Senior Data Specialist

Endpoint Clinical, Inc. · Other US Location

Company

Endpoint Clinical, Inc.

Location

Other US Location

Type

Full Time

Job Description

About Us:

Endpoint is an interactive response technology (IRT®) systems and solutions provider that supports the life sciences industry. Since 2009, we have been working with a single vision in mind, to help sponsors and pharmaceutical companies achieve clinical trial success. Our solutions, realized through the proprietary PULSE® platform, have proven to maximize the supply chain, minimize operational costs, and ensure timely and accurate patient dosing. Endpoint is headquartered in Wakefield, Massachusetts with offices across the United States, Europe, and Asia.

Position Overview:
The Senior Data Specialist will support all aspects of Data Management at Endpoint, including data changes, verifications, data transfers, and data integrations with supporting documentation. The person in this role will work independently with minimal guidance from management and will guide and mentor junior staff. The role requires interaction with internal study teams and occasionally with external end users and sponsors.


Responsibilities:

  • Drafts and executes quality SQL data scripts and queries for production data updates and reporting.
  • Manages data change request aspects of the endpoint eDRS system.
  • Reviews change requests for clarity, completeness, and impact.
  • Collaborates with Client Services and customers as needed to ensure database updates are made in the spirit of the original request.
  • Manages and continuously updates Data Management best practices.
  • Reviews Data Management Plan Specifications for quality, consistency, and feasibility.
  • Verifies database lock, project archives and client-related documents. 
  • Collaborates with IT and implementation team to address Clinical application requests and/or changes to Clinical database systems. 
  • Participates in conference calls and/or meetings with external teams as needed.
  • Performs other duties as required.
  • This position will require weekend and holiday coverage as needed.

Education:

  • Bachelor’s Degree or equivalent and/or appropriate experience

Experience:

  • 3-5 years of relevant experience with SQL data management, preferably in the clinical trials industry.
  • 2-3 years of experience in clinical trials industry.
  • Proven experience and expertise in SQL scripts, as well as creating complex queries and stored procedures.
  • Advanced MS Excel expertise; SAS is a plus.
  • Previous experience working in a fast-paced, entrepreneurial environment preferred.
  • Advanced knowledge of Microsoft Office applications (Outlook, Word, Excel, Visio, PowerPoint) and SQL.

Skills:

  • Proven ability to handle multiple tasks in a deadline-oriented production environment.
  • Ability to identify and solve technical problems independently.
  • Strong interpersonal skills with the ability to work effectively with a wide variety of professionals, both internal and external.
  • Strong collaboration skills.
  • Proactive team player enthusiastic with high work ethics.
  • Strong attention to detail and quality.
  • Excellent organizational and time management skills.
  • Excellent communication skills.

#LI-MT1 #LI-Onsite

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Date Posted

06/16/2024

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