About OPIS
OPIS is a full-service Contract Research Organization (CRO) supporting pharmaceutical, biotechnology and medical device companies worldwide. With expertise across Clinical Operations, Biometrics, Medical Writing, Pharmacovigilance and Regulatory Affairs, we partner with sponsors to deliver high-quality clinical research solutions across all phases of development.

OPIS is proactively building a talent pool of experienced Clinical Research Associates (CRAs) to support future business growth. While this is not an active vacancy, we are interested in connecting with professionals who would like to be considered for future opportunities within our Clinical Operations team.

Areas of Expertise We're Interested In

• Site selection, qualification, initiation, monitoring and close-out visits
• Clinical trial monitoring in accordance with ICH-GCP and regulatory requirements
• Site management and investigator relationships
• Source data verification (SDV) and quality oversight
• Risk-based monitoring approaches
• Protocol and regulatory compliance
• Clinical trial documentation and Trial Master File (TMF) management
• Site training and support
• Cross-functional collaboration with Project Management, Data Management and Regulatory teams

Ideal Background
We would love to hear from professionals who have:

• A Bachelor's degree in Life Sciences, Pharmacy or a related scientific discipline
• Experience working within a CRO environment
• Previous Clinical Research Associate (CRA) experience
• Strong understanding of ICH-GCP and clinical research regulations
• Willingness and ability to travel as required
• Full right to work in the country of employment
• Fluent English communication skills

Please note: This opportunity is intended for talent pooling purposes only and is not linked to an active vacancy. If a suitable opportunity arises that aligns with your background and experience, a member of our Talent Acquisition team may contact you to discuss potential next steps.

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