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Merck 2021 Medical Writing Content Steward Intern in North Wales, Pennsylvania

Job Description

The Future Talent Program features internships that lasts up to 12 weeks and will include one or more projects. These opportunities in our Research Division can provide you with great development and a chance to see if we are the right company for your long-term goals.

Our company's Global Clinical Trial Operations Clinical Content Standards team within the Medical Writing department is seeking individuals interested in exploring regulatory medical writing and who are fascinated with document content and the opportunity for content reuse, decomposing content, linking content for action, and making content smart.

This individual will:

  • Focus on operations ofstructured content management (SCM) tools supporting structured content authoringandcontentmanagement

  • Participateinand learn about the creation and governance of content models, templates, variables, libraries, metadata, and reuse policies that support structured content authoring processes and standardsfor ourclinical regulatory writing portfolios

  • Contribute to the development of presentations, abstracts and posters related to SCM

  • Learn about clinical development of pharmaceutical products and the regulations that govern how a product moves from research in humans to the market

Required Education and Experience:

  • Candidates must be currently enrolledandhave completedat least (1) year of a Masters of Science (MSc) or equivalent program OR at least (2) years of a PharmDwith a Bachelor of Science (BS), Engineering, or equivalent program.

  • Candidates must be available to work full-time for up to (12) consecutive weeks beginning in May or June of 2021.

Preferred Skills and Experience:

  • Candidates should have experienceinMicrosoft OfficeapplicationsincludingWord, PowerPoint, Excel, and One Note.

  • Candidates should have ability to work in acollaborativeteam environment.

  • Candidates should have complete fluency in reading and writing American English.

  • Candidates should have excellent communication and interpersonal skills.

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.

We are a research-driven biopharmaceutical company. Our mission is built on the simple premise that if we “follow the science” that great medicines can make a significant impact to our world. 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.

FTP2021

US and Puerto Rico Residents Only:

If you need an accommodation for the application process please email us at [email protected]

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

EEOC Poster at https://www.dol.gov/sites/dolgov/files/ofccp/regs/compliance/posters/pdf/eeopost.pdf

EEOC GINA Supplement​ at https://www.eeoc.gov/sites/default/files/migratedfiles/employers/eeocgina_supplement.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:

Intern/Co-op (Fixed Term)

Relocation:

No relocation

VISA Sponsorship:

No

Travel Requirements:

10%

Flexible Work Arrangements:

Flex Time, Remote Work

Shift:

1st - Day

Valid Driving License:

No

Hazardous Material(s):

Number of Openings:

2

Requisition ID: R75107

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