Join the world’s largest and most comprehensive clinical research organization, where healthcare intelligence drives innovation and continuous improvement. This is an opportunity for those looking to thrive in an environment that values diversity and empowers individuals to contribute meaningfully to saving lives.
Responsibilities:
- Conduct on-site monitoring of clinical trials.
- Prepare and submit documents to the Institutional Review Board (IRB).
- Manage responsible sites throughout the study lifecycle.
- Communicate directly with site staff and ensure compliance with study protocols.
- Collaborate with different stakeholders and vendors to facilitate trial success.
Qualifications:
- Education: B.Pharm, M.Pharm, Pharm D, BDS, or MBBS.
- Experience: Minimum of 1 year of onsite monitoring experience, specifically in Oncology (excluding any training or induction).
- Skills: Strong and clear communication skills are essential.
Application Process:
Interested candidates can apply through the designated portal or reach out to Sonia Oh for more information.
Remote Work: This position is eligible for remote work.
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