Guaduas, Cundinamarca, Colombia · On-site
$142k–$224k/yr
Job Description The Clinical and Regulatory Strategic Communications (CRSC) department within GCTO creates and delivers high-quality regulated content in support of our development pipeline and enables data sharing for o…
Skills: Clinical Data, Clinical Development, Clinical Study Design, Clinical Trial Compliance, Ich Gcp Guidelines
Rahway, New Jersey, United States · Hybrid
$142k–$224k/yr
Job Description As our company continues to modernize content, customer engagement, and AI-enabled ways of working, we are taking a "One our company" approach to simplify processes, accelerate value delivery, and enable …
Skills: GenAI, Agentic AI, Strategic Programs, Digital Transformation, Product Management
Rahway, New Jersey, United States · Hybrid
$142k–$224k/yr
Job Description As our company continues to modernize content, customer engagement, and AI-enabled ways of working, we are taking a "One our company" approach to simplify processes, accelerate value delivery, and enable …
Skills: GenAI, Agentic AI, Digital Transformation, Strategic Program Management, Agile Project Management
North Wales, Pennsylvania, United States · On-site
We’re seeking an Assistant Store Manager to join our team to help with store operations, customer service and team development. Duties include, but are not limited to, the following: Assist with store functions and day-t…
Skills: Store Management, Customer Service, Team Development, Inventory Management, Loss Prevention
Guaduas, Cundinamarca, Colombia · On-site
$142k–$224k/yr
Job Description The Clinical and Regulatory Strategic Communications (CRSC) department within GCTO creates and delivers high-quality regulated content in support of our development pipeline and enables data sharing for o…
Skills: Clinical Data, Clinical Development, Clinical Study Design, Clinical Trial Compliance, Ich Gcp Guidelines
North Wales, Pennsylvania, United States · Remote OK
$79k–$125k/yr
Job Description Job Description: As a Cardiovascular Disease Specialist, you will drive meaningful patient impact by leveraging our scientific expertise and serving as the primary contact for customers within your assign…
Skills: Account Management, Adaptability, Biotechnology, Business Planning, Cardiovascular Disease
Rahway, New Jersey, United States · Remote OK
$142k–$224k/yr
Job Description Our marketing teams are passionate about bringing our medicines and vaccines to the world. Through digital listening and patient analytics, we are able to understand our customers’ needs and strive to pro…
Skills: Account Management, Adaptability, Agile Principles, Brand Marketing, Business Relationship Building
Rahway, New Jersey, United States · Hybrid
$173k–$273k/yr
Job Description Responsible for managing external vendor(s)/partner(s) who provide resources and services that are critical to the success of Global Clinical Trial Operations (GCTO) and Global Clinical Development (GCD) …
Skills: Clinical Decision Making, Clinical Development, Clinical Technology, Clinical Trial Management, Conflict Resolution
North Wales, Pennsylvania, United States · Hybrid
$256k–$403k/yr
Job Description The Executive Director, Sales Force Effectiveness & Enablement, will report to the Associate Vice President, Field & Customer Excellence and serve as the enterprise leader for operational execution of Sal…
Skills: Account Management, Brand Management, Business Acumen, Business Planning, Cross-Functional Teamwork
Louisville, Kentucky, United States · Hybrid
$106k–$167k/yr
Job Description The Hospital / Institutional Customer Representative is a key member of the Hospital Customer Team and plays a critical role in supporting our Company's customer centric business model. He/she is responsi…
Skills: Account Management, Account Planning, Biopharmaceutical Industry, Customer Strategy, Hospital Sales
Rahway, New Jersey, United States · Hybrid
$157k–$247k/yr
Job Description This role will reside within the DHH US Market Engagement Team for Pharma. This team provided strategic thought-partnership to US commercial stakeholders through understanding brand strategy, co-creating …
Skills: Brand Strategy, Business Analysis, Commercial Analytics, Data Science, Natural Language Processing
Rahway, New Jersey, United States · On-site
$142k–$224k/yr
