Clinical Project Manager/Sr. Clinical Project Manager Job in Woodlands 77380, Texas US
Lexicon is a biopharmaceutical company focused on discovering and developing breakthrough treatments for human disease located in The Woodlands, Texas. We currently have five drug candidates in development for autoimmune disease, carcinoid syndrome, diabetes, glaucoma and irritable bowel syndrome, all of which were discovered by our world class research team. We have used our proprietary gene knockout technology to identify more than 100 promising drug targets. We focus drug discovery efforts on these biologically-validated targets to create our extensive pipeline of clinical and preclinical programs. Lexicon employees are inspired by the idea that their work can improve patients' lives and we know that our employees are important to the success of our mission. We are dedicated to making Lexicon a great place to work by providing employees with the benefits, services, and programs which will allow them to reach their full potential.
We are currently recruiting for a Clinical Project Manager/Sr. Clinical Project Manager in The Woodlands, Texas or Princeton, New Jersey office.
Job Summary:
This position will be responsible for overseeing the daily activities of Phase 1-3 world-wide clinical trials of drug candidates by ensuring that high quality and valid data supports regulatory applications and approvals of new-marketed products and indications. Responsibilities will include, but will not be limited to: managing Clinical personnel to conduct investigator identification, selection, training and routine monitoring; maintaining and negotiating vendor contracts; managing budgets and payments; serving as the study lead on Clinical project teams; participating in the design and development of clinical study protocols and CRFs across a range of therapeutic areas to ensure monitoring efforts fully complement the drug development process within established timelines; managing and executing trials through a combination of internal and external (CRO) staff; and other duties as assigned or required.
Qualifications:
- Bachelor's or Master's degree in a scientific related discipline
- Minimum of eight (8) years of clinical development experience in a pharmaceutical or clinical research organization
- Previous Clinical Project Manager experience in conducting and managing Phase 1-3 clinical trials
- Proficiency with Microsoft Office Suite
- Excellent organization and communication skills
- Ability and desire to work in a team-oriented environment
Interested candidates must apply through Lexicon's career website:https://lexicon-hr.silkroad.com/epostings/index.cfm?fuseaction=app.welcomecategory_id=36331company_id=16252version=1startflag=1parent=Clinical%20Developmentlevelid1=36331
For additional information about Lexicon and its programs, please visit www.lexpharma.com .
Lexicon Pharmaceuticals, Inc. is an equal opportunity/affirmative action employer.