Clinical Trial Assistant (CTA)

We are looking for a highly motivated and detail-oriented individual with 0 to 7 years of experience to join our team as a Clinical Trial Assistant (CTA) in the Pharmaceutical & Life Sciences industry. The ideal candidate will have excellent communication skills and be able to work effectively in a fast-paced environment.

• Assist in planning, coordinating, and executing clinical trials to ensure compliance with regulatory requirements.
• Develop and maintain study protocols, case report forms, and investigational reports.
• Collaborate with cross-functional teams including investigators, statisticians, and medical writers to achieve study objectives.
• Conduct site feasibility assessments and coordinate with investigators to ensure timely and accurate data submission.
• Provide administrative support to the project team including data entry, document review, and report generation.
• Ensure adherence to Good Clinical Practice (GCP) guidelines and maintain accurate records of all study activities.

• Bachelor's degree in any discipline or equivalent qualification.
• Strong understanding of clinical trial conduct, GCP guidelines, and regulatory requirements.
• Excellent communication, organizational, and problem-solving skills.
• Ability to work independently and collaboratively as part of a team.
• Proficiency in Microsoft Office applications including Word, Excel, and PowerPoint.
• Familiarity with clinical trial management systems (CTMS) is an advantage.