Clinical Data Management Intern: Trial Planning & Quality

Merck; Rahway (NJ); Hybrid; USD 40,000 - 111,000; Full time

Benefits offered by this job

Hybrid work arrangement

Job summary

Merck Rahway, NJ invites applications for its Future Talent Program internship within the Research Lab Division. Internships last up to 12 weeks and include one or more projects, offering development and a potential long-term fit.

Role responsibilities include managing clinical data management activities for trials, developing project plans from protocol through database lock, coordinating with cross-functional teams, and ensuring data quality and timely deliverables.

Qualifications

• Candidate must be working towards completion of a B.A. or B.S. degree in life sciences, computer science or related discipline
• Candidates must be available to work full-time for up to twelve (12) weeks beginning June 2027
• Candidates must have interest in learning Clinical Data Management

Responsibilities

• Develops detailed project plans for collection, review, and cleaning of all clinical data for assigned trials.
• Serves as project manager of all clinical data management activities for trials as assigned.
• Project planning, initiation, execution, change control, and closing.
• Project team development, leadership, meeting management, and resource coordination.
• Risk management planning and escalation as necessary.
• Defines trial-level requirements for quality data collection and validation.
• Reads and interprets the clinical protocol from a clinical data management perspective.
• Engages with stakeholders to assess complexity and confirm data management deliverables.

Skills

Clinical Data Management

Project management

Communication skills

Leadership

Education

B.A./B.S. in life sciences or computer science

Tools

Database concepts and tools

Job description

Merck Rahway, NJ invites applications for its Future Talent Program internship within the Research Lab Division. Internships last up to 12 weeks and include one or more projects, offering development and a potential long-term fit.

Role responsibilities include managing clinical data management activities for trials, developing project plans from protocol through database lock, coordinating with cross-functional teams, and ensuring data quality and timely deliverables.