Overview
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 an 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 foster 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.
We are looking for a full-time employee, remotely based within the United Kingdom.
Job Specific Skills
* Mastery and train on generating tables, listings, and graphs from clinical trial databases using SAS.
* Utilizes System Development Life Cycle (SDLC) for programming deliverables.
* Advanced user in SAS programming, SAS Base, and SAS Macros.
* Advanced knowledge of E-Submission Standards, Guidelines and Regulations.
* Mastery and train on SDTM standards including ability to write specifications.
* Advanced knowledge of ADaM standards including supporting specification writing.
* Advanced experience with pooling of data sets for submissions.
* Advanced experience with BIMO outputs, define.xml, Reviewer's Guides, SDSP.
* Lead study or small programming project teams.
Job Requirements
* Educated to BSc or above within Computer Science, Mathematics or a Science related discipline.
* Minimum of 5 years’ experience in statistical programming, clinical programming, or similar field required.
* Ability to anticipate and effectively resolve potential problems with client demands.
* Line manages programming team members ensuring that everyone can reach their potential and identify their areas of development.
* Train and mentor less experienced team members
* Coach and encourage internal and external teams about best practices which bring additional value.
* Proficiency with MS Office applications.
* Hands-on experience with clinical trial and pharmaceutical development preferred.
* Good communication skills and willingness to work with others to clearly understand needs and solve problems.
* Excellent problem-solving skills.
* Good organizational and communication skills.
* Familiarity with current ISO 9001 and ISO 27001 standards preferred.
* Familiarity with 21 CFR Part 11, FDA, and GCP requirements.
* Basic understanding of CRO’s and scientific & clinical data/terminology, & the drug development process.
If you have not received a response within 14 days of your application, please consider your application unsuccessful.
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