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Lexicon is a biopharmaceutical company with a mission of pioneering medicines that transform patients' lives. Through our unique approach to gene science based on Nobel Prize-winning technology, we are moving forward rapidly to bring innovative therapies to market. At Lexicon, our passion and dedication is driven by the patients for whom we work.

Lexicon employees are inspired by the idea that their work can improve patients' lives and we know that our employees are essential to the success of our mission. Every day they bring their passion, talents and dedication to an engaging environment where they are rewarded with opportunities to realize their potential. We are dedicated to making Lexicon a great place to work by providing employees with the benefits, services, and programs as part of our total rewards package. Join our journey and be a part of our multitalented team and make a difference in patients' lives!

Lexicon Pharmaceuticals is currently recruiting for a Clinical Systems Analyst. This role will be based in our Bridgewater NJ location.

The Clinical Systems Analyst will assist the Senior Director of Clinical and Development Systems in planning, directing, and coordinating software projects and support activities within the Drug Safety, Pharmacovigilance, Regulatory, Clinical Operations, and Quality Assurance groups. Responsibilities include managing, migrating, and supporting systems, data, and software projects such as the Veeva Safety, Veeva RIM, Veeva Submissions, Veeva PromoMats, and as well as overseeing related projects and support around those areas.

Responsibilities include, but are not limited to:

• Collaborating with Lexicon's Drug Safety, Pharmacovigilance, Regulatory, Clinical Operations, Quality Assurance, IT personnel, and vendors by:
  1. Leading support of their assigned software
  2. Supporting projects related to their assigned software
  3. Leading or supporting the integration of supported systems with study or partner systems
  4. Extracting information from the supported systems, formatting and inspecting the information, and sending the information and reports to the relevant departments
  5. Leading or supporting the validation of software systems
• Creating and updating SOPs, policies, and work instructions to comply with current processes and industry regulations for inspections
• Performing other assigned duties and special projects as needed

Qualifications:

• BA or BS in Business Information Systems, Management Information Systems or Computer Information Systems
• Previous substantive experience managing, configuring and supporting Drug Safety, Regulatory and Quality Systems
• 3 to 5 years of software project and/or software support
• An understanding of SQL or programming in object-oriented software
• Ability and desire to work in a team-oriented environment

For additional information about Lexicon and its programs, please visit www.lexpharma.com.

Lexicon is an Equal Opportunity Employer. We do not discriminate based on race, color, religion, sex, sexual orientation, gender identity, national origin, disability or status as a protected veteran.

Lexicon Pharmaceuticals, Inc. is a drug-free workplace. Candidates are required to pass a drug test, background check and verification of credentials before beginning employment.