Clinical Project Associate

Job Description

As a Clinical Project Associate, you will be an integral part of our research team, overseeing clinical trials from inception to completion. You will liaise with stakeholders, manage timelines, ensure compliance with regulations, and support the execution of clinical protocols.

Responsibilities

• Implement systems for tracking project progress and compliance.
• Collaborate with cross-functional teams to enhance trial designs.
• Provide guidance to junior associates and interns.
• Help create and manage study budgets and forecasts.

Requirements

Education

• Bachelor's degree in Biomedical Science or a similar field

Experience

• 3+ years of experience in a clinical research environment

Technical Skills

• Project Management
• Documentation Management

Soft Skills

• Teamwork
• Time Management

Certifications

• Certified Clinical Research Coordinator (CCRC) is a plus

Languages

• English: Fluent

Advantageous

• Knowledge of statistical analysis techniques: Experience in applying statistics to clinical data.
• Previous involvement in global clinical trials: Experience in managing global multi-site studies.

Benefits

• Pension scheme with employer contributions
• Employee assistance program
• Generous annual leave policy
• Health and wellness initiatives

Company Culture

• Integrity and Trust: We uphold ethical standards in all our research and operations.
• Pioneering Spirit: We are dedicated to leading advancements in medical research.
• Community Engagement: We actively contribute to the wellbeing of the communities we serve.