What Does a Clinical Research Consultant Do?

Clinical research consultants oversee all processes and results of clinical trials. Additionally, they ensure all research meets with regulations set by employers or sponsors and is conducted according to these.

Find CRA jobs in pharmaceutical, medical device, and contract research organizations (CRO). Ensure to read each job description closely and highlight your abilities in your CV.

Job description

Clinical research consultant perform various roles within their field. Depending on their level of experience, clinical research consultants may serve as trial process managers, people managers, or project managers; responsible for implementing study tools, documenting data collection procedures, monitoring budget allocations and providing strategic input in trials – not forgetting training staff members!

Clinical research consultants not only analyze data and present reports; they often interact directly with patients as well. For instance, they might explain any procedures they’re about to undergo or ease any anxiety they might have about undergoing it. Furthermore, clinical research consultants often assist sales staff with new software demonstrations as well as participate in focus groups or design teams.

Every pill, vaccine and medical device that you could take to enhance your health must pass a series of clinical research trials monitored by a clinical research associate (CRA). A CRA acts as the link between those sponsoring the research and clinics facilitating its implementation.

Education requirements

Clinical trials are essential in ensuring that drugs, vaccines, procedures and medical devices that improve or prevent illness go through rigorous scrutiny before being approved for use. Clinical research associates (CRAs) play an integral part of this process by acting as liaisons between those conducting trials and sponsors who fund them.

Employers typically require candidates for CRA positions to possess at least an undergraduate degree. Some employers may accept postgraduate qualifications, though this isn’t necessary.

CRAs must possess strong organizational and time management skills as well as be capable of meeting tight deadlines. Travel between trial sites may necessitate long hours at times. Depending on the nature of their work, a CRA may either work full time for one company or freelance for several clients; depending on their profession type they could find employment with hospitals, pharmaceutical companies or CROs as in-house consultants or freelance consultants; recruitment agencies often offer such positions too.


Every medication, vaccine, therapy or medical device that improves your health undergoes clinical research trials to help doctors and researchers ascertain its safety and efficacy for consumers. Clinical Research Associates (CRAs) are an integral part of this process – working full-time shifts to collect, analyze and report data to their company or institution of employment and present their findings accordingly.

Pharmaceutical and medical device companies as well as contract research organisations frequently hire clinical research assistants (CRAs). CRAs may be involved in all phases of clinical trials from selecting sites through monitoring and closing down studies, to working on post-launch trials that assess drug safety.

Careers as Clinical Research Associates can be rewarding, yet require substantial education and experience for certification. Many CRAs begin in entry-level roles such as administrative assistant or data coordinator to gain this experience.

Work environment

Each pill, vaccine, procedure or medical device used to enhance health undergoes clinical research trials prior to being released for public consumption. These trials are overseen by clinical research associates (CRA). They serve as intermediaries between those sponsoring research and those who facilitate clinical trials.

Clinical research consultants spend much of their time visiting medical professionals at trial centers, healthcare practices and hospitals as well as attending conferences and training courses. Some companies may allow for remote working opportunities depending on which consultant is hired.

Clinical research consulting companies seek candidates with strong analytical abilities and in-depth knowledge of clinical research. Experience with data processing and IT systems are also necessary; candidates must also possess teamwork capabilities, as well as be capable of communicating effectively within teams. Furthermore, candidates must possess an in-depth knowledge of both the trial process and any applicable regulatory guidelines for this job.