Clinical research associates are also referred to as CRAs. They are responsible for organizing and administering clinical trials of a current or new drug to assess and determine the risks and the benefits associated with using them. Clinical research associates are often employed by clinical contract agencies and pharmaceutical companies. There are many things that a clinical research associate needs to handle, and we will discuss them in this article.

Their responsibilities

The key responsibilities that a clinical research associate has to carry out in their course of duty include:

 Writing reports

 Progress monitoring during the trial duration

 Collection and authentication of forms that are used for data collection

 Giving the clinicians instructions about how trials are to be conducted

 Designing different trial materials as well as providing different study centers that have sufficient quantities

 Setting up the trial centers and then disbanding them

 Identifying the clinicians and briefing them

 Writing down the procedures of the drug trials

The employers

Typical employers include:

 The academic departments in hospitals

 Clinical contract houses and agencies (CROs)

 Pharmaceutical companies

Available vacancies are usually advertised in the national newspapers, online, specialist agencies, and very specific journals. This field is very competitive, therefore it can be useful for applicants to have the relevant analytical and scientific techniques. In addition, pharmaceutical research, medical sales, nursing, or laboratory work knowledge can be very useful in clinical research associate positions.

The process of recruitment involves an interview, which is very technical. You will need to be trained to get the kind of qualifications that are necessary to excel in this area. To achieve this, you need to be qualified in life sciences or medical sciences. To learn more about clinical research professional courses, visit CCRPS.

Unveiling the Role of Clinical Research Associates

Clinical Research Coordinator: Dive into the responsibilities and skills required for effective clinical research coordination.

1. Pharmacovigilance Certification: Explore the essential aspects of pharmacovigilance to ensure drug safety and regulatory compliance.

2. CRA (Clinical Research Associate): Delve into the core responsibilities and duties of a Clinical Research Associate in managing clinical trials.

3. ICH-GCP: Understand the principles and guidelines outlined by the International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH) Good Clinical Practice (GCP).

4. Clinical Trials Assistant Training: Acquire the foundational knowledge and skills necessary to support clinical trial operations effectively.

5. Advanced Clinical Research Project Manager Certification: Elevate your expertise in clinical research project management with advanced certification training.

6. Advanced Principal Investigator Physician Certification: Gain advanced certification tailored for Principal Investigator Physicians involved in clinical research studies.

7. Medical Monitor Certification: Explore the critical role of medical monitoring in ensuring the safety and integrity of clinical trials.