Medical Documentation Specialist
Há 5 dias
This is an exciting chance to contribute to a dynamic team as a Regulatory Submissions Coordinator. As part of the group, you will be responsible for providing day-to-day support activities, including collection of essential documents for ethics submissions and preparation of study documents to relevant authorities.
Key Responsibilities:- Collaborate with Regulatory Submission Managers and Start Up teams to ensure timely completion of tasks;
- Perform quality control checks on documents to maintain accuracy and compliance;
- Provide guidance and advice to internal and external team members on applicable regulations and requirements;
- Carry out additional tasks as needed to support the team's objectives.
- Bachelor's degree in a Life Sciences field (preferably) and at least 1-3 years of experience in regulatory submissions;
- Strong organizational and prioritization skills;
- Proficiency in Microsoft Office and attention to detail;
- Fluent communication skills in English, both spoken and written.
The organization is a leading clinical contract research organization dedicated to accelerating the global development of safe and effective medical therapeutics. With a presence in over 40 countries, we offer Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries.
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