We are recognised as a Deloitte Fast 50 company, Westpac Business award winner, and a Focus company for NZTE.

About the role: Optimal Clinical Trials seeks an experienced study coordinator who is motivated, organised and has a 'can do' attitude.

You will have the opportunity to be part of an exciting and growing research organisation where no two days are the same.

Duties and responsibilities:

The study coordinator is responsible for managing clinical research trials and conducts the running of the trials along with other team members.

This includes effectively setting up the research study, recruiting participants, coordinating and conducting participants visits, through to study close out. All work is carried out in accordance with the study protocol, ICH GCP guidelines and Standard Operating Procedures.

You will be joining a supportive team in a growing organisation.

We are seeking the following key skills, experience and attributes:

• MUST have experience in clinical research ideally as a study coordinator
• Enthusiastic, motivated and highly organised
• Efficient and with a proactive, 'can do' attitude
• Excellent communication skills
• Able to work autonomously and a good team player
• Experience with ICH GCP guideline requirements
• Professional in experience and nature, confidently communicating with our study sponsors and participants
• Clinical/nursing background preferred

Why work for us? 

We are in an exciting sector that has huge opportunities for growth. Our team is dedicated, talented, deliver world class research and care about each other and our wonderful patients. Our core values of putting people first, acting with integrity, working in partnership, creating value through continuous improvement, high performance and timeliness drive our beliefs, actions and results. We also make sure to have fun, and have a supportive and collaborative company culture