Scientist Drug Safety (Temporary)

Job Description

The Scientist Level Clinical Safety Scientist (CSS) is responsible for support of safety reporting in clinical trials conducted in multiple therapeutic areas as part of investigational product development programs across early and late-stage development.  Assists the protocol lead in safety reporting activities for multiple clinical trials. The CSS may support collaboration with cross-functional colleagues within clinical development, clinical operations, case processing and medical safety review.     

Key Responsibilities:

• Intake of reportable safety event information from clinical trial investigator sites.

• Review and manage individual case safety reports for each event.

• Ensure that all information required for a clinically complete and accurate case is present.

• Generate safety queries to the trial investigator sites to ensure case report accuracy and completeness.

• Prioritize daily work to ensure all events are submitted for entry into the safety database within the established timeframes.

• May collaborate with cross-functional colleagues as needed.

• Complete protocol-specific activities as required.

• Actively participate and ensure effective communication with the protocol lead and other team members supporting their protocols.

• Appropriately escalate protocol or individual event issues with other stakeholders, including CRAs/CRMs or protocol leads.

Qualifications & Skills

• Understanding of scientific and medical concepts

• Basic understanding of drug development

• Basic knowledge of GCP and ICH regulations

• Ability to work as part of a cross-functional team.

• Ability to identify and escalate problems and contribute to issue resolution.

• Time management and organizational skills.

• Strong communication skills with advanced oral and written English skills.

• Advanced computer and database skills

• Independent, strong analytical, and problem-solving skills

• Able to work under the pressure, strong sense of responsibility and accountability.

Education Requirement:

• M.D./D.O. or equivalent degree in Medicine

• 1 year of experience in a patient care setting, drug safety or 2 years of relevant pharmaceutical, drug development or drug safety experience

*Please submit your CV in English

Required Skills:

Accountability, Biological Sciences, Clinical Development, Clinical Reporting, Clinical Safety, Clinical Trials, Clinical Trials Monitoring, Cross-Functional Collaboration, Detail-Oriented, Drug Development, English as a Foreign Language, Life Science, Pharmaceutical Development, Pharmacotherapeutics, Pressure Management, Product Development, Teamwork, Time Management, Works Under Pressure

Preferred Skills:

Safety Reporting

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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:

Project Temps (Fixed Term)

Relocation:

VISA Sponsorship:

Travel Requirements:

Flexible Work Arrangements:

Hybrid

Shift:

Valid Driving License:

Hazardous Material(s):

Job Posting End Date:

07/17/2026

*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.