Clinical Operations & Documentation Coordinator II

Merck & Co.

Ridgefield (CT)

On-site

USD 52,000 - 76,000

Full time

7 days ago
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Job summary

Merck & Co. in Ridgefield, CT seeks a detail-oriented Coordinator to support Clinical Pharmacology and Safety Sciences (CPS) Central Function Office.

You will assist with operations, documentation management, and compliance activities, collaborating with CPS colleagues and external suppliers as needed. Responsibilities include handling inquiries by email, maintaining tracking spreadsheets and databases, processing documents, and ensuring timely delivery of administrative tasks while adhering to

Qualifications

  • Strong verbal and written communication skills.
  • Experience with admin operations and documentation.
  • Ability to manage multiple tasks with accuracy.
  • Familiarity with corporate compliance and policies.
  • Proficient in MS Office and SharePoint.

Responsibilities

  • Monitor and respond to inquiries received primarily through email, ensuring timely and professional communication.
  • Perform administrative activities in support of business operations, documentation management, and compliance.
  • Maintain departmental tracking spreadsheets, inventories, databases, and systems, including data entry and updates.
  • Execute document processing activities, including document creation, formatting, routing, and archiving.
  • Use various computer systems and tools to support established processes and workflows.
  • Follow applicable regulations, internal policies and procedures.
  • Collaborate with team members and stakeholders to support operational efficiency and timely completion of deliverables.

Skills

Strong communication
Organizational skills
Attention to detail
Team collaboration
Multitasking
Prioritization

Education

High school diploma
Business school certification or college degree preferred

Tools

Microsoft Word
Microsoft Excel
Outlook
SharePoint
Databases

Job description

Merck & Co. in Ridgefield, CT seeks a detail-oriented Coordinator to support Clinical Pharmacology and Safety Sciences (CPS) Central Function Office.

You will assist with operations, documentation management, and compliance activities, collaborating with CPS colleagues and external suppliers as needed. Responsibilities include handling inquiries by email, maintaining tracking spreadsheets and databases, processing documents, and ensuring timely delivery of administrative tasks while adhering to

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