Are you a Physician with a strong clinical research background in Infectious Diseases / Vaccines?
We are recruiting for a North and Latin Americas based Associate Medical Director, specializing in Infectious Diseases / ICU experience.
This is an exciting opportunity to work on cutting edge COVID 19 and other ID Projects.
As a key position within the organization with a level of visibility and leadership, this is an ideal role for someone looking to step into a Medical Director or above-country leadership role.
You will be responsible for : Answering day to day medical and scientific questions, provide daily medical support to our staff or site (investigator / study coordinator)Review and sign off Data Management listings of safety data(including adverse events, laboratory data, vital signs data, medical history, physical examination, concomitant medication), establish the presence or absence of clinically meaningful trends and, if noted, follow up as appropriate with the project team, sponsor, investigator, and Regulatory AuthoritiesReview and sign off technical documents written by Parexel with respect to medically relevant matters with particular attention to those relating to drug safetyReview coding of adverse events and concomitant medications for accuracy and consistencyProvide support for the preparation of clinical protocols, integrated clinical and statistical summary reports, journal articles, and other documents for clients / sponsors in conjunction with clients / sponsors or in conjunction with other Parexel departmentsAttend and present material (such as therapeutic area training) as requested, at internal and external meetings (e.
g. investigator meetings)Provide input as necessary to Feasibility Studies, Data Monitoring Committees (DMCs), Clinical Endpoint Committees (CECs).
however, Board Certified Internal Medicine Physicians and Pediatricians with extensive Infectious Disease experience will also be consideredMPH or PhD is advantageousClinical specialization in Infectious Diseases / Internal medicineExperience in clinical trials is preferredInvestigator experience in clinical trials is preferredDemonstrated competence as a Study Director / Medical Monitor / Research Physician / Clinician Scientist / Principal Investigator / Sub-Investigator / Clinical Scientist / Clinical Researcher / Medical Advisor / Study Physician / Clinical Development Physician and prior experience working with the FDA or EMEA on responses to inquiries for study related information is not required, but is a plusPrevious CRO experience is preferred, but other strong candidates will be consideredThe ability to travel up to 20% will be required in the future
For immediate consideration, please submit resumes in English for review
2021-05-19 00 : 05 : 32