Senior Clinical Research Associate

In brief

**Overview** This role is for a Senior Clinical Research Associate (SCRA) or Clinical Research Associate (CRA) at ICON. The position involves designing and analysing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. The role is based in and around Johannesburg. **What you will do** You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively. Key responsibilities include: * Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials. * Ensuring protocol compliance, data integrity, and patient safety throughout the trial process. * Collaborating with investigators and site staff to facilitate smooth study conduct. * Performing data review and resolution of queries to maintain high-quality clinical data. * Contributing to the preparation and review of study documentation, including protocols and clinical study reports. **Requirements (from the original advert)** * Bachelor's degree in a scientific or healthcare-related field. * Minimum of 3 years of independent monitoring experience as a Clinical Research Associate for CRA II level role. * Minimum of 5 years independent monitoring experience as a Clinical Research Associate for SCRA level role. * In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. * Strong organizational and communication skills, with attention to detail. * Ability to work independently and collaboratively in a fast-paced environment. * Willingness to travel as required approximately 60%. **Who should apply** Candidates with relevant clinical trial monitoring experience and a Bachelor's degree in a scientific or healthcare-related field are encouraged to apply. The ideal candidate will possess in-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. They should demonstrate strong organizational and communication skills, attention to detail, and the ability to work both independently and collaboratively in a fast-paced environment. A willingness to travel approximately 60% is also required. Specific experience includes a minimum of 3 years of independent monitoring for a CRA II level role or 5 years for an SCRA level role. **Deadline** Not specified **Reference** Original posting: https://www.myjobmag.co.za/job/senior-clinical-research-associate-icon-plc Source: myjobmag

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At a glance

• At least 3 years of experience.

• Google Cloud

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