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:

• Investigate, maintain, and manage regulatory product certification claims data, databases, and documentation systems.
• Ensure accurate data entries and effective database management.
• Review technical documents to retrieve information with a high level of accuracy.
• Maintain clear, concise documentation, with experience in documentation control and coordination.
• Perform other duties and responsibilities as assigned.
• Engage in meaningful work that contributes to product safety and compliance.
• Collaborate with a diverse team of professionals.
• Enhance your skills in regulatory affairs and documentation management.

Requirements:

• The ideal candidate will have strong attention to detail, excellent communication skills, and the ability to work independently and collaboratively, which will align successfully in the organization.
• 5 years of experience in a similar position.
• Strong written and verbal communication skills.
• Advanced skills with Microsoft Excel, including an understanding of Macros, and proficiency in Microsoft Suite.
• Opportunity to work in a dynamic and supportive environment.
• Gain valuable experience in a growing industry.

Additional Information

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

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