Job Description
Are you looking to join a company where your contributions truly matter, and where you’ll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.
Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit www.mmsholdings.com or follow MMS on LinkedIn.
- Job Responsibilities
- Gain experience with MS Office applications
- Learn ICH, 21CRF Part 11,ISO 9001 and ISO 7001.
- Gain exposure to eCRFs, CRF Completion Guidelines, Edit check specs, and DMP
- Contribute to study tracking and metric reports for use by the study team
- Contribute to user acceptance testing (UAT) of EDC and integrated systems including execution of test plan and scripts.
- Member of project team.
Job Requirements
- Bachelor’s Degree in a scientific, medical, or clinical discipline or related field is required; Master’s or PhD preferred
- 1-2 years of previous experience in clinical data management
- Hands-on experience with clinical trials and pharmaceutical development preferred
- Experience in the pharmaceutical or CRO industry must
- Experience with query and discrepancy management required
- Has a strong attention to detail
