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HealthcareISCO 3213

Clinical trial assistant

A clinical trial assistant is a person who supports clinical trials of medicines, working alongside researchers and doctors in hospitals.

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Rate 5 of the 10 essential skills of this occupation (European ESCO data). No account needed.

manage healthcare users' data

record data from biomedical tests

conduct health related research

apply good clinical practices

perform clinical coding procedures

About clinical trial assistant

The assistant manages the paperwork a trial cannot run without: case report forms, study protocols and informed consent forms, each of which has to be complete, signed, dated and traceable. The assistant keeps records of the side effects of medicines, noting each reported adverse effect. Clinical reports are prepared, and research data from biomedical studies is recorded as it is generated rather than reconstructed afterwards.

The assistant manages healthcare users' data and carries out clinical coding procedures so that findings can be counted and compared, and keeps treatment records in order.

Clinical sciences and medical studies give the assistant enough understanding to see when an entry does not fit the clinical picture, and the evidence-based approach of general medicine explains why a trial has to follow its protocol exactly for its results to be reliable. Entry routes include medical or related studies, and detailed requirements are set by the employer.

European Skills Framework

Skills and knowledge areas required for this occupation based on European classification.

Essential (10)

clinical reportsclinical reportsThe methods, assessment practices, credentials and opinions gathering procedures necessary for writing clinical reports.medical studiesmedical studiesThe basics and terminology of medical studies.clinical scienceclinical scienceThe research and development of the techniques and equipment used by medical staff to prevent, diagnose and treat illness.evidence-based approach in general practiceevidence-based approach in general practiceThe general principles, methods and concepts of scientific research and the fundamentals of statistics in medical care. The scientific background of pathology and theories about the forming of hypothe...manage healthcare users' datamanage healthcare users' dataKeep accurate client records which also satisfy legal and professional standards and ethical obligations in order to facilitate client management, ensuring that all clients' data (including verbal, wr...record data from biomedical testsrecord data from biomedical testsUse information technology to accurately record and analyse data from biomedical tests, writing reports on the data and sharing results with the appropriate persons.conduct health related researchconduct health related researchConduct research in health related topics and communicate findings orally, through public presentations or by writing reports and other publications.maintain treatment recordsmaintain treatment recordsKeep accurate records and file reports related to the prescribed treatment or medication.apply good clinical practicesapply good clinical practicesEnsure compliance with and application of the ethical and scientific quality standards used to conduct, record and report clinical trials that involve human participation, at an international level.perform clinical coding proceduresperform clinical coding proceduresMatch and record correctly the specific illnesses and treatments of a patient by using a clinical codes classification system.
Optional (4) — show
health records managementhealth records managementThe procedures and importance of record keeping in a healthcare system such as hospitals or clinics, the information systems used to keep and process records and how to achieve maximum accuracy of rec...patient record storagepatient record storageField of information which monitors regulatory and legal changes regarding patient record compilation and storage.clinical codingclinical codingThe matching of clinical statements with standard codes of illnesses and treatments through use of a classification system.record treated patient's informationrecord treated patient's informationRecord information accurately relating to the progress of the patient during therapy sessions.

Related Occupations

Occupations that need many of the same essential skills, so the move between them is shortest.

biomedical scientist4 shared essential skillsclinical informatics manager4 shared essential skillsmedical writer4 shared essential skillsspecialist biomedical scientist3 shared essential skillsadvanced physiotherapist2 shared essential skillsaudiologist2 shared essential skillsbiomedical scientist advanced2 shared essential skillsclinical coder2 shared essential skills

Frequently asked questions

What does a clinical trial assistant do?

Clinical trial assistants support clinical drug research. Collaborate with researchers and doctors in hospitals. Manage essential documents such as clinical case report forms, study protocols, and informed consent forms. File relevant logs related to side effects of medicines.

What skills does a clinical trial assistant need?

A clinical trial assistant needs 10 essential skills, including clinical reports, medical studies, clinical science, evidence-based approach in general practice, manage healthcare users' data.

Will AI replace clinical trial assistant jobs?

The AI disruption score for clinical trial assistant is 54/100 (moderate risk). Skills most exposed to automation: patient record storage, record data from biomedical tests, manage healthcare users' data. Most resilient: evidence-based approach in general practice, clinical science, conduct health related research.

Quick Facts

SectorHealthcare
ISCO GroupHealth associate professionals
Essential Skills10

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