(Snr) Clinical Research Associate

Posted about 1 month agoViewed

💎 Seniority level: Senior, 1+ years

📍 Location: Australia

🔍 Industry: Clinical Research Organization

🏢 Company: Precision Medicine Group👥 1001-5000💰 $35,160,000 about 4 years agoPharmaceutical Biotechnology Medical Precision Medicine Health Care

🗣️ Languages: English

⏳ Experience: 1+ years

🪄 Skills: Project CoordinationCommunication SkillsAnalytical SkillsProblem SolvingAttention to detailTime ManagementWritten communicationMS OfficeReportingTraining

Requirements:

Life science degree and / or equivalent experience
CRA experience within the CRO or pharmaceutical industry (and working in Oncology).
Minimum of 1 year experience as a CRA in Oncology
Availability for domestic travel including overnight stays, as required (international travel may be required for some senior level positions)

Responsibilities:

Monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards.
Coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.).
Train and mentor junior staff members (for Senior CRAs)
Interact directly with clients, initiate payments, and participate in proposal activities, including development and client presentations (for Senior CRAs)

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🔥 (Snr) Clinical Research Associate

Posted about 1 month ago

📍 Australia

🧭 Full-Time

🔍 Clinical Research

🏢 Company: Precision for Medicine

🔧 Requirements

Life science degree and / or equivalent experience
CRA experience within the CRO or pharmaceutical industry (and working in Oncology). We require a minimum of 1 year experience as a CRA in Oncology, and can offer CRA II and Senior CRA titles depending on experience level.
Availability for domestic travel including overnight stays, as required (international travel may be required for some senior level positions)

💡 Responsibilities

Monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards.
Coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.).
Support Project Managers with trials that are larger in scope.
Train and mentor junior staff members.
Interact directly with clients, initiate payments, and participate in proposal activities, including development and client presentations.

Project ManagementCommunication SkillsAnalytical SkillsProblem SolvingMentoringAttention to detailWritten communication

Posted about 1 month ago

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