Epidemiologist II
Title: Epidemiologist/ Associate Principal Scientist
Location: West Point, PA Duration: 18 months+ Description:
• Coordinate global COA/PRO strategic plans in support of Early Development Teams (EDTs), Clinical Trial Teams (CTT) and/or Clinical Sub-teams (CST) to assure alignment with product franchise goals. • Provide assistance on the selection and/or development of COA/PRO instruments for inclusion in studies. • Provide guidance on implementing COA/PRO instruments into studies by following *** standard processes. • Facilitate alignment of the selection of an appropriate endpoint measure to satisfy both regulatory and reimbursement needs. • Coordinate COA/PRO related sections of evidence packages to be submitted to regulatory and reimbursement agencies. • Coordinate the development, validation, implementation, and utilization of instruments aimed at measuring COA/PROs in the context of clinical trials and/or observational studies. • Conduct literature searches to support COA/PRO endpoint strategies. • Support/Produce scientific communications (abstracts, poster presentations, podium presentations, manuscripts, etc.) • Keep up to date with COA/PRO methodologies and guidelines (including those from regulatory authorities and reimbursement agencies) and communicate findings to cross-functional study teams as needed. Quals-- Actual Title: Associate Principal Scientist Department- Patient-Centered Endpoints & Strategy (PaCES) Qualifications: Education: • PhD in Health Services Research, Statistics, Psychometrics, Outcomes Research, or closely related field with 3+ years of relevant industry work experience in the Clinical Outcome Assessment (COA) field OR Master's Degree in Health Services Research, Statistics, Psychometrics, Outcomes Research, or closely related field with 5+ years of relevant industry work experience in the COA field OR Bachelor's degree in Health Services Research, Statistics, Psychometrics, Outcomes Research, or closely related field with 10+years of relevant industry work experience in the Clinical Outcome Assessment (COA). Required Experience: • Familiar with Clinical Outcome Assessment (COA) endpoint strategies, including Patient-Reported Outcomes requirements for regulatory and reimbursement agencies. • Knowledgeable of methodological approaches and technical aspects (i.e. study design, data analysis and interpretation) of COA/PRO development, validation, electronic migration and interpretation into clinical trial and observational studies. • Ability to understand and respond to multiple internal and external customers. • Strong project management and communication skills. • Experience with COA/PRO-related scientific presentations and publications. Software: MS office suite Personality: • Excellent communications skills. • Take initiatives to understand the role. • Curious about what we do. • Eager to understand more about this role. • Adapts well within the group. Note: • Work Location : West Point, Rahway (possibly) • Hybrid (3 days onsite between Monday-THRU) • Would be great to have more candidates with industry experience in this specific area. • Please provide gap explanation and complete work history with dates on the resumes submitted in the system. • Please add complete publications on the resume. If someone doesn't have publication, please mention it on the resume. Do not add references name and contact details on resume. | ||||||||