Senior Scientist Drug Safety, Clinical Trial Safety Reporting:
Merck

DRU000770-en_US
Merck
Rahway New Jersey
Pharmaceutical
Description
Requisition ID: DRU000770

Merck & Co., Inc. Kenilworth, N.J., U.S.A. known as Merck in the United States and Canada, is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. The difference between potential and achievement lies in the spark that fuels innovation and inventiveness; this is the space where Merck has codified its legacy for over a century. Merck’s success is backed by ethical integrity, forward momentum, and an inspiring mission to achieve new milestones in global healthcare.


Merck is on a quest for cures and is committed to being the world’s premier, most research-intensive biopharmaceutical company. Today, we’re doubling down on this goal. Merck Research Laboratories is a true scientific research facility of tomorrow, and will take Merck’s leading discovery capabilities and world-class small molecule and biologics R&D expertise to create breakthrough science that radically changes the way we approach serious diseases. 


The Clinical Safety Scientist (CSS) in Clinical Trial Safety Reporting 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. Under the direction of the manager, the CSS will be responsible for intake, initial review, query management and creation of case reports for all reportable safety events according to standard operating procedures. In addition, the CSS will collaborate with cross- functional colleagues within clinical development, clinical operations, case processing and medical safety review. The CSS may participate in cross-functional or internal initiatives and/or process improvement projects.

Qualifications

Education: 
  • Advanced degree (M.S.) or equivalent Ex US degree in Life Sciences with 4+years’ work experience to include a minimum of 2 years relevant pharmaceutical, drug development/health sciences, and/or drug safety experience  -OR-
  • A 4-year BA/BS or equivalent Ex US degree in Life Sciences with 8+ years’ work experience to include a minimum of 3 years relevant pharmaceutical, drug development/health sciences, and/or drug safety experience.

Required: 
  • Strong understanding of scientific and medical concepts
  • Basic understanding of drug development
  • Knowledge of GCP and ICH regulations
  • Experience working as part of a cross-functional team setting
  • Effective problem solving skills
  • Must have excellent project management, time management/organizational skills
  • Strong communication skills with advanced oral and written English skills
  • Advanced computer/database skills

Preferred:
  • Experience in patient care setting
  • Experience in drug safety
  • Experience in pharmaceutical drug development 


Your role at Merck is integral to helping the world meet new breakthroughs that affect generations to come, and we’re counting on your skills and inventiveness to help make meaningful contributions to global medical advancement. At Merck, we’re inventing for life. 

 

If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to staffingaadar@merck.com.

  

Search Firm Representatives Please Read Carefully: 

Merck & Co., Inc. is not accepting unsolicited assistance from search firms for this employment opportunity.  Please, no phone calls or emails.  All resumes submitted by search firms to any employee at Merck via email, the Internet or in any form and/or method without a valid written search agreement in place for this position will be deemed the sole property of Merck.  No fee will be paid in the event the candidate is hired by Merck as a result of the referral or through other means.

 

For more information about personal rights under Equal Employment Opportunity, visit:

 

            EEOC Poster

            EEOC GINA Supplement 



Job: Drug/Dvcs Sfty Survnce (NonMD)
Other Locations:
Employee Status: Regular
Travel: Yes, 5 % of the Time
Number of Openings:
Shift (if applicable):
Hazardous Materials:
Company Trade Name: Merck
Basic Qualifications
Requirement