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Apotex Hiring Senior Clinical Research Associate Job

Apotex Hiring Senior Clinical Research Associate Job contract role in Bangalore. Apply CRA jobs with bioequivalence study and global pharma exposure.


Company Overview

Apotex is a globally recognized pharmaceutical company headquartered in Canada, known for its strong presence in generic medicines, biosimilars, and specialty pharmaceuticals. Since its establishment in 1974, the company has expanded operations across multiple continents and now serves healthcare markets in over 100 countries.

Apotex Research Private Limited (ARPL), the company’s Indian R&D arm based in Bangalore, plays a crucial role in product development, bioequivalence studies, clinical research, and analytical support. With approvals from major global regulatory authorities such as US FDA, MHRA, TGA, and WHO, ARPL offers an excellent platform for clinical research professionals seeking global exposure. Apotex Hiring Senior Clinical Research Associate Job


Job Location & Employment Type

  • Location: Bangalore, India
  • Employment Type: Contract Role
  • Department: Clinical Research / Clinical Operations
  • Experience Required: 3–6 years

Open Position

Senior Clinical Research Associate (Contract)

Function: Clinical Operations / Bioequivalence Studies

This role focuses on execution and coordination of clinical and bioequivalence studies in compliance with regulatory guidelines and internal SOPs. It is ideal for experienced CRAs looking for hands-on clinical operations exposure in regulated environments. Apotex Hiring Senior Clinical Research Associate Job


Key Roles & Responsibilities

The Senior CRA will oversee operational aspects of clinical studies while ensuring adherence to GCP, regulatory requirements, and internal quality standards. Apotex Hiring Senior Clinical Research Associate Job

Study Execution & Coordination

  • Conduct clinical study activities as per approved protocols and SOPs.
  • Coordinate with investigators and study coordinators for smooth study execution.
  • Support protocol training and study initiation activities.
  • Plan and oversee subject check-in processes and clinical operations.
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Study Documentation & Compliance

  • Prepare and maintain Trial Master File (TMF) documentation.
  • Compile raw data, study schedules, and operational documents.
  • Ensure all documentation meets regulatory and audit requirements.
  • Assist in preparation and compilation of clinical study reports.

Clinical Operations Oversight

  • Ensure clinical site activities comply with protocol and SOP requirements.
  • Monitor study progress and review data for completeness and accuracy.
  • Support dosing-related activities and clinical study procedures.
  • Oversee study material management and accountability.

Data Handling & Reporting

  • Upload and manage study forms within internal systems.
  • Review subject documents such as informed consent forms and logs.
  • Prepare periodic study updates and status reports.
  • Assist in clinical report preparation and documentation review.

Study Close-Out Activities

  • Support sample transfer coordination with relevant teams.
  • Compile case report forms and study documentation.
  • Assist in archival and closure of study files.
  • Participate in document formatting and submission readiness.

Cross-Functional Collaboration

  • Work closely with investigators, coordinators, and operations teams.
  • Ensure subject safety monitoring and follow-ups.
  • Support clinical operations leadership with additional study tasks.
  • Maintain adherence to company ethics, quality, and safety policies.

Apotex Hiring Senior Clinical Research Associate Job


Eligibility Criteria

Education

  • B.Pharm or M.Pharm (mandatory)

Candidates with clinical research certifications will have an advantage.


Experience

  • 3–6 years of experience in:
    • Clinical operations
    • Bioequivalence studies
    • Clinical trial execution

Experience in regulated environments is strongly preferred.


Skills Required

  • Strong understanding of GCP and clinical research guidelines.
  • Hands-on experience in clinical trial operations.
  • Knowledge of bioequivalence study workflows.
  • Familiarity with clinical documentation and TMF management.
  • Good communication and coordination skills.
  • Ability to manage multiple clinical activities simultaneously.
  • Strong compliance and quality mindset.
  • Flexibility to work in dynamic clinical environments.
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Salary & Benefits

  • Salary Range: ₹3 – ₹6 LPA (as per job listing)
    Additional benefits may include:
  • Exposure to regulated global clinical trials
  • Opportunity to work in a reputed multinational pharma company
  • Strong hands-on experience in clinical operations
  • Learning opportunities within bioequivalence research

Final compensation may vary based on experience and contract terms. Apotex Hiring Senior Clinical Research Associate Job


Selection Process

The recruitment process generally includes:

  1. Resume screening
  2. HR discussion
  3. Technical interview (clinical operations focus)
  4. Final selection round

The process may vary depending on project urgency.


How to Apply

Candidates can apply through the official job portal where the role is listed (platform-based application).
Ensure your CV highlights:

  • Clinical trial execution experience
  • Bioequivalence study exposure
  • GCP compliance knowledge
  • TMF and documentation handling

Apply Here


Important Dates

  • Application Deadline: Not specified

Candidates are advised to apply early due to limited openings.


Why Apply for This Pharma Job?

This Apotex contract opportunity is ideal for mid-level clinical research professionals seeking exposure to regulated bioequivalence studies. Key advantages include:

  • Work with a globally reputed pharmaceutical company
  • Exposure to international regulatory standards
  • Hands-on experience in clinical and BE study operations
  • Opportunity to strengthen CRA career profile
  • Experience within a US FDA-approved research environment

For CRAs looking to build experience in regulated clinical research settings, this role offers strong practical exposure. Apotex Hiring Senior Clinical Research Associate Job


Important Note / Disclaimer

IndiaPharmaJobs.in is an independent job information platform sharing verified pharma and clinical research job updates. We are not affiliated with Apotex or any hiring organization. Candidates should apply only through official platforms and verify details independently. Apotex Hiring Senior Clinical Research Associate Job

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Final Call-to-Action

If you have clinical operations experience and want to work with a globally recognized pharma company, this Apotex Senior CRA contract role is a strong opportunity. Apply early and advance your clinical research career with international exposure. Apotex Hiring Senior Clinical Research Associate Job


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