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Merck Associate Director of Medical Writing, Oncology Publications in Rahway, New Jersey

Job Description

Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe, effective, innovative medicine.

The Associate Director works with scientists in our Company Research & Development (R&D) Division and external investigators to write or facilitate the writing of journal articles, conference abstracts, and posters/oral presentations that report our Company's clinical trial results and, at times, early-stage development and other scientific work, for timely peer-reviewed publication. In conjunction with other areas, including Clinical Research, Biostatistics and Research Decision Sciences (BARDS), Center for Observational and Real-world Evidence (CORE), Regulatory Affairs, Clinical Pharmacology, Translational Medicine, Drug Safety, and Basic Research, identify key issues for publications, define hypotheses and sources of data, and review data analysis plans for assigned franchise(s).

Primary Responsibilities

  • Be intimately familiar with science/literature of assigned therapeutic area(s). Develop and maintain an awareness of key data and insights regarding the emerging product profile and disease area within assigned therapeutic area(s). Be knowledgeable and conversant with most complex issues/questions in these areas, and able to discuss these issues/questions with opinion leaders and others as a peer.

  • Work with the Global Scientific and Medical Publications (GSMP) Publication Manager and members of the Publication Teams for assigned therapeutic area/franchise to execute the Publications Strategy Plan when a product candidate enters Phase III, or sooner. The plan will be incorporated in the Product Development Team’s (PDT’s) objectives and updated as appropriate.

  • Interact with GSMP Publication Managers to ensure adherence of Publication Teams to the Publications Strategy Plan.

  • Present and defend data at scientific forums and participate in our Company organized meetings, domestic and international, as appropriate.

  • Advocate our Company publication guidelines and other good publication practices and oversee the Office of Scientific and Technical Information Clearance (OSTIC) manuscript release process.

  • Ensure that franchise publication/presentation tracking information is accurately and actively maintained in Datavision and other relevant repositories.

  • Attend training courses and appropriate scientific meetings to maintain competency in and awareness of relevant external research activities.

Education Minimum Requirements

  • Medical Doctor (MD) or a Doctorate (PhD) or its equivalent in the biological sciences, biostatistics or epidemiology and a minimum of 5 years experience in scientific writing resulting in peer-reviewed publications or a Bachelor or Master of Science (BS/MS) and approximately 12 years of scientific writing experience resulting in peer-reviewed publications.

Required Experience and Skills

  • Demonstrated leadership and competence in biomedical research and strong writing skills

  • Understanding clinical pharmacology, clinical research methodology and biostatistics is mandatory

  • Oncology publications experience required

Preferred Experience and Skills

  • Industry (pharmaceutical industry and/or contract agency)

  • Proficiencywith Microsoft Office programs is expected, and familiarity with database programs and methods of data display is very helpful.

  • Immuno-oncology experience preferred

We are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we “follow the science” and that great medicines can make a significant impact to our world. And we believe that a research-driven enterprise dedicated to world-class science can succeed by inventing medicine and vaccine innovations that make a difference for patients across the globe.

Who we are …

Merck & Co., Inc., Kenilworth, New Jersey, USA is known as “Merck” in the United States, Canada & Puerto Rico. We are known as “MSD” in Europe, Middle East, Africa, Latin America & Asia Pacific. We are a global biopharmaceutical leader with a diverse portfolio of prescription medicines, oncology, vaccines and animal health products.

We are driven by our purpose to develop and deliver innovative products that save and improve lives. With 69,000 employees operating in more than 140 countries, we offer state of the art laboratories, plants and offices that are designed to Inspire our employees as we learn, develop and grow in our careers. We are proud of our 125 years of service to humanity and continue to be one of the world’s biggest investors in Research & Development.

What we look for …

In a world of rapid innovation, we seek brave Inventors who want to make an Impact in all aspects of our business, enabling breakthroughs that will affect generations to come. We encourage you to bring your disruptive thinking, collaborative spirit and diverse perspective to our organization. Together we will continue Inventing For Life, Impacting Lives while Inspiring Your Career Growth .

INVENT.

IMPACT.

INSPIRE.

NOTICE FOR INTERNAL APPLICANTS

In accordance with Managers' Policy - Job Posting and Employee Placement, all employees subject to this policy are required to have a minimum of twelve (12) months of service in current position prior to applying for open positions.

If you have been offered a separation benefits package, but have not yet reached your separation date and are offered a position within the salary and geographical parameters as set forth in the Summary Plan Description (SPD) of your separation package, then you are no longer eligible for your separation benefits package. To discuss in more detail, please contact your HRBP or Talent Acquisition Advisor.

If you need an accommodation for the application process please email us at staffingaadar@merck.com

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

EEOC Poster at https://www1.eeoc.gov/employers/upload/eeocselfprint_poster.pdf

EEOC GINA Supplement​ at https://www1.eeoc.gov/employers/upload/eeocginasupplement.pdf

OFCCP EEO Supplement at https://www.dol.gov/ofccp/regs/compliance/posters/pdf/OFCCPEEOSupplementFinalJRFQA508c.pdf

OFCCP Pay Transparency Rule at https://www.dol.gov/ofccp/pdf/pay-transp%20EnglishformattedESQA508c.pdf

We are an equal opportunity employer, Minority/Female/Disability/Veteran – proudly embracing diversity in all of its manifestations.

Search Firm Representatives Please Read Carefully

Merck & Co., Inc., Kenilworth, NJ, USA, also known as Merck Sharp & Dohme Corp., Kenilworth, 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:

Regular

Relocation:

No relocation

VISA Sponsorship:

No

Travel Requirements:

10%

Flexible Work Arrangements:

Telecommuting

Shift:

1st - Day

Valid Driving License:

Hazardous Material(s):

Number of Openings:

1

Requisition ID: R25024

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