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Clinical Research Professional
2 semanas atrás
Clinical Research Associate II / Senior Clinical Research Associate (CRA)
">We are seeking a highly skilled and experienced Clinical Research Associate to join our team in conducting clinical trials.
The ideal candidate will have a strong understanding of Good Clinical Practice (GCP) guidelines, regulatory requirements, and clinical trial protocols.
Responsibilities will include:
Site management: responsible for ensuring the integrity of clinical trials at designated sites.
Monitoring: conducts on-site monitoring visits to ensure compliance with study protocols and regulations.
Communication: maintains open communication with site staff, investigators, and sponsors to resolve issues and address concerns.
Documentation: ensures accurate and timely documentation of all study-related activities.
Collaboration: works collaboratively with cross-functional teams to ensure successful completion of clinical trials.
University degree or certification in a related field (e.g., nursing, pharmacy, medical research).
A minimum of 2 years of experience in clinical research, preferably in a CRA role.
Strong knowledge of GCP guidelines, regulatory requirements, and clinical trial protocols.
Excellent communication, organizational, and problem-solving skills.
Ability to work independently and as part of a team.
Additional experience in clinical research, preferably in a CRA role.
Familiarity with electronic data capture systems and clinical trial management software.
Proficiency in Microsoft Office applications (Word, Excel, PowerPoint).
Competitive salary and benefits package.
Opportunities for professional growth and development.
Collaborative and dynamic work environment.
