research team, including doctors, nurses, other medical staff, and assistants.

What are the primary duties and responsibilities of a clinical research coordinator?

Clinical research coordinators work in various workplaces, from hospitals to private businesses, and your duties will vary according to where you work and what you are trialing. However, typical responsibilities include:

Coordinating and overseeing the running of clinical trials

Recruiting and screening participants for trials

Managing documents and records of participants and trials 

Ensuring trials are delivered following regulatory, government, and ethical regulations and requirements

Ensuring the safety of participants, supplies, and materials

Performing cost analysis and preparing budgets

Designing and delivering training to staff and participants 

Collecting data and maintaining detailed records

Acting as a point of contact for study participants to ask any questions or express concerns 

Promoting the study through meetings, events, and seminars

Overseeing the research team

Career pathway steps

To work in clinical research, you need to hold a degree and have a certain amount of experience. You can pursue certifications and graduate qualifications to further your chances of a position. 

Bachelor's degree

A bachelor’s degree is generally step one for anyone who wants to work as a clinical research coordinator. A Bachelor of Science in a relevant subject, such as clinical research administration or a matter under the umbrella of health sciences, public health, or microbiology, is recommended. 

Read more: Bachelor of Science (BS) Degree: What It Is and How to Earn One

Work experience

Experience in health care or clinical research is essential for most positions. Some professionals come from a background in nursing or health care. If you have limited experience, getting some through an internship, voluntary assignment, or an entry-level role in a hospital or research position is a good idea. Experience is essential to be able to work towards certain industry-specific certifications.

Master's degree or graduate certificate 

All you need to work as a clinical research coordinator is a bachelor’s degree and experience. However, some employers prefer a graduate degree, and having a graduate certificate or a master’s degree will help set you apart from other applicants without this education level. 

You have several options to consider, and there is no set course. Still, it is most advantageous to select a subject like clinical research, clinical administration, or clinical research management to combine the elements of clinical research and a level of leadership. Specializations like medical technology are also options, as are more general course subjects like life sciences or health sciences. 

When choosing a course, essential factors to consider are whether there is a good mix of theory and practical experience and whether the course covers clinical and managerial subjects to give you a broad range of expertise. If you are already working and gaining experience, consider the flexibility of studying part-time or online to achieve your educational goals.

In addition to a master’s degree, you can also study for a graduate certificate in a relevant subject. These courses tend to be part of the curriculum for a master’s degree, and you can transfer credits, so it’s a great way to gain a certificate while building towards a master’s degree.

Read more: How to Get a Master's Degree

Certification

It isn’t essential but recommended that you get a clinical research certification if you want to advance your career in clinical research. To become certified, you need to be working in the field. Certification verifies your skills and competence, potentially boosting career prospects and salary. The Association of Clinical Research Professionals (ACRP-CP) provides a variety of certifications for clinical research professionals:

ACRP Certified Professional (ACRP-CP): To validate your knowledge and skills as a clinical research professional

Clinical Research Coordinator (CCRC): To validate your knowledge and skills as a clinical research coordinator

Clinical Research Associate (CCRA): To validate your knowledge and skills as a clinical research associate

Principal Investigator (CPI): To validate your knowledge and skills as a principal investigator

ACRP Medical Device Professional Subspecialty (ACRP-MDP): To validate your knowledge of medical device trials

ACRP Project Manager Subspecialty: To validate your knowledge of project management within clinical research

The Society of Clinical Research Associates (SOCRA) also provides its Certified Clinical Research Professional credential to validate your experience, education, and knowledge as a clinical research professional.

How much do clinical research coordinators get paid?

The average clinical research coordinator's salary is $56,504, according to Glassdoor [ 1 ]. This can reach over $89,000 [ 1 ] for more senior positions. Salaries vary according to employer, industry, and type of trial. 

Who are typical employers of clinical research coordinators?

A clinical research coordinator can work in various places, including health care organizations, pharmaceutical companies, research hospitals, and government and private companies. You may be employed to research new medicines for market, genetic diseases, illness prevention, and behavioral prevention. 

