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Research Subject Care Professional

2 weeks ago


Pune, Maharashtra, India beBeeClinical Full time ₹ 15,00,000 - ₹ 28,00,000

Clinical Operations Specialist

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We are seeking a proactive clinical professional to safeguard the wellbeing of research subjects and ensure all clinical procedures are executed with the highest standards of care and in full compliance with protocols and regulatory guidelines.

">Roles and Responsibilities">
  • ">
  • Safeguard the wellbeing of research subjects in a medical capacity, adhering to established guidelines and protocols.">
  • Review study protocols and execute procedures in alignment with protocols and regulatory, health, and safety standards.">
  • Recruit and coordinate communication with clinical trial volunteers and patients, maintaining clear and effective communication throughout the study.">
  • Follow all applicable regulations globally and by region, ensuring consistency and accuracy.">
  • Collaborate with cross-functional teams to develop study materials, including informed consent forms and study manuals.">
  • Monitor trial progress and address any issues that arise during the study, providing timely resolutions.">
  • Provide organizational support and assist with administrative tasks as needed, contributing to overall efficiency.">
  • Perform routine tasks with some deviation from standard practice, adapting to changing circumstances and prioritizing needs.">
  • Utilize broad knowledge of operational systems and practices to improve study processes and outcomes, driving continuous improvement.">
">Required Skills and Qualifications">
  • ">
  • A strong understanding of clinical research protocols and regulatory requirements, with a minimum of 2 years of experience in clinical operations or a related field.">
  • A high school diploma or equivalent is required; an Associate's degree or higher in a related field is preferred.">
  • Excellent communication and interpersonal skills, with the ability to work effectively in a team environment.">
  • Strong organizational and time management abilities, with attention to detail and accuracy in documentation.">
  • Proficiency in Microsoft Office Suite and clinical trial management software, with a Certified Clinical Research Coordinator (CCRC) or equivalent certification preferred.">
  • Basic Life Support (BLS) certification is required.">
"],