Clinical Research Associate II

New

Skills

Clinical trial management Data management Good Clinical Practice (GCP) Interpersonal communication Patient recruitment Problem-solving Regulatory compliance Site monitoring Statistical analysis Time management

The Clinical Research Associate II will undergo training in site monitoring services for clinical studies conducted in Poland. This role involves ensuring that site management activities are performed effectively and comply with regulatory standards under the supervision of senior staff.

Key Responsibilities
  • Oversee site management activities for clinical studies.
  • Ensure compliance with regulatory requirements.
  • Assist in the training of site personnel.
  • Participate in monitoring visits and audits.
  • Report findings and recommendations to supervisors.
Required Skills & Qualifications
  • Bachelor's degree in life sciences or related field.
  • Understanding of clinical trial processes and regulations.
  • Strong organizational and multitasking skills.
  • Excellent communication and interpersonal abilities.
  • Proficiency in data management and reporting.

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Job Type: Remote

Salary: Not Disclosed

Experience: Entry

Duration: Months

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