Clinical Research Associate at Clintec

Responsibilities Of The Clinical Research Associate (CRA)

• Perform all types of site visits (selection, initiation, interim and close out)
• Work in accordance with company SOPs, GCP guidelines and country specific regulations
• Site management activities to ensure adherence to protocol, SDV and CRF
• Develop, collect, review and edit clinical trial documentation
• Assist in protocol design as and when required
• Ensure adequacy of drug shipment and drug accountability
• Liaise and form positive working relationships with all colleagues, study site staff and sponsor representatives
• Work closely and provide support to the study Project Manager
• Organise and/or attend investigator meetings

Criteria

• Bachelor’s degree level (or equivalent) within Medicine, Biological Sciences, Pharmacology, Nursing or relevant life science discipline
• Significant experience within CRA role across a range of therapeutic areas
• Work experience within a pharmaceutical company or CRO setting
• Good working knowledge of ICH GCP and local regulatory requirements
• Ability to independently perform all types of site visit (selection through to close out)
• Fluency in English and Afrikaans languages required
• Willing and able to travel to sites across South Africa

Why Work For Clintec?

At Clintec, we believe our people are our greatest asset and understand that the best performance comes from individuals who know they are part of a valued team. You can expect to receive expert training and guidance throughout your career with us, with the opportunity to develop, progress and travel globally.

We Can Offer You

• A competitive salary and benefits package
• The opportunity to work with various global pharmaceutical leaders on the some of the most prestigious, ground-breaking and challenging drug development projects
• Real career development opportunities and a life-long career with an innovative, forward-thinking clinical research company