Job Opportunity:
Clinical Research Associate
Description:
* Lead the execution of clinical research projects from design to closure, ensuring adherence to regulatory requirements.
* Coordinate with cross-functional teams to develop and implement project plans.
Key Responsibilities:
* Develop and maintain study-specific documents and tools, ensuring compliance with regulatory standards.
* Oversee the management of Trial Master Files and Investigator Site Files, guaranteeing accuracy and completeness.
* Collaborate with site qualification, study initiation, and study closure process teams to ensure seamless project execution.
* Track and report progress to stakeholders, utilizing data analysis to inform decision-making.
* Prepare high-quality study reports for regulatory submissions, demonstrating expertise in clinical research.
Requirements:
* Hold a Bachelor's degree in Science or a related field, with a strong foundation in clinical research principles.
* Possess 4 years of experience in the medical device industry, with a focus on pre-market and post-market clinical studies.
* Demonstrate expertise in problem-solving, communication, and project management skills, with a passion for driving clinical research forward.
This role is ideal for those seeking a challenging and dynamic environment where they can leverage their skills and expertise to drive clinical research success.