CAREERS
Intarcia carefully maintains an environment based on our core values of innovation and integrity. We are comprised of talented and entrepreneurial people who enjoy collaborating and achieving excellent results. Our leaders are deeply experienced and extremely approachable executives who actively support our business plan and our team.
Our Company is committed to the following guiding principles:
- We value and respect each employee in the Company and treat one another as peers.
- We emphasize working hard, working together, and having fun.
- We encourage diversity in opinion, open discussions on issues and commit to allow one another to express their views.
Available Positions
Process Technician
Applicant must perform pharmaceutical manufacturing activities following cGMPs. Responsibilities include process equipment cleaning, set-up, and operation, as well as component assembly and
aseptic operations. Must follow written procedures, document all work in writing, and maintain safe work environment. Perform additional activities to support cleanroom operations, such as stocking supplies, water sampling, and environmental monitoring. Work requires high level of interaction with team members, including technicians, supervisors, engineers, and QA personnel. Must be able to work with small parts and able to perform a wide range of repetitive motions. Must be able to work evening or night shifts and be able to sit or stand for two to three hours at a time. Must be able to lift up to 50 lbs and push/pull up to 70lbs.
Please send resume and cover letter to careers@intarcia.com
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Associate Director of Clinical Operations
This position will be responsible for overseeing the direction, planning, execution, and interpretation of clinical trials research, data collection activities and clinical operations. In addition, the Associate Director of Clinical Operations will participate in design and implementation of clinical protocols, data collection systems and final reports; support new and ongoing clinical research and clinical trials and ensure efficient and timely processing of confidentiality agreements and clinical agreements; manage clinical and regulatory files; interact with investigational sites, clinical consultants, Contract Research Organizations and other vendors; and manage personnel to ensure the efficient operation of the function. Excellent and current knowledge of GCP, ICH and FDA regulations is expected. The successful candidate will have 10+ years experience of pharmaceutical experience and have prior involvement with multi-center, multinational Phase 3 trials. Experience in diabetes/metabolism is desirable. A life science/clinical background with an advanced degree (Ph.D. or M.D.) preferred.
Please send resume and cover letter to careers@intarcia.com
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To apply, contact: careers@intarcia.com
Benefits
Learn more about Intarcias benefits.
Benefits
