Sr. Data Entry

Found in: Appcast Linkedin GBL C2 - 2 weeks ago

Rahway, United States Merck Full time

Note: This is a hybrid part-time role (20 hours/week) and the candidate needs to be onsite once a week.


Qualifications:

Education: At least 2 years in college

SKILLS: Strong proficiency with Microsoft Excel; able to speak and write English well.

• Strong interpersonal and communication skills.

• Ability to understand and implement regulatory regulations guidelines and company procedures.

• Proactive, pragmatic, flexible, service-minded, and able to work under (time) pressure.


Experience

• Level I- (0-3), Experience working with clinical study data, Familiarity with GCP (Good Clinical Practice), CRF (clinical Report Form), and EDC (Electronic Database Capture) system.

• Experiences with pharmaceutical regulatory guidance.


Role:

• Transcribe clinical study data from paper clinical trial CRF to Excel or EDC system.

• Support relevant activities of the data management and clinical teams including document scanning and filing wherever needed.


Responsibilities:

• Data entry with high accuracy.

• Supporting data managers with quality data and collaborating with clinical teams regarding data issues.

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