If you’re ready to take your next steps towards a career as a clinical research coordinator, you can start with a short course on Design and Interpretation of Clinical Trials delivered by John Hopkins University on Coursera. This can give you a good grounding in understanding clinical trials and research.

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Article sources

Glassdoor. “ Clinical Research Coordinator Salaries , https://www.glassdoor.com/Salaries/us-clinical-research-coordinator-salary-SRCH_IL.0,2_IN1_KO3,32.htm.” Accessed March 9, 2023.

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Coursera’s editorial team is comprised of highly experienced professional editors, writers, and fact...

This content has been made available for informational purposes only. Learners are advised to conduct additional research to ensure that courses and other credentials pursued meet their personal, professional, and financial goals.

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What does a clinical research coordinator do?

Would you make a good clinical research coordinator? Take our career test and find your match with over 800 careers.

What is a Clinical Research Coordinator?

A clinical research coordinator (CRC) plays an important role in the field of clinical research, ensuring the smooth and efficient conduct of clinical trials and studies. These professionals act as a bridge between the research investigators, sponsors, and participants, overseeing various aspects of the research process. They collaborate closely with physicians, nurses, and other healthcare professionals to guarantee the well-being of study participants while collecting valuable data that contributes to scientific advancements and the development of new treatments and therapies.

To excel as a clinical research coordinator, individuals typically need a strong background in life sciences, healthcare, or a related field. Attention to detail, excellent organizational skills, and the ability to communicate effectively are essential.

What does a Clinical Research Coordinator do?

Duties and Responsibilities Clinical research coordinators have a wide array of duties and responsibilities aimed at ensuring the successful implementation and completion of clinical trials. Their roles are multifaceted and demanding, requiring a combination of organizational, interpersonal, and scientific skills. Some key duties and responsibilities include:

• Protocol Management: CRCs are responsible for understanding and implementing the research protocol thoroughly. They ensure that all aspects of the study adhere to the protocol, including participant eligibility criteria, investigational product administration, and data collection procedures.
• Participant Recruitment and Informed Consent: CRCs actively recruit eligible participants for the clinical trial. They explain the study details, benefits, and risks to potential participants and obtain their informed consent to participate in the research.
• Data Collection and Management: CRCs collect accurate and comprehensive data from participants during the study, maintaining detailed records. They may use electronic data capture systems to ensure data accuracy and integrity.
• Clinical Procedures: Depending on their qualifications and the nature of the study, CRCs might perform certain clinical procedures such as drawing blood, taking vital signs, or administering investigational drugs under the supervision of a licensed healthcare provider.
• Regulatory Compliance: CRCs ensure that the study complies with all relevant regulations, including guidelines set by the Food and Drug Administration (FDA) and the Institutional Review Board (IRB). They assist in preparing and submitting regulatory documents for study approval and conduct regular audits to maintain compliance.
• Safety Monitoring: CRCs monitor participants for adverse events and ensure appropriate and timely reporting of these events to regulatory authorities and sponsors.
• Collaboration: CRCs work closely with principal investigators, research nurses, pharmacists, and other healthcare professionals involved in the study. They facilitate effective communication among team members to ensure the smooth progress of the research.
• Administrative Tasks: CRCs are often responsible for managing the administrative aspects of the study, including scheduling participant visits, organizing meetings, and maintaining study-related documentation.
• Quality Control: CRCs perform quality control checks to ensure that the collected data is accurate, complete, and in compliance with the study protocol. They also participate in monitoring visits conducted by sponsors or regulatory agencies.
• Education and Support: CRCs provide education and support to study participants, addressing their concerns and questions throughout the trial. They serve as a primary point of contact between participants and the research team.

