What are the responsibilities and job description for the Clinical Research Physician position at Lensa?
Lensa is a career site that helps job seekers find great jobs in the US. We are not a staffing firm or agency. Lensa does not hire directly for these jobs, but promotes jobs on LinkedIn on behalf of its direct clients, recruitment ad agencies, and marketing partners. Lensa partners with DirectEmployers to promote this job for Translational Research in Oncology. Clicking "Apply Now" or "Read more" on Lensa redirects you to the job board/employer site. Any information collected there is subject to their terms and privacy notice.
Translational Research in Oncology (TRIO)is a global academic clinical research organizationdedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing cancer treatments of the future to the world of today.
TRIO is looking for a Clinical Research Physician to join our Medical Monitoring Unit team. Reporting to the Medical Monitoring Unit Manager, this will be a home-based, full-time position in the USA.
Main Responsibilities
Prior to applying please review TRIO's Applicant Information Notice
Teamwork
If you have questions about this posting, please contact support@lensa.com
Translational Research in Oncology (TRIO)is a global academic clinical research organizationdedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is committed to providing cancer treatments of the future to the world of today.
TRIO is looking for a Clinical Research Physician to join our Medical Monitoring Unit team. Reporting to the Medical Monitoring Unit Manager, this will be a home-based, full-time position in the USA.
Main Responsibilities
- 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.
- 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 Officein 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
- Competitive Salary
- 3 weeks of vacation plus paid Christmas Closure
- 2 weeks paid personal/sick time
- 100% health benefits for you and your family paid by TRIO
- Flexible working hours
- Monthly internetallowance
- 401K Program 5% Salary Contribution
- Home office allowance
Prior to applying please review TRIO's Applicant Information Notice
Teamwork
- Passion
- Integrity
- Innovation
If you have questions about this posting, please contact support@lensa.com
Salary : $110,000 - $150,000