Job Description

• Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.
• We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.

Job Description

Responsibilities:

• Collect, enter, and manage clinical trial data using electronic data capture (EDC) systems.
• Perform data validation and query management to ensure data quality and compliance with study protocols.
• Assist in the development of case report forms (CRFs) and data management plans (DMPs).
• Conduct ongoing data review and discrepancy resolution in collaboration with clinical staff.
• Generate data listings and summaries for interim and final study reports.
• Ensure data handling is following GCP, ICH guidelines, and applicable regulatory requirements.
• Maintain study documentation, audit trails, and data queries logs.
• Participate in cross-functional study team meetings and contribute to project timelines.

Requirements:

• Bachelor's degree in life sciences, healthcare, information technology, or related field.
• 1–3 years of experience in clinical data management or a related clinical research role.
• Familiarity with EDC systems (e.g., Medidata Rave, Oracle Clinical, Redcap).
• Knowledge of GCP, ICH, and regulatory guidelines.
• Excellent attention to detail, organizational, and communication skills.
• Proficiency in Microsoft Excel and other data management tools.

Additional Information

All your information will be kept confidential according to EEO guidelines.

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