Associate Clinical Research Specialist

Are you an organized and detail-oriented individual with a passion for the healthcare industry? Medtronic is looking for an experienced Associate Clinical Research Specialist to join our team and provide support in the coordination and management of clinical research studies.In this role, you will be responsible for monitoring the progress of clinical research studies and ensuring that all activities are conducted in compliance with regulatory requirements. You will collaborate with internal and external stakeholders to ensure that the studies are conducted on time and within budget.To be successful in this role, you must have a Bachelor’s degree in healthcare or a related field, as well as at least two years of experience in clinical research. Knowledge of Good Clinical Practices (GCP) guidelines and regulations is essential. You must be a self-starter with a high level of accuracy and attention to detail. You must also have excellent written and verbal communication skills and the ability to work independently and as part of a team.If you are looking for an opportunity to apply your experience and knowledge in the healthcare industry, we'd love to hear from you!

Responsibilities: • Monitor the progress of clinical research studies and ensure that all activities are conducted in compliance with regulatory requirements. • Collaborate with internal and external stakeholders to ensure that the studies are conducted on time and within budget. • Develop and maintain relationships with clinical research sites. • Prepare research documents and reports according to protocol guidelines. • Collect, analyze, and interpret data from clinical studies. • Monitor the implementation of clinical trial protocols. • Ensure that all study related documents are accurate and up-to-date. • Ensure that clinical data is entered into the appropriate database in a timely manner. • Assist in the review and preparation of protocols, consent forms, and other study documents. • Ensure that all regulatory documentation is completed properly. • Manage and coordinate all aspects of data management. • Ensure that all study data is maintained in accordance with GCP guidelines. • Provide training and guidance to research staff. • Assist in the preparation of study reports and other documents. • Assist in the development and implementation of safety procedures. • Maintain up-to-date knowledge of GCP and regulatory requirements.

According to JobzMall, the average salary range for a Associate Clinical Research Specialist in Duluth, GA, USA is $45,000 - $60,000 per year.

Medtronic plc is the world's largest medical device company that generates the majority of its sales and profits from the US healthcare system and is headquartered on the island of Ireland.