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Analyst (Temporary) - United States  

Company managed [?] Still accepting applications
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Posted on : 15 April 2017

Project Description

BioMarin is the world leader in delivering therapeutics that provide meaningful advances to patients who live with serious and life-threatening rare genetic diseases. We target diseases that lack effective therapies and affect relatively small numbers of patients, many of whom are children. These conditions are often inherited, difficult to diagnose, progressively debilitating and have few, if any, treatment options. BioMarin will continue to focus on advancing therapies that are the first or best of their kind.

BioMarin Development Sciences collects biospecimens (human) during the execution of clinical trials through the various phases of drug development.  The ability to track and manage biospecimens from collection to final disposition with essential information such as informed consent and biospecimen collection compliance is crucial for BioMarin.  The Clinical Biospecimen Management group provides this support to the broader organization by ensuring that biospecimen-related activities are efficient, effective, and well-documents. 

The Analyst will focus on supporting the group in a planner role with responsibility for a limited number of studies and acting under the guidance of more experienced CBM staff.  Responsibility areas include serving as a point of contact for study team requests and escalating where appropriate, providing biospecimen-related input to stakeholder groups within BioMarin and maintaining the Biospecimen Management Plan (BMP).

Key Responsibilities:

-Primary point of contact on biospecimen management activities across all assigned studies

-Participate in Study Team meetings as a standing member

-Provide biospecimen-related input into vendor ctracts, SOWs, lab specificications, laboratory manuals, manifest

-Act as primary point of contact in resolving all biospecimen related queries

-Review biospecimen handling sections of ICF template

-Manage biospecimen tracking and reconciliation activities within the CBM systems

  • Experience within a laboratory and clinical trial setting's will benefit the candidate

    2 years of relelvant experience working in the pharmaceutical industry (including CROs, labs and biorepositories)

    Proficient with Excel/Word and Outlook is a must

  • BA/BS in health of life sciences or related degree


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We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.