£1,500

Clinical Research Associates (CRA) Beginners Course

Actions and Detail Panel

£1,500

Event Information

Share this event

Date and time

Location

Location

Citadines Holborn

94-99 High Holborn

London

WC1V 6LF

United Kingdom

View Map

Refund policy

Refund policy

No Refunds

Event description
CPD ACCREDITED, CLINICAL RESEARCH ASSOCIATE (CRA) BEGINNERS COURSE. Classroom, Instructor Led, Based Training!

About this event

CLINICAL RESEARCH ASSOCIATE (CRA)

Are you a CTA looking to advance to a CRA level? Are you a CRA with limited experience seeking training to improve your skills and performance? Are you a Research Nurse or Data Manager who has landed your first CRA role? If so, this Clinical Research Associate course provided by CGX Training is an excellent starter course that can equip you with the skills to conduct clinical trial initiation and or/ monitoring and basic site management at the investigational site.

A CPD accredited 3-day intensive course which provides those starting or looking to improve their skills as a CRA with a comprehensive and valuable insight into the entry-level role of a Clinical Research Associate (CRA). 

A clinical Research Associate (CRA) primarily manages the managerial aspects of a number of clinical trials, at every stage of the process.

This is fundamentally a “practical” and “hands on” workshop that focuses on current practice to ensure the CRA delegate develops practical experience of the role. Participants will learn about the role and responsibilities of the clinical research associate in the context of the regulations and rules that govern clinical trials.

TOPICS

  • ICH- GCP
  • The primary duties of a CRA
  • The specific responsibilities in accordance with ICH-GCP, SOP and regulations:
  • Before the clinical phase of the trial commences
  • During the clinical conduct of the trial
  • After completion or termination of the trial
  • Essential documents- Preparation, collation and QC
  • Ethics and regulatory submissions and approvals of the clinical trial application
  • Study Start up activities- site identification and selection, QC for IP release
  • Site Activation- SIV, ISF review and Drug supply review
  • Monitoring and Site Management
  • Study site close out activities

OBJECTIVES OF THE COURSE

To be able to:

  • Identify suitable Investigator for participate in a clinical trial.
  • Perform pre-selection visits to assess the suitability of a site to conduct the trial.
  • Understanding of what essential study documentation necessary are required start a trial
  • Conduct Pre-trial procedures including drug release IP
  • set up Investigational sites for conduct of the study
  • Conduct an initiation visit
  • Monitor the conduct at the investigational site
  • Review source documentation and site file review
  • Perform site management activities
  • Conduct a close-out visit at the end of the study. complete a clinical trial

Who is the course Designed For?

If you are a clinical trial administrator who has just been promoted to a CRA level or have limited experience as a CRA, this modular training is specifically designed for you. You may be a research nurse or a former data manager who has landed their first role as a CRA. This is a good starter course that will equip you with the skills to conduct clinical trial initiation and or/ monitoring and basic site management at the investigational site.

Share with friends

Date and time

Location

Citadines Holborn

94-99 High Holborn

London

WC1V 6LF

United Kingdom

View Map

Refund policy

No Refunds

{ _('Organizer Image')}

Organiser CGX Training

Organiser of Clinical Research Associates (CRA) Beginners Course

CGX TRAINING 

Dedicated to raising professionalism and standards in clinical trial management

Accredited Training Solutions for Clinical Trial Professionals

Companies that invest in training and development recognise the value of a skilled and motivated workforce. Training plays an essential role in building brand values and driving employee performance. And trained staff tend to repay their employer’s investment with greater professionalism, higher quality work and reduced staff turnover. 

In the pharmaceutical and healthcare sectors, training is increasingly demanded for compliance.  Regulatory inspections will report a lack of formal training, or inadequate training, which can result in negative outcomes for the organisations concerned, and their reputations.

CGX’s tailored training solutions provide end-to-end learning and development programmes for organisations of all sizes and individuals embarking on a career in the Clinical Trial sector. We are involved in every aspect, from identifying skills gaps to delivering practical training courses and provision of internationally recognised qualifications.  Our bespoke programmes are designed to improve marketing capability and build business advantage.

At CGX we use proven and best practice frameworks for training, which help empower trainees with confidence, skills, techniques and knowledge and assist companies to identify, design, deliver and evaluate training and implement a successful training strategy. 

Save This Event

Event Saved