Job Description Our marketing teams are passionate about bringing our medicines and vaccines to the world. Through digital listening and patient analytics, we are able to understand our customers’ needs and strive to pro…
Skills: Payer Marketing, Market Access, Pricing Strategies, Brand Marketing, Account Management
North Wales, Pennsylvania, United States · On-site
Summary: The Plant Manager is responsible for the day-to-day operations of the entire manufacturing facility including safety, quality, efficiencies and meeting customer expectations. This includes driving strategic plan…
Skills: Plant Management, Lean Manufacturing, Six Sigma, P&L Management, Strategic Planning
Rahway, New Jersey, United States · Hybrid
$142k–$224k/yr
Job Description We are seeking a highly motivated, collaborative, and outcomes-driven leader to join our company’s Digital Human Health (DHH) organization and play an active role in our company’s Human Health transformat…
Skills: Asset Management, Backlog Management, Benefits Management, Biopharmaceutical Industry, Business Partnerships
Rahway, New Jersey, United States · Hybrid
$311k–$489k/yr
Job Description Global Clinical Trial Operations (GCTO) is a global organization with approximately 10,000 staff operating in 50 countries. The Program and Study Management organization (PSM) is a sub-functional unit wit…
Skills: Change Management, Clinical Development, Clinical Risk Management, Clinical Trial Management, Clinical Trial Methodology
Rahway, New Jersey, United States · Hybrid
$311k–$489k/yr
Job Description Global Clinical Trial Operations (GCTO) is a global organization with approximately 10,000 staff operating in 50 countries. The Program and Study Management organization (PSM) is a sub-functional unit wit…
Skills: Change Management, Clinical Development, Clinical Risk Management, Clinical Trial Management, Clinical Trial Methodology
Rahway, New Jersey, United States · Remote OK
$256k–$403k/yr
Job Description Our US Ophthalmology team is committed to transforming the lives of patients living with diabetic macular edema (DME) and neovascular age-related macular degeneration (nAMD) with a portfolio of two produc…
Skills: Advertising Campaign Development, Biopharmaceutical Industry, Brand Management, Brand Marketing, Content Creation
North Wales, Pennsylvania, United States · Remote OK
$191k–$300k/yr
Job Description Role Summary: The HIV Global Scientific Training (GST) Director position resides in the Global Medical & Value Capabilities organization within Value & Implementation (V&I), which also includes Global Med…
Skills: Adaptability, Adult Learning Theory, Business Acumen, Clinical Development, Cross-Functional Teamwork
North Wales, Pennsylvania, United States · Remote OK
$191k–$300k/yr
Job Description We are seeking a Growth and Improvement minded Regional Medical Scientific Director (aka Medical Science Liaison, MSL) in Inflammatory Bowel Disease Immunology that can help drive our Strategic Operating …
Skills: Clinical Trials, External Collaboration, Immunology, Immunotherapy, Inflammatory Bowel Diseases
Rahway, New Jersey, United States · Hybrid
$311k–$489k/yr
Job Description Global Clinical Trial Operations (GCTO) is a global organization with approximately 10,000 employees operating in 50 countries. The Program and Study Management organization (PSM) is a sub-functional unit…
Skills: Change Management, Clinical Development, Clinical Risk Management, Clinical Trial Management, Clinical Trial Methodology
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Lead the authoring, editing, and review of compliant clinical and regulatory documents and public-facing materials across multiple therapeutic areas. Provide program oversight, mentor other medical writers, and drive initiatives to improve medical writing processes and standards.
Requires a Bachelor's degree in a scientific or health discipline and at least 5 years of relevant medical writing or industry experience. Candidates must demonstrate expertise in managing complex writing projects, interpreting clinical data, and leading cross-functional teams.
The Clinical and Regulatory Strategic Communications (CRSC) department within GCTO creates and delivers high-quality regulated content in support of our development pipeline and enables data sharing for our customers. We are a strategic partner that ensures excellence and compliance with applicable laws while incorporating health literacy principles in the development of public-facing materials.
