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Impactful Clinical Research Job at Syngene, Bangalore | Apply for this Clinical Operations Career!

Clinical Research Job at Syngene, Bangalore

Looking to advance your career in clinical research and site management? This Senior Clinical Research Associate (Sr. CRA) role offers an excellent opportunity to work in clinical operations. You will be responsible for managing clinical trial sites and ensuring compliance with global standards. The Clinical Research Job at Syngene Careers in Bangalore involves monitoring studies, maintaining quality, and supporting research excellence. It is ideal for professionals with experience in clinical trials and regulatory processes. Join a leading research organization and contribute to impactful scientific advancements.

About the Company:

Syngene is an innovation-led contract research, development, and manufacturing organization. The company provides integrated scientific services from early discovery to commercial supply. With a strong focus on safety, quality, and integrity, Syngene supports global pharmaceutical and biotechnology companies in accelerating research and development.

Job Details:

  • Job Title: Senior Clinical Research Associate
  • Location: Bangalore
  • Department: Clinical Operations – T&CR
  • Division: Discovery Services
  • Job Type: Full-Time
  • Experience: Experienced Sr. CRA required

Key Responsibilities:

  • Perform site selection, initiation, monitoring, and close-out visits as a Clinical Research Associate
  • Manage assigned clinical trial sites, protocols, and therapeutic areas
  • Ensure compliance with Good Clinical Practice (GCP) guidelines
  • Conduct training for study protocols and site teams in this Clinical Research Job at Syngene Careers
  • Monitor subject recruitment, CRF completion, and data query resolution
  • Maintain study quality and integrity at the site level in this Clinical Research Job in Bangalore
  • Identify and resolve quality issues with the Clinical Project Manager
  • Prepare monitoring reports, documentation, and follow-up letters
  • Track regulatory and Ethics Committee submissions and approvals

Educational Requirements for this Job:

  • BAMS, BDS, MDS & BHMS
  • Relevant clinical research training and certifications preferred

Skills Required:

  • Strong communication and teamwork skills
  • Knowledge of GCP guidelines and clinical trial processes
  • Ability to work in dynamic and fast-paced environments
  • Strong organizational and time management skills
  • Problem-solving and analytical thinking
  • Ability to meet deadlines and manage multiple priorities
  • Attention to detail and a quality-focused mindset

Benefits of the Clinical Research Job:

  • Opportunity to work with a leading research organization
  • Exposure to global clinical trials and regulatory processes
  • Strong career growth in clinical research
  • Collaborative and safety-focused work environment
  • Learning and development opportunities
  • Equal opportunity and an inclusive workplace
  • Contribution to innovative drug development and healthcare advancements

CLICK HERE TO APPLY NOW

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