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Job Description
Responsibilities:
Develop strong site relationships and ensure continuity throughout all phases of the trial.
Perform clinical study site management activities in compliance with ICH-GCP, Sponsor SOPs, local laws & regulations, and protocol requirements.
Gain in-depth understanding of study protocols and related procedures.
Conduct remote and on-site monitoring activities to ensure data accuracy and subjects' safety.
Collect, review, and monitor regulatory documentation for study start-up, maintenance, and close-out.
Communicate with investigators and site staff on protocol conduct, recruitment, retention, and regulatory compliance.
Manage and maintain information and documentation in various systems.
Support audit and inspection activities as required.
Contribute to the identification and development of new potential sites.
Requirements:
Minimum 4 years of direct site management (monitoring) experience in bio/pharma/CRO.
Fluent in local languages and English (verbal and written) with excellent communication skills.
Excellent understanding of clinical research, GCP/ICH guidelines, and country-specific regulations.
Demonstrated ability to mentor and lead.
Strong IT skills and ability to adapt to new applications.
Ability to analyze data/metrics and take appropriate action.
Experience with site motivational visits to boost enrollment.
Capable of managing complex issues and implementing corrective action.
B.A./B.S. with strong emphasis in science and/or biology preferred.
Growth and development opportunities.
Competitive salary and benefits package.
Current Contingent Workers apply
*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.
Job Posting End Date:08/02/2024
A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
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