2018 MRL Medical Writing Intern Job
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.
Research Lab is currently seeking a highly motivated individual with interests
in medicine, pharmacology/pharmacy, or biological sciences, as well as interest
in copy editing, data verification, and formatting of communications in
medicine and science. The goal of this internship is to gain broad insight into
the drug development process, knowledge of clinical regulatory documents, and
hands on experience in clinical technical editing. The Medical Writing
department is responsible for creating documents that report the results of
clinical trials in subjects receiving investigational Merck products to
regulatory agencies in the U.S. and worldwide. These documents include clinical
study protocols, clinical study reports, Investigator Brochures, and overall
summaries of clinical programs. The Medical Writing department works in all of
Merck’s therapeutic areas, including oncology, infectious disease, cardiology,
diabetes, and neurology. The intern will work on a project that will give
him/her individual and team experience with how clinical trials are designed,
analyzed, and reported. He/she will work
under the guidance of a mentor and have observational as well as hands-on
Candidates must be currently enrolled in a BS or BA degree program in the
life sciences or a field related to writing or editing.
must have completed (3) years of study prior to June 2018.
must be returning to school in the Fall of 2018.
must be available to work full-time for 9-12 weeks beginning in May or June
must have some technical expertise in Microsoft Office (advanced Microsoft
Word, including the use of electronic Word templates) or Adobe Acrobat.
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 an accommodation for the application process please email us at firstname.lastname@example.org.
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.
Visa sponsorship is not available for this position.
For more information about personal rights under Equal Employment Opportunity, visit:
Job: Clinical Research - Clin Ops
Employee Status: Temporary
Number of Openings:
Shift (if applicable):
Company Trade Name: Merck