About

Careers

At Cara Therapeutics, we are working to fundamentally change the way the world manages pain and pruritus.

In order to reach this worthwhile and lofty vision, it takes a team of intelligent, dedicated, and hard-working people to make it happen. We are always on the lookout for new talent. Explore the variety of opportunities available at Cara Therapeutics today:


Regulatory Affairs Manager

Cara Therapeutics, Inc. is looking for a full time Regulatory Affairs Manager with regulatory affairs and electronic submissions experience within the biotech and/or pharmaceutical industry. The ideal candidate must have prior experience managing an external publishing vendor, preparing electronic regulatory submissions and submission timelines. There will be opportunities to learn and contribute to regulatory strategy of development projects.

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Drug Safety Associate

Cara Therapeutics, Inc. is searching for a full-time Drug Safety Associate with experience to manage receipt and follow up of SAE reports from clinical sites, as well as book-in the cases in the safety database. Oracle Argus Safety database experience; knowledge of medical terminologies and the clinical trial process are highly desirable for this position.

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Associate Director, Clinical Project Manager

Cara Therapeutics, Inc. is searching for a full-time Clinical Project Manager with clinical operations/development related experience within the biotech and/or pharmaceutical industry. The ideal candidate will demonstrate a high level of core and technical competencies within the management of clinical trials. Management of CRO relationships and internal company timelines is a key aspect of this position.

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Head of Clinical Operations

Cara Therapeutics is looking to expand its clinical team. We are searching for an individual with clinical operations/development related experience within the biotech and/or pharmaceutical industry. The ideal candidate will demonstrate a high level of core and technical competencies within the management of clinical trials in the therapeutic area of Pain. The ability to self-start and be part of a cross-functional team with mentoring across a matrix environment and direct management experience is preferred. Management of CRO relationships and internal company timelines is a key aspect of this position. Experience with the conduct and management of both Phase 2 and Phase 3 trials a plus.

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Senior Medical Writer

Create/author and edit nonclinical, clinical and regulatory documentation. Prepare clinical reports, summary documents and other scientific documents that may be submitted to Regulatory authorities (FDA, EMEA), peer-reviewed journals or scientific meetings.

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