MSD Jr Data Engineer temporary 

Colombia 

68762869

Job Description

Our Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs, vaccines and new indications for existing products. We ensure we conduct high quality clinical trials by integrating state-of-the-art technology and applying rigorous scientific and ethical standards.

Requirements

: B.A. or B.S. degree, preferably in IT, mathematics, science, a healthcare-related discipline, or computer science; or relevant skills and experience.

Qualifications, Skills & Experience

• Knowledge of database structures and available tools to manage, extract, report, and warehouse data.
• Desirable knowledge of database structures and available tools to manage, extract, report, and warehouse data (SQL-PL/SQL scripting).
• Desirable 2 years of database development or data programming experience
• Desirable technical proficiency in a Clinical Data Management Systems (i.e., InForm, Inform Architect, Central Designer).
• 0-2 years’ experience in System Development Lifecycle Management / system validation knowledge.
• Desirable experience with reporting tools such as SAS, Cognos or JReview.
• Desirable experience in eCRF generation for site documentation and downstream regulatory compliance deliverables.
• Ability to collaborate and communicate with cross functional stakeholders to interpret and ensure quality report specifications and input to report development.
• Solid knowledge of MS Windows/Office software and exposure to web-based applications.
• Effective communication skills (oral and written) with the ability to communicate with both the technical and business areas.
• Strong organizational and critical thinking skills.
• Keen sense of urgency and customer focus.
• Ability to work cross functionally and as part of a team.
• Able to work independently, under pressure and change environment with flexibility.

• Creates and develops clinical databases and data transfer files according to written specifications.
• Participates in the review of electronic case report forms (eCRF) and edit checks, database development, programming of edit checks, and scripts to aid in transfer of electronic data files into the Clinical Data Management System (CDMS).
• Interface with members of study teams, including external CROs/Vendors where applicable, to integrate study team requirements into all deliverables.
• Responsible for reporting deliverables supporting data cleaning and verification and any external data captured in clinical studies.
• Creates and reviews reporting specifications to ensure high quality deliverables, meet SDTM structure requirements and the needs of the business.
• Participates in the review of standard and template reports, and scripts to aid in the review of data to ensure a quality database.
• Participate in database Archiving and Decommissioning activities in support of multiple clinical programs (with Vendors interaction).

• Interface with members of study teams and key stakeholders, to integrate requirements into all deliverables.
• Ensures adherence to clinical database standards, SDTM structures, SOPs, and Process Guidelines.
• Participates in activities including, but not limited to, task forces, testing of new systems and helps coordinate technical initiatives.

Current Contingent Workers apply

*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.

A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.