Labcorp Associate Reviewer Job For Life Sciences, Apply Online

Labcorp Associate Reviewer Job For Life Sciences, Apply Online

Labcorp Associate Reviewer Job For Life Sciences, Apply Online. Associate Jobs. Life Sciences Associate EDS Reviewer Vacancy. Interested and eligible applicants can check out all of the details on the same below –

Name of the Post – Associate EDS Reviewer

Location – Bangalore, India

Job ID – 81999

Job Overview –

• Follow applicable departmental Standard Operating Procedures and Work Instructions.
• Complete required training according to timelines.
• Review and action query on an ongoing basis and updates database appropriately in
  accordance with Global Data Management Plans and applicable standardized data
  management.
• Perform UAT according to Validation Plan for applicable Data Management systems (if
  applicable).
• Generate, resolve and track queries to address inconsistent data identified during data
  review activities and apply proper modification/correction to the database.
• Run ancillary programs (e.g., diagnostics, special listings, reconciliation discrepancy
  listings) used to support the review of clinical trial data.
• Review reports and take actions as defined in the DMP or eCRF review manual.
• Assist with the review of clinical data by patient, site and/or project to identify data
  inconsistencies that require further investigation.
• Involve in data management system edit/data validation checks and special listings /
  procedures used as tools for the data review and discrepancy management activities.
• Maintain Data Management related operational data flows.
• Ensure that all Data Management activities are conducted in compliance with relevant
  regulatory requirements.
• Other duties as assigned by study management.

Education/Qualifications –

• University/college degree (life sciences, health sciences, information technology or
  related subjects) or a certification in allied health professions from an appropriate
  accredited institution.
• Fluent in English, both written and verbal.

Experience –

• 2 years’ prior experience in the pharmaceutical, biotechnology, medical
  device/diagnostics, or clinical trial industries or an equivalent combination of education
  and experience to successfully perform the key responsibilities of the job.
• A basic understanding of medical terminology is a plus.
• Strong organizational, planning, and critical-thinking skills.
• Well-polished, inclusive, and engaging communication skills (written and verbal) to
  support effective interactions with sponsors and internal colleagues.
• Ability to handle multiple tasks in a timely and professional manner under demanding
  conditions.
• Ability to use standard Microsoft suite of software products.
• Strong technical aptitude.
• Ability to maintain the confidentiality of data and information during interaction with staff at all levels.
• Understanding of ICH-GCP principles.

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