Clinical Research Coordinator

2 weeks ago


Ahmedabad, Gujarat, India HOPS HEALTHCARE Full time

Job Summary:

HOPS HEALTHCARE is seeking a highly skilled Clinical Trials Specialist to join our team. In this role, you will be responsible for taking leadership to meet, collaborate and initiate clinical trials at various healthcare facilities. You will also prepare documentation for seeking permission to initiate clinical trials, manage healthcare facilities' requirements, needs, and help needed, and deliver results that have a direct impact on the successful completion of the clinical program.

Key Responsibilities:

  • Lead the planning and execution of clinical trials at healthcare facilities, ensuring timely and effective initiation and completion.
  • Develop and maintain relationships with healthcare facility staff, stakeholders, and other key partners to ensure successful trial execution.
  • Prepare and submit high-quality documentation for regulatory and institutional review board (IRB) approval, ensuring compliance with regulations and guidelines.
  • Collaborate with cross-functional teams to identify and mitigate risks, and develop contingency plans to ensure trial success.
  • Train and guide site staff in protocol and trial procedures to minimize protocol deviations (PDs) and ensure adherence to study protocols.
  • Monitor and review trial progress, identifying areas for improvement and implementing corrective actions as needed.
  • Collection and management of essential documents.
  • Team involvement and participation in meetings.

Requirements:

  • Bachelor's degree in a relevant field, such as biomedical engineering, nursing, or a related field.
  • Strong project management skills, with experience in managing multiple projects simultaneously.
  • Excellent communication and interpersonal skills, with the ability to work effectively with diverse stakeholders.
  • Ability to work independently and as part of a team, with a strong sense of accountability and responsibility.
  • Strong analytical and problem-solving skills, with the ability to identify and mitigate risks.
  • Experience with clinical trials regulations, guidelines, and best practices.


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