The Principal Medical Writer, Disclosure, in partnership with a project lead, leverages strategic and scientific expertise to develop, author, edit, and lead the review of accurate, clear, and compliant clinical, regulatory, and/or public‑facing documents, across multiple programs and therapeutic areas, in support of the company portfolio.
Is recognized as a subject matter expert in the design, planning, authoring, editing, and review of accurate, clear, high-quality documents that reflect applicable medical writing best practices (e.g., lean writing, health literacy) and evolving regulatory requirements.
Is recognized as a strong scientific contributor and collaborator on cross-functional teams and demonstrates an understanding of team and project leadership responsibilities.
Applies critical thinking, problem solving, and negotiation skills to implement innovative solutions to complex challenges across the medical writing scope of work (e.g., documents, content, processes, timelines, tools) while navigating project team dynamics.
Provides program oversight by keeping project leads and/or management informed and escalates, as needed, issues that could impact timelines, quality, or compliance.
Demonstrates expertise in medical writing-specific tools and technology platforms.
Leads initiatives to improve medical writing processes and standards; may serve as a resource for this work internally and externally, as appropriate.
Applies in-depth knowledge of clinical development, relevant regulations, disease areas, and company products. Demonstrates a developing understanding of the pharmaceutical industry beyond clinical research.
Provides scientific and operational mentorship, coaching and/or project oversight to support other medical writers.
May manage direct reports including workload, professional development, and performance management.
Required: Bachelor’s degree or higher preferably in a health, scientific, or relevant discipline (e.g., life sciences, pharmacy, medicine, public health) and at least 5 years of relevant medical writing or industry experience.
Experience managing complex writing projects in a deadline-driven environment and leading teams of medical writers and/or cross-functional team members.
Ability to critically evaluate and interpret clinical data clearly, objectively, and in accordance with regulatory requirements and industry guidelines.
Demonstrated critical thinking and problem-solving capabilities, with an ability to innovate, influence, and drive change.
Demonstrated effective leadership across organizational levels, including conflict resolution, negotiation, navigating teams through ambiguity, and decision making.
Excellent oral and written communication and presentation skills.
Technical expertise in commonly used office applications (e.g., Microsoft Office Suite) shared document systems (e.g., SharePoint) and willingness to learn and adapt to emerging technology.
Experience independently authoring scientifically valid public disclosure postings in accordance with global and local disclosure regulations.
Knowledge of disclosure regulatory intelligence and evolving industry trends to assess impact on business activities.
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Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process.
As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:
We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.
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The salary range for this role is
$142,400.00 - $224,100.00This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.
The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.
We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits.
You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.
San Francisco Residents Only: We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance
Los Angeles Residents Only: We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance
Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, 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.
Travel Requirements:
10%*A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
At MSD, known as Merck & Co., Inc., Rahway, NJ, USA in the United States and Canada, we are unified around our purpose: We use the power of leading-edge science to save and improve lives around the world. For more than 130 years, we have brought hope to humanity through the development of important medicines and vaccines. We aspire to be the premier research-intensive biopharmaceutical company in the world – and today, we are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. We foster a diverse and inclusive global workforce and operate responsibly every day to enable a safe, sustainable and healthy future for all people and communities. For more information, visit www.msd.com and connect with us on Facebook, Instagram, Twitter, and YouTube.
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Based on 156 listings with disclosed salaries, most management & leadership jobs in North Wales, PA pay between $129k–$300k per year. Individual offers vary with seniority, company size, and specialization.
There are currently 183 open management & leadership positions in North Wales, PA listed on Clera. New openings are added daily as companies post roles.
Companies currently hiring include MSD, Mission Critical Group, Gwynedd Manufacturing Inc., Helping Hands Family - Autism Services, Residence Inn by Marriott, among others. Browse the listings above to see every active employer.
Yes — 130 of the 183 open management & leadership positions offer remote or hybrid work (28 remote, 102 hybrid).
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.
