Provides medical oversight of clinical trials
Attends and presents at investigator and sponsor meetings
Provides medical consultation to clients, investigators, and project team members
Monitors safety variables of clinical studies
Reviews adverse events of special interest
Contributes to departmental process improvement initiatives
Assists in writing/review of regulatory documents

Requirements

MD required with specialization/formal training in Oncology or Hemato-Oncology
at least one of the following:
Clinical experience in treating patients (comparable to 2 years)
Clinical trial experience in a CRO or pharmaceutical company (comparable to 1-2 years)
Direct experience in safety/Pharmacovigilance medical monitoring (comparable to 2 years)
Therapeutic expertise in medical specialty (Oncology or Hemato-Oncology)
Excellent interpersonal skills
Understanding of guidelines (FDA, ICH, EMA, GCP)
Working knowledge of biostatistics, data management, and clinical operations
Proficiency with relevant safety databases (e.g. MedDRA)
Fluency in spoken and written English

Benefits

competitive remuneration
annual incentive plan bonus
healthcare
range of employee benefits

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard skills

clinical trial experiencesafety monitoringPharmacovigilancebiostatisticsdata managementclinical operationsregulatory document writingadverse event reviewmedical consultationprocess improvement

Soft skills

interpersonal skillscommunication skills

Certifications

MDOncology specializationHemato-Oncology specialization