Clinical Research Physician

Benefits

Qualifications

• •Medical Doctor degree required
• •Excellent knowledge and understanding of oncology and oncology clinical trials
• •At least 1 year of experience in medical monitoring in oncology trials
• •Current knowledge of ICH GCP guidelines
• •Advanced proficiency in MS Office in Word, Excel, and PowerPoint
• •Strong teamwork abilities and communication skills
• •Excellent level of English is required
• •Spanish language knowledge will be valued
• •Must be legally authorized to work in the country
• •Salary to be influenced (or determined) by the education, experience, location, knowledge, skills, and abilities of the applicant, internal equity, and alignment with market data
• •Passion
• •Integrity
• •9 more items(s)

Responsibilities

• •Reporting to the Medical Monitoring Unit Manager, this will be a home-based, full-time position in the USA
• •Act as Medical Monitor, performing comprehensive medical monitoring activities
• •Respond to medical inquiries from investigational sites and trial teams
• •Review patient eligibility and protocol deviations
• •Oversee patient safety by reviewing medical data at patient and trial levels
• •Review Serious Adverse Events (SAEs), including coding, causality and expectedness assessments, and drafting company comments
• •Prepares scientific slides, attends and/or presents protocol information at Investigator Meetings, Scientific Committee meetings, Safety Review Committee meetings, SIVs, etc
• •Serve as the primary clinical point of contact for scientific questions from internal and external stakeholders (e.g., IRBs, sites, sponsor medical teams, trial teams)
• •Collaborates with the Medical Writing and Training Unit to write and/or review trial-specific medical documents (e.g., protocols, DSURs, CSRs)
• •Conducting medical training on selected trial-specific or non-trial-specific topics
• •7 more items(s)