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In-House Clinical Research Associate

at Company: BioBridges LLC in Job Category: Clinical
posted on 8/21/08 12:00am

BioBridges provides consulting and contracting expertise to help emerging pharmaceutical, biotechnology and medical device companies successfully span The Clinical Divide(TM). We also offer flexible solutions to help CROs satisfy their ever-changing business demands.

By filling the voids in a company's existing capabilities, BioBridges spans The Clinical Divide(TM). From protocol development through phase IV, BioBridges ensures trials start off on the right path-and remain on it. As a result, we dramatically improve the likelihood of product success, agency approval and healthcare utilization.

Located in suburban Wellesley, in the heart of Massachusetts' biopharmaceutical community, BioBridges partners with emerging clinical organizations to "build bridges" between all areas of the clinical development lifecycle-from protocol inception, through execution and submission



Company Overview:
Our client is a medical device company based in Metrowest Boston.

Clinical Divide:
Our client has multiple clinical projects occurring and without the proper support will fall behind and miss key clinical goals in the next 12-18 months.

Responsibilities:
This role is for an in-house CRA who has had experience as a nurse or related background. They are looking for people who have worked in a hospital setting or operating room taking vitals, etc. There will typically be 20%-30% travel and can be as much as 50% travel depending on what project is going on. Travel would typically be to major US metropolitan areas but could occasionally be international.

They do not use CROs so are looking for their in-house CRAs to do basic study management including monitoring, site communications, CRF management, patient recruitment, understand lab data, reg. docs, etc.

Responsible for participating in all aspects of clinical trials including initiating, investigating and monitoring data collection. Evaluate, monitor, and document all study results. Ensures proper set up and maintenance of databases; to assure accurate statistical analysis and interpretation of study data. May be involved in establishing and maintaining device field trials (software and/or hardware related).

3-8 yrs clinical trial experience with a medical related background such as RN or related experience. Medical device experience is good to have but not required.

Scope:
In-house role. 40 hrs a week, with flexibility to work a day a week from home when they aren't traveling.

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