Types of Clinical Research Coordinators Clinical research coordinators can specialize in various areas within the field of clinical research, each requiring specific skills and expertise. Here are some common types of CRCs based on their specialized roles:

• Clinical Research Nurse Coordinator: These CRCs are registered nurses (RNs) with specialized training in clinical research. They often have a strong background in patient care and are responsible for both the clinical and research aspects of the studies. Clinical Research Nurse Coordinators may administer medications, perform clinical procedures, and monitor participants' health throughout the trials.
• Regulatory Affairs Coordinator: Regulatory CRCs focus on ensuring that the clinical trials comply with all applicable regulations and guidelines. They prepare and submit documents for regulatory approval, liaise with regulatory authorities, and keep the research team informed about any changes in regulations that might affect the study.
• Data Coordinator: Data CRCs are responsible for collecting, managing, and analyzing the data generated during clinical trials. They ensure data accuracy, integrity, and confidentiality. These professionals often work closely with statistical teams and use various software tools for data analysis.
• Recruitment Coordinator: Recruitment CRCs specialize in participant recruitment and retention. They develop strategies to identify eligible participants, engage with potential candidates, explain the study details, and address concerns. Their role is crucial in ensuring that studies meet their enrollment goals.
• Pediatric Clinical Research Coordinator: Specializing in pediatric clinical trials, these CRCs have expertise in working with children and adolescents. They understand the unique ethical and logistical challenges associated with pediatric research and ensure that the trials are conducted safely and ethically in younger populations.
• Oncology Research Coordinator: Oncology CRCs work specifically on cancer-related clinical trials. They collaborate with oncologists and other specialists to coordinate complex cancer studies, which often involve novel therapies and treatments.
• Quality Assurance Coordinator: Quality Assurance CRCs focus on ensuring that the clinical trial processes and data collection adhere to quality standards and protocols. They conduct internal audits, develop quality control procedures, and assist in preparing for external audits from regulatory authorities or sponsors.
• Site Management Coordinator: Site Management CRCs oversee the operations of clinical trial sites. They coordinate activities among various research sites, ensuring consistency in protocol implementation, data collection, and reporting. Site Management CRCs also facilitate communication between different sites and the central research team.

Are you suited to be a clinical research coordinator?

Clinical research coordinators have distinct personalities . They tend to be investigative individuals, which means they’re intellectual, introspective, and inquisitive. They are curious, methodical, rational, analytical, and logical. Some of them are also enterprising, meaning they’re adventurous, ambitious, assertive, extroverted, energetic, enthusiastic, confident, and optimistic.

Does this sound like you? Take our free career test to find out if clinical research coordinator is one of your top career matches.

What is the workplace of a Clinical Research Coordinator like?

Clinical research coordinators work in a variety of settings, primarily in environments related to healthcare, research, and pharmaceutical industries. Here are the typical workplaces for CRCs:

Academic Medical Centers: Many CRCs are employed at universities and academic medical centers, where they collaborate with researchers, physicians, and other healthcare professionals to conduct clinical trials. These settings often involve a combination of patient care and research activities.

Hospitals: Hospitals, especially those with research-focused departments, employ CRCs to coordinate and manage clinical trials. In hospital settings, CRCs work closely with medical staff and patients, often in specialized departments like oncology, cardiology, or neurology.

Clinical Research Organizations (CROs): CROs are specialized companies hired by pharmaceutical, biotechnology, and medical device companies to conduct clinical trials on their behalf. CRCs in CROs manage multiple clinical trials across different therapeutic areas and work with various sponsors and research sites.

Pharmaceutical and Biotechnology Companies: CRCs can work directly for pharmaceutical and biotechnology companies, overseeing in-house clinical trials to test new drugs, treatments, or medical devices. In this setting, CRCs collaborate closely with scientists, regulatory affairs professionals, and project managers.

Government and Nonprofit Organizations: Some CRCs are employed by government agencies (such as the National Institutes of Health) and nonprofit organizations (such as research foundations or advocacy groups) that fund and conduct clinical research. These professionals are involved in a wide range of studies aimed at advancing scientific knowledge and public health.

Private Research Clinics: Private research clinics specialize in conducting clinical trials. CRCs in these settings work on a variety of studies and often have a more streamlined and focused work environment compared to larger medical institutions.

Home-based Work: With advancements in technology, some CRCs may have the flexibility to work remotely for certain tasks, such as data analysis, regulatory document preparation, or administrative tasks. However, a significant portion of their work still involves on-site activities, especially those related to direct participant interaction and clinical procedures.

Clinical Research Coordinators are also known as: CRC