Clinical Research Coordinator

Work environment

Clinical Research Coordinators typically work in hospitals, medical research centers, universities, or pharmaceutical companies. The role may involve office work, direct interaction with research participants, and collaboration with medical professionals and regulatory bodies.

Quick task list

• Coordinates and oversees the day-to-day operations of clinical trials.
• Ensures compliance with regulatory requirements and ethical standards.
• Recruits, screens, and collects informed consent from research participants.
• Maintains accurate records and manages data collection.
• Communicates with the research team, sponsors, and regulatory bodies.

Description

Clinical Research Coordinators are essential in bridging the gap between the theoretical design of clinical trials and their practical implementation. They require a thorough understanding of medical terminology, clinical research procedures, and regulatory guidelines, such as those from the FDA or IRB (Institutional Review Board). Their role involves meticulous attention to detail in documenting the trial process, ensuring the integrity and reliability of data collected.

The position demands strong organizational skills to manage the various components of a clinical trial, including participant recruitment and scheduling, regulatory compliance, and resource allocation. Coordinators also need excellent interpersonal skills to interact with participants, addressing their questions and concerns, and ensuring their safety and well-being throughout the study.

Clinical Research Coordinators must be adaptable and capable of problem-solving, often needing to adjust trial parameters or procedures in response to unforeseen challenges. They also play a vital role in interpreting and communicating trial results, collaborating with principal investigators and sponsors to translate findings into meaningful outcomes.

Typical education

A bachelor's degree in a health science, nursing, or related field is generally required, with some positions preferring or requiring a master's degree. Additional certification in clinical research coordination is beneficial.

High school preparation

Courses:

• Science courses (biology, chemistry, and physics) to build a foundation in life sciences.
• Mathematics for data analysis and statistics.
• Health sciences or anatomy classes for medical knowledge.
• Communication and English for report writing and effective communication.

Extra-Curricular Activities:

• Volunteering in healthcare settings, like hospitals or clinics.
• Participating in science clubs or fairs.
• Internships or shadowing opportunities in medical or research facilities.

Preparation after high school

Courses:

• Bachelor's degree in a health-related field.
• Courses in clinical research, biostatistics, and medical ethics.
• Master's degree in clinical research, public health, or a related field for advanced positions.

Experiences:

• Internships or entry-level positions in clinical research settings.
• Certification programs in clinical research coordination.

More resources

• Association of Clinical Research Professionals (ACRP) - Provides certification, training, and career development resources for clinical research professionals.
• Occupational Information Network (O*NET Online) - Offers comprehensive career information for Clinical Research Coordinators, including job duties and skills required.
• Society of Clinical Research Associates (SoCRA) - A global, non-profit organization that offers certification and education for clinical research professionals.
• Clinical Trials.gov - A database of privately and publicly funded clinical studies conducted around the world, useful for understanding the scope and variety of clinical research.
• National Institutes of Health (NIH) - Office of Clinical Research - Provides resources and training opportunities for those involved in clinical research.

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