Senior IT Professional

2 days ago

Hyderabad Secunderabad Telangana, India beBeeIT Full time ₹ 1,04,000 - ₹ 1,30,878
Job Title: IT Manager - Clinical Study Teams

Our company is seeking an experienced IT Manager to join our Clinical Study Teams. As an IT Manager, you will be responsible for the efficient and consistent use of EDC systems, ensuring compliance with established procedures and standards.

Key Responsibilities:

  • Support clinical trial platform technologies.
  • Act as a data scientist, bringing awareness to patterns and analytical insight to support decision-making.
  • Coordinating and providing programming support to Clinical Study Teams.
  • Ensure efficient and consistent use of EDC system and ensure the use is complied with the established procedures or standards.
  • Acting as a technical point of contact for systems deliverables on defined programs.
  • Identify, recommend or implement system enhancements, new tools or emerging technologies to decrease database development cycle times and foster a collaborative working environment.
  • Providing technical and business process input / expertise on new and emerging technologies.
  • Develop, review and implement policies, SOPs and associated documents.
  • Ensure documentation supports CSAR operational or technical activities is in a complete manner and consistent with regulatory and the established processes.
  • Assist in preparing for and responding to audit findings (internal or external).

Requirements:

Education: Bachelor's degree or equivalent in life science, computer science, business administration or related discipline.

Experience: Specialist knowledge / experience in life sciences or a medically related field.

General biopharmaceutical clinical research experience (clinical research experience obtained working on clinical trials at a biotech, pharmaceutical or CRO company)

Skills:

  • Good Clinical Practice
  • Strong understanding and experience in the use of performance management techniques, measures, problem-solving and analytical thinking
  • Drug development and clinical trials processes
  • Data management processes
  • Clinical trial databases and applications
  • Study build and Edit check development
  • Programming Languages
  • Systems development lifecycle
  • Project planning and management
  • Collaborating with global cross-functional teams (team/matrix environment)
  • Quality management and Risk Analysis
  • Regulatory filings and inspections
  • Process improvement methodologies

PREFERRED QUALIFICATIONS:

Education: Advanced degree or equivalent in life science, computer science, math, statistics, business administration or related discipline with 9+ years of experience.

Experience: Broad knowledge / work experience in data management / programming in the Pharmaceutical or Biotech arena.

General project management and planning experience

Experience in oversight of outside vendors (CROs, central labs, imaging vendors, IRT vendors, etc.)

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