Clinical Data Manager Merrimack Pharmaceuticals
THIS JOB HAS EXPIRED
<br>Job Code : 165
Division : Merrimack
Location : Cambridge MA US 02139<br>Job Type : Full Time
Career Level : Experienced (Non-Manager)
Education : Bachelor's Degree
Category : Biotechnology and Pharmaceutical
Job Description :<br><p>Merrimack Pharmaceuticals is a privately held, biopharmaceutical company aspiring to be the leading provider of personalized medicines. Our company is advancing a suite of engineered therapeutics integrated with molecular diagnostics designed to address significant medical needs in the treatment of cancer and inflammation. Merrimack's integrated medicines (Rx & Dx) are products of a paradigm changing R&D platform, <i>Network Biology</i>, which integrates the technologies of engineering, biology, and computing to enable mechanism-based, model driven discovery and development of both therapeutics and diagnostics. We offer a highly collaborative, interdisciplinary environment in which the treatment of cancer patients and improving the current paradigm of drug development is paramount and central to all efforts.
<p>We have a career opportunity for a Clinical Data Manager who will be responsible for overseeing data management tasks from study start-up through database lock for development programs at Merrimack. This individual will be the main point of contact with CROs and other external vendors for all issues related to data management.</p>
<p>Specific responsibilities include:</p>
<ul><li>Reviewing and finalizing all DM related documents including Data Management Plan, edit check specifications, completion guidelines, and CRF design.</li><li>Data cleaning activities including listing review, external data reconciliation and data review</li><li>Managing a secure global data repository</li><li>Handling of external data and facilitating data transfers to internal and external stakeholders</li><li>Communicating with external vendors to define required file format and content specifications for electronic files</li><li>Overseeing database quality control activities</li><li>Working with the other functional groups within the project team (e.g. Biostatistics, Statistical Programming, Clinical Investigations, Clinical Operations, Research and Development)</li><li>Participating in the development and maintenance of SOPs and process guides related to data management activities</li></ul><br>Job Requirements :
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<ul><li>BA or BS degree with a minimum of 5 years of directly-related clinical data management experience.</li><li>Two or more years experience with oncology studies</li><li>Skilled in the use of EDC systems (Rave preferred) and reporting tools</li><li>Detailed understanding of project planning and management methods</li><li>Excellent interpersonal, communication, and organizational skills with the ability to work independently and in a team environment</li><li>SAS programming knowledge is highly preferred</li></ul><br>
| Location: |
Cambridge, MA 02139
United States
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THIS JOB HAS EXPIRED