Associate Director, Global Clinical Data Standards Vocabulary Specialist

🔥 14 minutes ago

🏖️ New Jersey, Pennsylvania – Remote

🏖️ New Jersey – Remote 🔔 Pennsylvania – Remote

💵 $142.4k - $224.1k / year

⏰ Full Time

🟠 Senior

👨‍⚕️ Medical Director

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MSD

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1891

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

Biotechnology • Pharmaceuticals • Healthcare Insurance

MSD is a leading biopharmaceutical company known as Merck & Co. , Inc. in the United States, Canada, and Puerto Rico, and as MSD globally. The company focuses on scientific innovation to deliver medicines and vaccines for various health challenges, including oncology, vaccines, infectious diseases, and cardio-metabolic diseases. MSD operates multiple divisions, including Human Health, Animal Health, and Research & Development. With approximately 75,000 employees worldwide and a significant investment in research and development, MSD is committed to improving global health through its scientific advancements. Additionally, the company places a strong emphasis on diversity, inclusion, and corporate responsibility. MSD’s operations extend worldwide, offering opportunities in numerous regions and promoting diversity and innovation in all aspects of its business.

📋 Description

• work independently or collaboratively as a member of a team or successful leader • interact with staff across multiple company sites • mentor, guide and provide direction to junior staff • lead or participate in internal clinical data standards forums • support standards development teams and data governance reviews • engage in strategic and process improvement/design projects • contribute to industry forums and standards development teams • maintain knowledge of new technologies, clinical study data standards and regulatory requirements

🎯 Requirements

• 8 years’ work experience in pre-clinical/clinical research • minimum 2 years’ experience in data standards • strong emphasis on managing and applying CDISC Controlled Terminology • knowledge of clinical research-controlled terminology (i.e., MedDRA, WHODD, SNOMED) • understanding of various external data types (i.e., genetics, immunogenicity, PK/PD) • understanding of collection and terminology associated with questionnaires • understanding of lab values and the importance and maintenance of unit of measure conversions • knowledge of versioning and maintenance of controlled terminology • excellent communication/presentation skills • must have an innovative spirit and outstanding stakeholder management skills • ability to manage multiple projects

🏖️ Benefits

• medical, dental, vision healthcare and other insurance benefits (for employee and family) • retirement benefits, including 401(k) • paid holidays • vacation • compassionate and sick days