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 and ultimately impact the lives of patients. 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 searching for a for a highly collaborative, knowledgeable and detail-oriented Program Manager.

This position may be located in either our Texas or NJ office. A remote working relationship may be considered for the right candidate.

Job Summary:

The Program Manager is a critical member of the Development team and will interact extensively with both internal stakeholders and external business partners. The selected incumbent will be responsible for vendor oversight for outsourced studies, managing vendor identification, budgeting, startup, and study close-out. In addition, they will review and tabulate data for slide preparations and reports, support regulatory filings, and coordinate meetings with internal and external partners, and track overall timelines to ensure successful execution.

Responsibilities:

• Managing external studies for ADME/PK, toxicology, pharmacology, and translational sciences
• Assisting clinical development in the conduct and reporting of clinical trials
• Compiling data from various resources to understand the disease landscape
• Assist in IND, NDA and other regulatory filings, as needed

Qualifications:

• Bachelor's degree in life sciences
• 3-5 years of experience in pharmaceutical R&D
• Prior experience in program management in clinical development
• Prior experience managing CRO vendors
• Excellent communication and interpersonal skills
• Strong excel skills
• Demonstrated ability to be resourceful and take initiative to drive projects forward
• Strong detail orientation and analytical skills
• Demonstrated experience working collaboratively in a team environment

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

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.