Imaging Lead (Sr. Principal Scientist)
Merck Sharp Dohme
Baton Rouge, LA (In Person)
Full-Time
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Job Description
- Job Description
- The Imaging Lead (Sr.
- Provide medical and scientific leadership in the use of clinical imaging in clinical development in broad categories of disease indications, or entire therapeutic areas.
- Interface with internal stakeholders and external collaborators (such as imaging service vendors) to ensure seamless execution and support for the imaging component of clinical trials.
- Design and oversee existing imaging strategies for early and late-stage clinical trial support.
- Exercise foresight and judgment in planning, organizing, and guiding complex imaging projects.
- Work across departments to advance imaging processes, and as needed, challenge the status quo to foster innovation.
- Work with quality and compliance teams for quality-related decision making internally, and assist with vendor audits as needed.
- In regulatory inspections, provide responses to any imaging-related information requests.
- Identify needs and lead internal initiatives and collaborations, with a focus on scientific innovation to advance the application of imaging in clinical development and decision-making.
- Make complex decisions and troubleshoot in ambiguous situations across departments.
- Regularly interact as an imaging subject matter expert with clinical management in early and late-stage clinical trials establishing a track record of successfully applying high level scientific judgement in complex situations
- Develop expertise and leadership in topics and processes that apply to and affect the entire program.
- Support industry presence for our company in clinical imaging at national meetings.
- May provide strategic direction through leadership of up to three direct reports.
- Qualifications, Skills & Experience
Education Minimum Requirement:
MD required.- At least 6 years of experience supporting clinical development in industry is preferred.
- Knowledge of the use of imaging in clinical trials for evaluation of efficacy and safety.
- Skill in authoring and reviewing imaging documents for clinical trials.
- Regulatory experience supporting drug filings.
Required Skills:
- Clinical Development, Clinical Medicine, Clinical Trial Development, Clinical Trials, Data Analysis, Imaging Technologies, Medical Imaging, Regulatory Compliance, Scientific Leadership, Scientific Publications, Strategic Leadership
Preferred Skills:
- Current Employees apply HERE (https://wd5.myworkday.com/msd/d/task/1422$6687.htmld) Current Contingent Workers apply HERE (https://wd5.myworkday.com/msd/d/task/1422$4020.htmld)
US and Puerto Rico Residents Only:
- Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities.
EEOC GINA
Supplement We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts (https://www.msdprivacy.com/us/en/CCPA-notice/) The salary range for this role is $282,200.00 - $444,200.00 This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee's position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for annual bonus and long-term incentive, if applicable. We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits . You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.San Francisco Residents Only:
- We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance
Los Angeles Residents Only:
- We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance
- Search Firm Representatives Please Read Carefully
- Merck & Co.
Employee Status:
- Regular
Relocation:
VISA Sponsorship:
Travel Requirements:
Flexible Work Arrangements:
- Remote
Shift:
Valid Driving License:
- Hazardous Material(s):
Job Posting End Date:
- 05/30/2026
- 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.
Requisition ID:
- R398379
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