Beijing, Beijing, China · On-site
Job Description Responsibilities include but are not limited to: Main responsibilities involve study level project management support which includes the following activities: Responsible for operational planning and proj…
Skills: Project Management, Epidemiology, Clinical Research, Observational Research, Data Management
Rahway, New Jersey, United States · Hybrid
$191k–$300k/yr
Job Description We are seeking an experienced talented scientist to join the Quantitative Pharmacology and Pharmacometrics – Immune/Oncology (QP2-IO) team in the role of Director. QP2-IO team is part of the Global Clinic…
Skills: Clinical Pharmacology, Pharmacometrics, Oncology, Drug Development, Data Modeling
Singapore, Singapore · On-site
Job Description About: In this role, you will support the site energy sustainability program and introduce good energy management practices to improve energy efficiency and reduce environmental impact. The program shall …
Skills: Energy Management, Energy Efficiency, Data Analysis, Project Management, Engineering Standards
Petaling Jaya, Selangor, Malaysia · Hybrid
Job Description Senior Specialist Talent Acquisition Scale shared service hiring. Drive regional talent impact across APAC Shape regional hiring impact from Malaysia — partnering across APAC to deliver critical talent fo…
Skills: Talent Acquisition, Stakeholder Management, Recruitment Strategy, Shared Services, Market Mapping
Prague, Prague, Czechia · Hybrid
Job Description Human Resources Specialist At our company, we aspire to be the premier research-intensive biopharmaceutical company. We're at the forefront of research to deliver innovative health solutions that advance …
Skills: HR Generalist, HR Operations, Czech labor legislation, Workday, HR data reporting
Lucerne, Lucerne, Switzerland · Hybrid
Job Description The Director in Global Clinical Supply (GCS) Compliance is a technical leader responsible for governing and advancing GCS’s global GxP Quality Systems to ensure the organization executes clinical supply o…
Skills: Compliance Strategies, Gmp Compliance, Lean Six Sigma, Performance Monitoring, Process Improvements
Mumbai, Maharashtra, India · Hybrid
Job Description Senior Manager Marketing (Oncology) Overview: The Senior Manager Marketing (Oncology) will support in conceptualization and implementation of marketing strategies for our oncology portfolio. This role wil…
Skills: Oncology Marketing, Brand Management, Marketing Strategy, Project Management, Data Analysis
Buenos Aires, Argentina · Hybrid
Job Description The position is part of the local Finance team for the region comprising Argentina, Uruguay, and Paraguay. In this role, the selected candidate will be responsible for ensuring the accurate recording, rec…
Skills: Financial Accounting, Reconciliation, Month-end Close, Financial Reporting, Audit Support
Upper Gwynedd Township, Pennsylvania, United States · On-site
$142k–$224k/yr
Job Description The Analytical Enabling Capabilities organization in West Point, PA is seeking a motivated scientist with technical expertise in mass spectrometry-based protein, protein conjugation or oligonucleotides or…
Skills: Mass spectrometry, Analytical chemistry, Vaccine development, Proteomics, LC-MS
Rahway, New Jersey, United States · Hybrid
$157k–$247k/yr
Job Description Our company is a global healthcare leader with a diversified portfolio of prescription medicines, vaccines, and animal health products. We are recognized as an industry leader in immuno-oncology (IO) and …
Skills: Clinical Development, Clinical Pharmacology, Communication, Data Modeling, Dose Response Analysis
Bogota, Capital District, RAP (Especial) Central, Colombia · Hybrid
Job Description The Senior Scientist, Clinical Safety Scientist (CSS) supports safety reporting for clinical trials across multiple therapeutic areas and investigational product development programs, from early- through …
Skills: Drug Safety, Clinical Trials, Pharmacovigilance, Good Clinical Practice (GCP), Clinical Development
Rahway, New Jersey, United States · Remote OK
$191k–$300k/yr
Job Description Director/Principal Scientist, Devices and Drug-Device Combinations Regulatory CMC Reporting to the Director of Device Regulatory Affairs for Autoinjector Development Programs, the Director/Principal Scien…
Skills: Regulatory CMC, Drug-device combinations, Autoinjector development, Inhalation delivery systems, Technical writing
Rahway, New Jersey, United States · Hybrid
$173k–$273k/yr
