Senior Clinical Trial Coordinator

2 days ago

Pune, Maharashtra, India beBeeClinical Full time ₹ 10,00,000 - ₹ 15,00,000

Clinical Trial Manager Job Summary

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We are seeking a highly skilled and experienced Clinical Trial Manager to join our team. The successful candidate will be responsible for the overall management of clinical trials, from planning and execution to closure.

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Key Responsibilities:

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  • Develop and coordinate Phase 1 clinical research studies, ensuring detailed planning and flawless execution.">
  • Implement clinical research protocols while ensuring compliance with Good Clinical Practice (GCP) and other regulatory requirements.">
  • Collaborate with principal investigators, research subjects, client teams, and clinic operations teams to ensure smooth study execution.">
  • Plan and manage logistics, scheduling, budgeting, and resource allocation for clinical trials.">
  • Track study progress against milestones, deliverables, and budgets, and provide regular updates to stakeholders.">
  • Prepare and present study reports, data analyses, and progress updates to clients and internal teams.">
  • Ensure adherence to global and regional regulations while staying updated with any regulatory changes.">
  • Provide guidance and mentorship to junior team members, fostering collaboration.">
  • Identify and resolve issues or risks during the study, ensuring timely corrective actions.">
  • Maintain comprehensive documentation of all study-related activities.">
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Qualifications:

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To be successful in this role, you will need:

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  • Bachelor's degree in Life Sciences, Clinical Research, or a related field.">
  • 3+ years of experience in clinical trial management or a related field.">
  • Strong knowledge of clinical research processes, GCP, and regulatory requirements.">
  • Proven project management and organizational skills.">
  • Excellent communication and interpersonal skills with ability to work independently and in teams.">
  • Proficiency with clinical trial management systems (CTMS) and tools.">
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Preferred Certifications:

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A Certified Clinical Research Professional (CCRP) certification or equivalent is preferred.

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Skills Required:

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To succeed in this role, you will need:

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  • Strong analytical and problem-solving abilities.">
  • High attention to detail and accuracy.">
  • Ability to manage multiple projects and priorities simultaneously.">
  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).">
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If you have the required skills and qualifications, please apply now

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