Responsibilities

Supports the operational aspects of procedural documentation creation, management and

advises on process documentation strategy for MercksGlobal Regulatory Affairs & Clinical Safety

(GRACS) organization within Merck Research Laboratories (MRL). The role is responsible

for GRACS enterprise-wide, centralized project management leadership and coordination supporting the

GRACS Business System Owners, Global Process Leads and Functional Areas in the development, revision,

implementation and maintenance of their procedural documentation (policies, standard operating procedures

and supporting documents) related to global Regulatory Affairs and/or Pharmacovigilance activities.

Conducts large and small-scale business impact a assessments while working key project stakeholders

and process owners to ensure project outcomes meet business and compliance requirements

The role collaborates with Global Process Leads, Business System Owners, Functional Leads,

Document Owners, and Subject Matter Experts (SMEs) to ensure the documentation conforms

to MRL standards for classification within a prescribed documentation hierarchy and adequately

reflects the intended processes to support GRACS business activities

Salary Range: $130,000 -$150,000 year

TCS Employee Benefits Summary:

Discretionary Annual Incentive.

Comprehensive Medical Coverage: Medical & Health, Dental & Vision, Disability Planning & Insurance, Pet Insurance Plans.

Family Support: Maternal & Parental Leaves.

Insurance Options: Auto & Home Insurance, Identity Theft Protection.

Convenience & Professional Growth: Commuter Benefits & Certification & amp; Training Reimbursement.

Time Off: Vacation, Time Off, Sick Leave & Holidays.

Legal & Financial Assistance: Legal Assistance, 401K Plan, Performance Bonus, College Fund, Student Loan Refinancing.

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