2025 University Recruiting - Chemoproteomics Co-op (Proteomics Data Analysis) - Military Veterans
at Merck & Company
Job Description
Under the general direction of the Patient-Centered Endpoints & Strategy (PaCES) group lead, the Principal Scientist has responsibility for supporting or co-leading global Clinical Outcomes Assessment (COA) endpoint strategies, including Patient-Reported Outcomes for specific disease areas. The individual will co-lead or guide teams on the development, validation, analysis and interpretation of COA endpoints to support regulatory submissions, reimbursement evidence dossiers, payer interactions, and publications. The Principal Scientist will work closely with individuals from Clinical Research, Regulatory Affairs, Biostatistics, Outcomes Research, and Operations to ensure COA endpoint strategies are consistent with and executed and interpreted to support the product strategy.
Primary activities include but are not limited to:
- Collaborate in global COA endpoint strategic plans with Early Development Teams, Value & Implementation and Clinical Sub-teams to assure alignment with product franchise goals
- Execute and standardize COA-related activities including
- Coordinate and lead the development, validation, analysis, interpretation and utilization of instruments aimed at measuring COAs in the context of clinical trials and/or observational studies
- Provide guidance, create and/or review dossiers to be submitted to Regulatory Authorities and/or Health Technology Assessment (HTA) agencies to assure consistency and alignment with COA strategies and represent our company during these interactions
- Provide guidance on sections of protocols, analysis plans and reports related to COAs
- Work closely with the cross-functional study team to interpret results from COA endpoints
- Collaborate on quantitative analyses of COA data to inform endpoint strategies and produce development
- Maintain awareness of scientific, regulatory, and market access developments within their areas of expertise across our company's functional areas, both in terms of new methodology and new activities to establish communication with key outcomes research opinion leaders
- Organize the collection of existing information on COAs used in both internal and external studies to facilitate selection and/or development of measures
- Provide training on COA-related company groups, as needed
- Support or produce scientific communications (abstracts, poster presentations, podium presentations, manuscripts, etc.) and external communications (e.g., value evidence dossiers)
- Keep up to date with methodologies and guidelines (including those from regulatory authorities and reimbursement agencies) and communicate findings to cross-functional study teams as needed
Qualifications
Education:
- PhD in Health Services Research, Statistics, Psychometrics, Outcomes Research or closely related field with 5+ years of relevant 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 7+ years of relevant work experience in the COA field OR Bachelor's Degree in Health Services Research, Statistics, Psychometrics, Outcomes Research or closely related field with 15+ years of relevant work experience in the COA field (including 10+ years in industry)
Required Experience and skills:
- Strong knowledge of methodological approaches and technical aspects (i.e. study design, data analysis and interpretation) related to COA development, validation, electronic migration and interpretation to support clinical trials and observational studies
- Experienced in COA/PRO requirements for regulatory and reimbursement agencies
- Able to drive COA-related quantitative analyses with cross-functional teams
- Able to develop strong internal relationships with cross-functional teams
- Able to understand, interact and responds to multiple internal and external customers
- A track record of COA-related scientific presentations and publications
NOTICEFORINTERNALAPPLICANTS
In accordance with Managers' Policy - Job Posting and Employee Placement, all employees subject to this policy are required to have a minimum of twelve (12) months of service in current position prior to applying for open positions.
If you have been offered a separation benefits package, but have not yet reached your separation date and are offered a position within the salary and geographical parameters as set forth in the Summary Plan Description (SPD) of your separation package, then you are no longer eligible for your separation benefits package. To discuss in more detail, please contact your HRBP or Talent Acquisition Advisor.
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Expected US salary range:
$181,600.00 - $285,800.00
Available benefits include bonus eligibility, long term incentive if applicable, health care and other insurance benefits (for employee and family), retirement benefits, paid holidays, vacation, and sick days. A summary of benefits is listed here .
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Employee Status:
Regular
Relocation:
Domestic
VISA Sponsorship:
Yes
Travel Requirements:
10%
Flexible Work Arrangements:
Not Applicable
Shift:
Not Indicated
Valid Driving License:
No
Hazardous Material(s):
n/a
Job Posting End Date:
10/21/2024
*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
New York, NY
Today's Merck is a global healthcare leader working to help the world be well. Merck is known as MSD outside the United States and Canada. Through our prescription medicines, vaccines, biologic therapies, and consumer care and animal health products, we work with customers and operate in more than 140 countries to deliver innovative health solutions. We also demonstrate our commitment to increasing access to healthcare through far-reaching policies, programs and partnerships. For more information, visit www.merck.com.