Precision Medicine Group is a global team of experts that specializes in precision medicine, which combines advanced lab sciences, translational informatics, regulatory affairs, payer insights, and marketing communications. The company focuses on overcoming product development and commercialization challenges for pharmaceutical and life sciences clients. Their services include biomarker-driven research and development, as well as commercialization support for life science organizations from launch to product maturity. Precision Medicine Group operates through two main arms: Precision for Medicine and Precision AQ, specializing in clinical and commercial solutions respectively.
1001 - 5000 employees
Founded 2012
𧬠Biotechnology
βοΈ Healthcare Insurance
π Pharmaceuticals
π° $35.2M Venture Round on 2021-03
February 8
πΊπΈ United States β Remote
π΅ $113k - $180k / year
β° Full Time
π Senior
π Data Scientist
π¦ H1B Visa Sponsor
Precision Medicine Group is a global team of experts that specializes in precision medicine, which combines advanced lab sciences, translational informatics, regulatory affairs, payer insights, and marketing communications. The company focuses on overcoming product development and commercialization challenges for pharmaceutical and life sciences clients. Their services include biomarker-driven research and development, as well as commercialization support for life science organizations from launch to product maturity. Precision Medicine Group operates through two main arms: Precision for Medicine and Precision AQ, specializing in clinical and commercial solutions respectively.
1001 - 5000 employees
Founded 2012
𧬠Biotechnology
βοΈ Healthcare Insurance
π Pharmaceuticals
π° $35.2M Venture Round on 2021-03
β’ The Senior Clinical Data Manager/Principal Clinical Data Manager manages all aspects of the clinical trial data management process from study start-up to post database lock for assigned projects. β’ Primary Data Management contact for assigned clinical project(s), ensuring tasks are performed in a timely manner. β’ Oversee project data entry process including development of data entry guidelines, training, and data entry quality. β’ Conduct database build UAT and maintain quality controlled database build documentation. β’ Train clinical research personnel on study specific CRF, EDC, and other project related items as needed. β’ Liaise with third-party vendors in a project-manager capacity in support of timelines and data-related deliverables.
β’ Bachelors and/or a combination of related experience β’ 8+ yearsβ experience for a Sr. Clinical Data Manager and 10+ years for a Principal Clinical Data Manager β’ Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook β’ Able to handle a variety of clinical research tasks β’ Excellent organizational and communication skills β’ Professional use of the English language; both written and oral β’ Experience in utilizing various clinical database management systems β’ Broad knowledge of drug, device and/or biologic development and effective data management practices β’ Strong representational skills, ability to communicate effectively orally and in writing β’ Strong leadership and interpersonal skills β’ Ability to undertake occasional travel
β’ Discretionary annual bonus β’ Health insurance β’ Retirement savings benefits β’ Life insurance β’ Disability benefits β’ Parental leave β’ Paid time off for sick leave β’ Paid time off for vacation
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