Job Description The Regulatory Affairs Headquarters Principal Scientist is responsible for development and implementation of global regulatory strategy for their assigned projects in the Vaccines and Infectious Disease t…
Skills: Regulatory strategy, Drug development, Clinical safety, Regulatory affairs, Vaccines
Boxmeer, North Brabant, Netherlands · On-site
Job Description Heb jij altijd al willen werken in een bedrijf waar je werk echt impact kan hebben? Werk je graag in een internationale omgeving met veel ruimte voor persoonlijke groei en ontwikkeling? Wij zijn in voor o…
Skills: Leadership, Good Manufacturing Practices (GMP), Problem Resolution, Process Improvements, Production Planning
Lidköping, Västra Götaland County, Sweden · Hybrid
Job Description Om rollen Som Technology Aftersales Support Tier 1 har du en central och synlig roll i vår kundupplevelse. Du är ofta kundens första kontakt och en nyckelfigur i att skapa förtroende, snabb hjälp och lång…
Skills: Customer Service, Technical Support, CRM Software, SAP, Animal Husbandry
Unterschleißheim, Bavaria, Germany · On-site
Job Description Für unseren Produktionsstandort in Unterschleißheim suchen wir eine erfahrene Führungspersönlichkeit (m/f/d) für die Leitung unserer Bereiche Verpackung und Visuelle Inspektion. In dieser verantwortungsvo…
Skills: People Leadership, Good Manufacturing Practices (GMP), Pharmaceutical Manufacturing, Packaging Processes, Continuous Process Improvement
Warsaw, Masovian Voivodeship, Poland · Hybrid
Job Description The Associate Director, Data Architect (M-track) leads and develops a programming and reporting team - set goals, assign work, coach performance, and manage recruiting/onboarding - while communicating sta…
Skills: Data Analysis, Data Engineering, Data Validation, Electronic Data Capture (EDC), Good Clinical Practice (GCP)
Hong Kong, China · On-site
Job Description The Pharmacy Internship Training Programme will be conducted under the supervision of the Regulatory Affairs Team for graduates of local accredited Bachelor of Pharmacy ("BPharm") Programs offered by The …
Skills: Regulatory Affairs, Pharmacovigilance, Adverse Event Reporting, Regulatory Compliance, Strategic Planning
okres Praha-východ, Central Bohemian Region, Czechia · Hybrid
Job Description As a Platform Engineer you will design, deploy, and maintain data platforms, predominantly concentrating on Data Quality Platform. This role involves both creative and analytical skills to solve complex p…
Skills: SQL, Databricks, Python, GitHub, CI/CD
Dundalk, Leinster, Ireland · Hybrid
Job Description Join a state-of-the-art vaccines manufacturing facility in Dundalk and become a key member of the Digital Manufacturing Operations team. This role offers the opportunity to support and enhance critical ma…
Skills: Automation, Siemens TIA, iFIX, Industrial Automation, System Troubleshooting
Sign up with Clera and we'll reach out the moment a role actually fits you — no more spraying applications into the void.
The Associate Manager is responsible for the operational planning and project management of epidemiology research studies, including budget oversight and vendor management. They also ensure regulatory compliance, manage study documentation, and coordinate with cross-functional teams to maintain data integrity.
Candidates must hold a Master's degree in Public Health or a closely related discipline and possess at least three years of experience in clinical or observational research. Strong project management skills, lab management experience, and the ability to collaborate effectively with diverse stakeholders are required.
Job Description
Main responsibilities involve study level project management support which includes the following activities:
Current Employees apply HERE
Current Contingent Workers apply HERE
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:
No Travel Required*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.
Offices: 90 E Scott Ave, Rahway, New Jersey 07065, US · 2000 Galloping Hill Road, Kenilworth, NJ 07033, US · Jalan Puteri 5/20, Puchong, Selangor 47100, MY · Clos du Lynx 5, Woluwe-Saint-Lambert, Brussels Region 1200, BE · Keilaranta 3, Espoo, Southern Finland 02150, FI
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.
Offices: 90 E Scott Ave, Rahway, New Jersey 07065, US · 2000 Galloping Hill Road, Kenilworth, NJ 07033, US · Jalan Puteri 5/20, Puchong, Selangor 47100, MY · Clos du Lynx 5, Woluwe-Saint-Lambert, Brussels Region 1200, BE · Keilaranta 3, Espoo, Southern Finland 02150, FI
