Clinical Trial Supply Management Assistant

Work Schedule: Monday-Friday, 8-5 PM (no overtime expected)

Pay rate: $21+/hr

We are hiring a document controller to join the Clinical Trial Supply Management Team to work with-in supply management for one of our premium pharmaceutical clients in Indianapolis, Indiana.

The Clinical Trial Supply Management Assistant is responsible for processing New Site Readiness forms to establish new clinical trial sites. This is a critical function in the clinical trial process. The successful candidate will work closely with several teams, including the Supply Management team, to ensure readiness to treat patients. Additional data entry based tasks are also involved in the role. Excellent communication skills, attention to detail, and a commitment to accuracy in data processing are essential to success.

Keywords provides a competitive compensation package, good benefits and a casual, fun, productive and supportive working environment. We empower people to perform to the best of their ability with our “can do” attitude. We appreciate and embrace flexibility and learn at every opportunity to grow ourselves through experience, training and tackling new challenges.

Requirements

• Attention to detail
• Comfort in communicating via email
• Ability to prioritize and communicate priorities
• Demonstrated ability to learn computer systems and follow Standard Operating Procedures
• Previous experience in pharma or health care is beneficial but not required
• Basic Excel skills (data entry only)

Benefits

Keywords provides all its contingent workforce with:

• Medical, dental and vision benefits
• Paid time off (including sick leave and select holidays)
• 401(k) enrollment with 3% employer matching

Last updated on Aug 13, 2024