Pharma - Clinical Research Associate

Role overview

This opening is for a full-time remote Clinical Research Associate role supporting sponsor-dedicated studies. The selected professional will help run and coordinate clinical trials while making sure all activities align with applicable regulatory standards. A major part of the job is maintaining precise, complete study documentation and working in sync with the wider clinical research team to support trial delivery.

Qualifications

• A bachelor's degree in a relevant discipline, such as Life Sciences, Nursing, or another science-focused field.
• At least 1.5 years of experience in clinical research, preferably gained in a pharma or biotech environment.
• Working knowledge of ICH/GCP and FDA regulations, along with exposure to protocol development and study start-up.
• Strong organizational abilities and clear communication skills.
• Ability to perform effectively both independently and as part of a team.
• Good working knowledge of Microsoft Office tools, including Word, Excel, and PowerPoint.
• Prior use of clinical trial systems such as EDC and IWRS would be an advantage.
• Background in oncology or other therapeutic areas would be a plus.
• Strong problem-solving capability and sound decision-making skills.

Application note

Candidates were asked to send their CV to [email protected].