Senior Clinical Programmer

☞ Clinipace

View: 108

Update day: 01-06-2024

Location: London

Category: R & D IT - Software

Industry: Biotechnology Pharmaceuticals Research

Position: Associate

Job type: Full-time

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Job content

Job Title:Senior Clinical Programmer

Job Location: High Wycombe, UK (Remote) Or any UK Remote Location

Clinipace (https://www.clinipace.com/) is a global, full-service contract research organization (CRO); our approach to clinical research is personal. We deliver a level of collaboration and flexibility not possible in a traditional CRO environment. Clinipace has an emphasis on personalized services and solutions, regulatory expertise, and therapeutic leadership. Our mission is to improve the way clinical research is performed in major therapeutic areas including oncology, rare disease, gastroenterology, nephrology, and women’s health. Clinipace strives to impact the future of drug development and health care by combining the most advanced technology and a CHALLENGE ACCEPTED approach. With offices in 23 countries and more than 850 professionals worldwide, our personalized services and solutions mean we are designed to face the most difficult industry challenges and guide our clients successfully through their clinical development programs.

Job Overview

The Senior Clinical Programmer (CP-Sr) supports clinical programming services. The CP-Sr creates, deploys, and maintains clinical databases and provides support to the study team as needed. The CP-Sr provides technical and functional expertise in EDC and IRT systems, and where appropriate, mentors and supports other staff and peers on clinical databases. Additionally, this role may provide input into protocols, budgets, contracts, and resource allocation at the request of the Clinical Programming leaders.

Job Duties And Responsibilities

The specific job duties of a Senior Clinical Programmer may include but are not limited to:
  • Design, manage, and maintain the clinical study database in keeping with the protocols and amendments, standard operating procedures (SOPs), good clinical practices (GCP), and other regulatory requirements.
  • Review system specifications and Data Validation Plan (DVP) and perform programming and configuration activities for assigned projects
  • Participate in release to production activities
  • Develop and implement validation procedures for clinical studies and their appropriate tests and documentation.
Supervisory Responsibilities

No supervisory responsibilities

Job Requirements

Education
  • Scientific, Informatics, Mathematics or Medical Documentation degree or equivalent combination of education and experience.
Experience
  • At least 5+ years of experience in design and deployment of clinical databases
  • C#, SQL, and/or custom function programming (preferred)
  • Medidata and/or Medrio configuration (preferred)
  • Knowledge of pharmaceutical industry and data standards (preferred)
  • Regular use of MS-Office, revision control system (e.g. Subversion), and issue tracking software (e.g. JIRA)
Skills/Competencies
  • Good problem solving abilities (technical, interpersonal, decision making)
  • Good communication skills (verbal and written)
  • Well organized and structured way of working
  • Devoted to high quality work and sound understanding of documentation needs
  • Ability to work in a team
  • Good working knowledge of database programming (e.g. Access, SQL, PL/SQL, XML)
  • Good understanding of medical and laboratory terminology
Capabilities
  • Ability to work remotely as applicable
  • High level of working time flexibility to adjust to project flows
The company will not accept unsolicited resumes from third party vendors.

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Deadline: 16-07-2024

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