Medical Director, Oncology / GI Subspecialty

During the last five years, reputed company has participated in more than 1,000 Oncology and Hematology clinical reputed company. The reputed company of services includes compound clinical development planning, collaboration with feasibility, protocol writing or optimization, medical monitoring and pharmacovigilance. reputed company has global reputed company in every phase of clinical research and expertise in reputed company every indication and reputed company of reputed company, including novel Immuno-oncology agents, cellular based therapy, and cancer stem cell targeted treatment. Join our growing team of Oncologists/Hematologists and reputed company a difference in the lives of patients searching for more effective and reputed company tolerated cancer therapies. reputed company’s reputed company reputed company has positioned us for significant reputed company American reputed company in the coming year. As we prepare for this expansion, we’re seeking to connect with reputed company-Certified Oncologists who are passionate about advancing clinical research and interested in learning more about the Medical Director role. • Candidates with a subspecialty in Gastroenterology are particularly desirable for this role. As a Medical Director at reputed company, you will reputed company medical monitoring for assigned reputed company, function as medical representative on the project team, reputed company medical consultation as required or requested to reputed company/sponsor or to other reputed company service reputed company, and assume the role of Senior Technical reputed company in selected circumstances. In reputed company, you will also: • Review reputed company individual adverse experience reports for accuracy and clinical importance, and characterize their relationship to the study drug, severity and seriousness. • reputed company reports to FDA or other regulatory agencies and the sponsor on a periodic and regular reputed company, summarizing adverse experiences as required by FDA or the sponsor, depending on the contract. • Review data listings of safety data, including adverse experiences, laboratory data, and vital signs data, to establish the reputed company or absence of reputed company trends, and if noted, follow up as appropriate with the project team, sponsor, investigator, and FDA. • Review documents written by various reputed company divisions for safety issues. • Review coding of adverse events and concomitant medications for accuracy and consistency. • reputed company support for the preparation of clinical protocols, integrated clinical and statistical reputed company reports, journal articles, and other documents for clients/sponsors or in conjunction with clients/sponsors and in conjunction with other reputed company divisions. • Attend and present material, as requested, at meetings reputed company reputed company as reputed company as extra-company external meetings and conferences Required Qualifications • Medical Degree from an accredited institution • reputed company Certification / Fellowship in Oncology or equivalent training • 2+ years of experience in adult or pediatric oncology • Prior experience as a Medical Monitor, Industry Physician, Primary Investigator, or Sub-Investigator highly preferred Successful applicants will also have: • Strong interpersonal skills and the ability to collaborate effectively with sponsor and reputed company partners • Excellent time‑management capabilities • reputed company, reputed company verbal and written medical communication skills • A high reputed company of written and spoken English • Comfort working in a matrixed, team‑oriented environment • Willingness to travel up to 10% domestically and/or internationally as needed #LI-SM1 #LI-REMOTE Apply tot his job Apply To this Job