Senior Medical Operations Professional

1 week ago

Pune, Maharashtra, India beBeeClinicalOperations Full time
Clinical Operations Specialist Role

As a Clinical Operations Specialist, you will play a critical role in safeguarding the wellbeing of research subjects in a medical capacity. Your primary responsibility will be to ensure that all procedures are conducted with the highest standards of care and safety.

  • You will review study protocols and execute procedures in alignment with protocols and regulatory, health, and safety standards, ensuring compliance with all relevant guidelines and regulations.
  • Recruiting and coordinating communication with clinical trial volunteers and patients will be another key aspect of your role. You must maintain clear and effective communication throughout the study.
  • Following applicable regulations globally and by region is crucial. You will ensure that all activities are conducted in accordance with local and international standards.
  • You will collaborate with cross-functional teams to develop study materials, including informed consent forms, study manuals, and other essential documents.
  • Monitoring trial progress and addressing any issues that arise during the study is vital. You must ensure that all problems are promptly identified and resolved.
  • In addition to the above responsibilities, you will provide organizational-related support or service, typically under supervision. You will assist with administrative tasks and other support activities as needed.
  • You will perform routine tasks with some deviation from standard practice. Adaptability is key as you will need to adapt to changing circumstances and requirements as necessary.
  • Your broad knowledge of operational systems and practices gained through extensive experience and/or education will be invaluable. You will apply this knowledge to improve study processes and outcomes.
Qualifications
  • A High school diploma or equivalent is required for this role.
  • An Associate's degree or higher in a related field is preferred.
  • A minimum of 2 years of experience in clinical operations or a related field is necessary.
  • You must have a strong understanding of clinical research protocols and regulatory requirements.
Additional Requirements
  • Certified Clinical Research Coordinator (CCRC) or equivalent certification is preferred.
  • BASIC Life Support (BLS) certification is required.
Essential Skills
  • Excellent communication and interpersonal skills are a must.
  • Strong organizational and time management abilities are essential.
  • Attention to detail and accuracy in documentation are crucial.
  • You must be able to work effectively in a team environment.
  • Proficiency in Microsoft Office Suite and clinical trial management software is necessary.

We value innovative professionals who can bring their expertise to our company. If you are interested in joining us, we would love to hear from you

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