Clinical Trial Coordinator, Experienced
Thermo Fisher ScientificFull Time
Senior (5 to 8 years)
Raleigh, North Carolina, United States
Key technologies and capabilities for this role
Common questions about this position
Yes, this is a remote position as a 'Work Anywhere' company supporting flexible work environments, with potential for future travel requirements.
This information is not specified in the job description.
Required skills include life sciences software programming experience, experience helping customers optimize EDC in clinical trials, and experience with Veeva CDB configuration and SQL programming.
Veeva Systems' values are Do the Right Thing, Customer Success, Employee Success, and Speed.
Strong candidates will have life sciences software programming experience, expertise in optimizing EDC for clinical trials, and hands-on experience with Veeva CDB configuration and SQL programming.
Quality and regulatory software solutions provider
Veeva Systems offers software solutions for quality, regulatory, and advertising claims management, focusing on consumer products and chemical companies. Their cloud-based platform provides visibility and traceability throughout the product journey, ensuring compliance with regulations and accelerating time-to-market. Unlike competitors, Veeva has specialized expertise in both the Life Sciences and Chemical sectors, allowing them to effectively address industry-specific challenges. The company's goal is to help clients efficiently bring safe and compliant products to market.