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Clinical Research Scientist Job Opening at Strand Life Sciences For Freshers

Job highlights

Work/Life Balance

Time management

challenging projects

Insurance

Are you a passionate life sciences professional looking to kickstart or advance your career in clinical research? Strand Life Sciences, a renowned name in the field of genomics and clinical research, is hiring for the position of Clinical Research Scientist in Bengaluru. This is an excellent opportunity for candidates with a Ph.D. in Life Sciences and 0-2 years of experience to work on cutting-edge projects in oncology, reproductive health, metabolic disorders, and neurodegenerative diseases. Read on to learn more about this exciting role and how to apply.

As a Clinical Research Scientist at Strand Life Sciences, you will play a pivotal role in planning, implementing, and executing clinical trials. Your responsibilities will include:

  1. Scoping and Feasibility Analysis:
    • Conduct feasibility analysis for upcoming projects in areas like oncology, reproductive health, and metabolic disorders.
    • Engage with investigators to estimate recruitment rates and design studies involving genomics components.
  2. Planning and Setup:
    • Draft and refine study-related documents and EC dossiers.
    • Identify and shortlist candidate sites, negotiate agreements, and ensure timely EC approvals.
    • Perform quality control (QC) checks on clinical data to ensure accuracy and compliance.
    • Set up systems like IVRS/IWRS, EDC for electronic CRFs, and manage regulatory submissions (DCGI/CTRI/HMSC).
  3. Implementation and Execution:
    • Train site staff and conduct site initiation activities.
    • Ensure adherence to GCP guidelines and manage SAE reporting.
    • Troubleshoot recruitment challenges and ensure smooth trial execution.
    • Maintain study records for audits and regulatory inspections.

Candidate Requirements
To be considered for this role, you should meet the following criteria:

  • Educational Qualification: Ph.D. in Life Sciences.
  • Experience: 0-2 years in oncology or clinical trials management.
  • Skills:
    • Strong understanding of clinical trial methodology, GCP, and GDMP.
    • Knowledge of NDCT rules, ICMR guidelines, and DCA.
    • Proficiency in clinical data management and electronic data capture systems.
    • Excellent organizational, analytical, and communication skills.
  • Other Requirements:
    • Willingness to travel (50% or more) and work in multicultural environments.
    • High attention to detail and a flexible, scientifically curious mindset.

Why Join Strand Life Sciences?
Strand Life Sciences is a leader in genomics and clinical research, offering a dynamic work environment where innovation and collaboration thrive. By joining their team, you will:

  • Work on groundbreaking projects in diverse therapeutic areas.
  • Gain hands-on experience in clinical trial management and regulatory compliance.
  • Be part of a multicultural and multidisciplinary team.
  • Enjoy opportunities for professional growth and development.

Application Link

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