Summary written by USA Jobs 24 from Merck's advert and our data on 16,898 current US jobs. How we check every job
At a glance
Merck is hiring a Senior Principal Scientist, Drug Safety in Rahway, NJ; Upper Gwynedd, PA. It is a full-time fully remote role in Healthcare & Life Sciences, asking for at least 3 years of experience, first listed on November 11. The advertised pay is $282,200–$444,200 a year. The description mentions Statistics. Merck has 99 other openings in the US, 45 of them in Rahway, NJ. Across all employers on USA Jobs 24 there are 19 Healthcare & Pharma openings in Rahway, NJ today; the typical one asks for 5 years and advertises about $271,000 a year at the midpoint.
How the pay compares
Merck advertises $282,200 to $444,200 a year, a midpoint of $363,200 a year. Where an offer lands in a range usually depends on experience and on the exact location. That is higher than about 88% of the 33 healthcare & pharma jobs in New Jersey that publish a yearly rate on USA Jobs 24, where the typical midpoint is $246,000 a year. To see roughly what this leaves after federal and New Jersey tax, try our take-home pay calculator.
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Before you apply
- Check it is still open. We found this job on Merck's Workday site on November 11 and checked it again November 11, 5:17 AM ET. When an employer takes a job down, we remove it at our next daily update.
- Check where you can work from. This job is listed as remote. Many US employers can only hire remote staff in states where they run payroll, so look for a list of states in the advert below.
- Match the experience. The advert asks for at least 3 years of experience. If you are a little short, a close match on the skills in the advert can still win an interview.
- Tailor your resume. Use the advert's own words, such as Statistics, wherever they are true for you. Our resume guide shows how.
- Know your number. Decide the lowest offer you would accept before the first call. Our salary negotiation guide explains how to ask for more.
- Apply only through Merck's own site. Our Apply button goes straight to Merck's Workday page. If anyone contacts you about this job and asks for money, gift cards or bank details, stop and check it with our scam checker. Read how to spot a fake job offer.
About hiring at Merck
Merck has 100 openings on USA Jobs 24 today across 16 states. Most are in healthcare & pharma (23), data & AI (12) and software & IT (12). The biggest locations are Rahway, NJ (46), North Wales, PA (24) and Upper Gwynedd, PA (16). 10% of them are remote, 8% are open to entry-level candidates and 94% show pay. We collect Merck's jobs every day straight from its own careers system (Workday), never from job boards or agencies.
The employer's advert
This is Merck's own description of the job, copied word for word from its careers site. We have not edited it.
Show the full advert from MerckHide the advert1,194 words
Job Description
Position Overview:
The CSRM Physician is a leader in pharmacovigilance and is responsible for the overall clinical risk management and safety surveillance of assigned investigational and marketed products. As chairs of the Risk Management Safety Team, CSRM physicians lead the development and maintenance of risk management and pharmacovigilance plans.
Primary Activities:
· Engage directly in product development activities via core membership on Product Development Teams and chairmanship of the Risk Management and Safety Team, and other related sub-team participation, for assigned products. This may include participation in internal and joint internal/external research project teams relevant to the development of new compounds and the further study of marketed compounds.
· Partners with clinical development to ensure that clinical programs will support robust safety assessment of investigational compounds. Works with Clinical Research to develop the benefit-risk evaluation in aggregate safety reports.
· The CSRM Physician works closely with cross-functional team members including those from clinical development, epidemiology, regulatory affairs, statistics, and manufacturing to manage safety topics under evaluation to ensure efforts are aligned to meet global pharmacovigilance and risk management strategies for assigned products.
· Duties include all aspects of safety data evaluation, including assessing safety from multiple sources, e.g., clinical trials, literature and post-approval use and ensuring completeness of safety information in company core data sheets.
· Accountable for scientific strategy for safety related documents (e.g., CTD components, Risk Management Plans and Periodic Safety Update Reports) and for ensuring that the safety sections of Company product circulars are medically and scientifically appropriate.
· Responsible for safety surveillance activities for assigned products such as aggregate clinical trial data analysis and post approval safety signaling reviews, using medical judgment in review of aggregate data and individual cases. Collaborates with CSRM Associate in the oversight of safety surveillance activities for assigned products.
· Responsible for risk management activities such as contributing to recommendations for pharmacovigilance actions, making recommendations for labeling, and developing the Risk Management Plans, pharmacovigilance strategies and risk minimization activities in collaboration with CSRM Associate.
· Oversees the review and approval of product labeling files stored in the safety database and demonstrates a working knowledge of MedDRA.
· The CSRM Physician prepares safety summaries and analyses of safety related data for regulatory documents, aggregate reports, and summaries in support of regulatory filings and may supervise the activities of CSRM medical associates in the execution of safety data analysis and authoring of regulatory documents.
· Participates in the development, implementation and evaluation of standards, processes, metrics, and other department initiatives.
Education:
· Required: MD, DO, or equivalent
· Preferred: Board Certification
Required Experience and Skills:
· Minimum of 3 years clinical experience following post-graduate medical training or other relevant clinical experience
· Prior experience in drug development (may include clinical development and/or regulatory)
· Experience in clinical safety, pharmacovigilance and/or risk management
· Demonstrated organizational leadership skills, preferably in the employment areas noted above.
· Excellent communication, writing and analytic skills
Required Skills:
Clinical Development, Clinical Risk Management, Clinical Safety, Clinical Training, Drug Development, Drug Safety Surveillance, Pharmacovigilance, Regulatory Documents, Risk Management, Safety Assessment ReportsPreferred Skills:
Current Employees apply HERE
Current Contingent Workers apply HERE
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. Please click here if you need an accommodation during the application or hiring process.
As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:
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
The primary location for this posting is:
USA - New Jersey - RahwayWhere required by law, the compensation range for this role is provided below.
The salary range for the primary location of this role is:
$282,200.00 - $444,200.00This range reflects the Company's reasonable expectation of the base salary applicable to this role at the time of 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.
Additional location(s): Please note the salary range above applies to the Primary Location of the position. Where a role has other listed locations, different compensation guidelines may apply. You may find the salary ranges for additional locations below. If the salary range is not listed for the location you are applying to, our Talent Acquisition team will provide further information to you relevant to your location.
Additional location(s) Compensation Information:
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., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Employee Status:
RegularRelocation:
No relocationVISA Sponsorship:
NoTravel Requirements:
10%Flexible Work Arrangements:
RemoteShift:
Not IndicatedValid Driving License:
NoHazardous Material(s):
n/aJob Posting End Date:
11/14/2026*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.
USA Jobs 24 copied this listing from Merck's official careers site on November 11, 2026 and checked it again November 11, 5:17 AM ET. Merck will never ask you to pay to apply or to buy equipment with a check they send you. If anyone does, it is a scam.
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