Freshers Pharma Jobs at Apotex – Apply Now!
Clinical Research Associate
Date: Nov 30, 2024
Location: Bangalore, KA, IN, 560099
Company: Apotex
About Apotex Inc.
Apotex Inc. is a Canadian-based global health company that produces high-quality, affordable medicines for patients around the world. Apotex employs almost 7,200 people worldwide in manufacturing, R&D, and commercial operations. Apotex medicines are accessible to patients in more than 75 countries globally. Through vertical integration, the Apotex group focuses on the development and sale of generic, biosimilar, and specialty products.
For more information, visit: www.apotex.com.
Job Summary
Responsible for execution of study and system-related activities as per the established Standard Operating Procedures (SOP), Good Clinical Practices (GCP), Good Laboratory Practices (GLP), and regulatory requirements.
Job Responsibilities
- Conducts duties following established Apotex Research Pvt. Ltd., Bioequivalence Center’s SOPs and in a manner consistent with regulatory guidelines, GCP requirements, and Safe Work Procedures.
- Enters study data into required formats or databases for report table preparation and CDISC datasets preparation.
- Performs the collection, recording, and retrieval of information; verifies the accuracy of the information and manages data storage and retrieval systems.
- Reviews report tables.
- Handles activities related to requisition, receiving, and accountability of forms for the study.
- Ensures department readiness for regulatory audits by following good documentation practices, GCP, and relevant SOPs.
- Organizes files and collects clinical data to be entered into databases or required formats.
- Assists in reconciliation of study data.
- Coordinates/communicates internally or with cross-functional departments for study-relevant activities.
- Performs study activities as per study-specific protocol requirements and other duties as assigned by the Clinical Operations Management/delegate.
- Handles (receiving, issuing, storage, etc.) of Clinical Study Materials in stores.
- Performs work in accordance with all established regulatory, compliance, and safety requirements.
- Works in a safe manner, collaborating as a team member to achieve all outcomes.
- Demonstrates behaviors that exhibit organizational values: Collaboration, Courage, Perseverance, and Passion.
- Ensures personal adherence to compliance programs, including the Global Business Ethics and Compliance Program, Global Quality policies and procedures, Safety and Environment policies, and HR policies.
- Performs all other relevant duties as assigned.
Job Requirements
Education:Â B.Pharm / Pharm D / B.Sc. in a life sciences-related field.
Knowledge, Skills, and Abilities:
- Proficient in MS Office.
- Good communication skills.
- Flexible to work.
Experience: 0–2 years in Clinical Research.
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