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Principal Content Steward job in Upper Gwynedd

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Merck & Co. jobs
Pennsylvania (PA), Upper Gwynedd
Job Code:  CLI007394-en_US
Employer:  Merck & Co.

Country:  United States
State:  Pennsylvania (PA)
City:  Upper Gwynedd

Requisition ID: CLI007394

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.

Position Description:

Seeking an individual with strong understanding of clinical study document content and the interrelationships of that content to develop structured content mapping for reuse. The individual will be responsible for decomposing clinical content and linking content for action (ie, by assigning relevant metadata and reuse policies). Merck has embarked on an effort within clinical to connect their clinical content for standardization to ensure the quality/consistency of their clinical documentation. The individual must fully understand the clinical development process, content library and governance concepts, as well as technology concepts and analytics.

The position is in the Clinical Development Medical Writing Department within the Clinical Content and Standards function. The activities will focus on content information and design, structured authoring, and acting as a steward for the structured authoring tool..

The Principal Content Steward is responsible for developing, implementing and managing structured content, authoring processes, developing clinical content standards (e.g., working with structured content, SDTM, TransCelerate, CDISC, ICH, governance, therapeutic libraries, tool requirements) to support all clinical regulatory writing portfolios. This person is expected to work mostly independently to achieve goals with minimal need for frequent direction.

Medical Writing writes various documents (eg Investigator Brochures, Clinical Study Protocols, and Clinical Study Reports) to start clinical studies, get our products approved, and maintain our products on the market. As a result, the individual will have an opportunity to learn about clinical development of pharmaceutical products and the regulations that govern how a product moves from research in humans to the market. The person should present as highly motivated with interests in medicine, pharmacology/pharmacy, or chemistry sciences, biological sciences or data/information management, as well as interests in writing and communicating medicine and science.

In this role the Principal Content Steward will:

• Have an advanced understanding of content standards
• Demonstrate advanced knowledge of end-to-end data and information flow
• Influence teams concerning SCA expectations
• Build talent within the workgroup, projects, and teams
• Participate in development of clinical study document content design and TA library standards
• Provide SME management of the definition, implementation, and maintenance of GCDS Standard Operating Procedures and supporting documentation to ensure compliance
• Answer clinical trial team questions regarding standards use and governance
• Define and maintain content design, therapeutic libraries, and template content adopted at Merck, in collaboration with standards development teams (e.g., Data Collection, CT, SDTM, ADaM, External Data)
• Define and oversee implementation of a standards communication plan
• Define, implement, track, and report on standards implementation metrics
• Lead moderately-sized content development projects independently and periodic reviews of resourcing procedures.
Required Core Competencies:

• Document Writing - advanced knowledge of content
• Document Management Systems - working knowledge
Soft Skills:

• Meeting - lead or actively participate
• Communication - advanced email skills with peers, direct reports, and managers
• Teams - lead or actively participate
• People Manage - manage individuals and their employee development
• Task Manage - own work, team activities, and other's development (manager)
• Quality - produce high-quality, timely documentation
• Problem Solving - Solve complex problems associated with MW scope of work, involving ambiguous situations across departments and the need to develop new options to resolve
• Team leader
• Project management skills
• Knowledge of management needs for different groups
• Training and awareness of behavioral needs
• Influencing and coordinating across organizations

• Understanding of the development and support process

Position can be based at a Merck location: Upper Gwynedd, Rahway, Boston or can be remote based.

Position Qualifications:

Education Minimum Requirement:

• BS degree with at least 7 years of pharmaceutical industry experience in one of the following areas: Clinical Development, Clinical Operations, Regulatory Submissions or Labeling (OR)

• MS degree or higher with at least 5 years pharmaceutical industry experience, in one of the following areas: Clinical Development, Clinical Operations, Regulatory Submissions or Labeling

Required Experience and Skills:

• Proficiency in Office applications and Project Management. Project application of Agile methodology preferred. Programming knowledge preferred. High degree of organization and ability to manage multiple projects at the same time
• Attention to detail and commitment to excellence in all aspects of work
• Excellent communication and interpersonal skills and ability
• Experience in structured content design and implementation
• Experience with Structured Authoring tools
• Knowledge of publishing process
• Participation in governance
• Ability to work in a team environment is required.
Preferred Experience and Skills:

• Knowledge of Sharepoint
• Ability to direct development teams
• Developed Tool specification and tested tools
• Experience in structured content design and implementation
• Experience with Structured Authoring tools
• The pharmaceutical development process and Touchpoints
• Producing guidance and communication
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 .

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:

EEOC Poster

EEOC GINA Supplement

Job: Clinical Research - Clin Ops
Other Locations: Boston, MA, US; Rahway, NJ, US
Employee Status: Regular
Number of Openings: 1
Shift (if applicable):
Hazardous Materials: No
Company Trade Name: Merck
ref: (CLI007394-en_US)
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