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1 VAGA DE Médico EM Goiânia / GO
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Medical director/senior medical director - Hem/onc remote latin america as a leading global contract research organization (cro) with apassion for scientific rigor and decades of clinical developmentexperience, fortrea provides pharmaceutical, biotechnology, andmedical device customers a wide range of clinical development, patientaccess and technology solutions across more than 20 therapeutic over 19,000 staff conducting operations in more than 90countries, fortrea is transforming drug and device development forpartners and patients across the globe. Did you know? Labcorpsclinical development and commercialization services business is nowfortrea in connection with its planned spin-Off from labcorp, which isexpected in mid-2023. Fortreas spin-Off from labcorp is subject tosatisfaction of certain customary conditions. This spin-Off willposition both organizations for accelerated growth and allow each tofocus resources on distinct strategic priorities, customer andemployee needs and value creation a provider of phasei-Iv clinical trial management, regulatory guidance, patient accesssolutions and market access consulting, fortrea will partner with bothemerging and large pharmaceutical, biotechnology, device anddiagnostic companies to drive healthcare innovation and improve thelives of patients worldwide. Fortrea is looking for problem-Solversand creative thinkers who are passionate about breaking down barriersfaced by sponsors of clinical trials, and who are committed to helpingtransform the development process to get promising life-Changing ideasand therapies to patients faster. Join us as we cultivate a workspacewhere all employees have the opportunity to grow and make impacts on aglobal scale. For more information and questions related to fortrea,please visit . Discover new opportunities to grow your career as asenior medical director / medical director at labcorp drug developmentthe primary role of this senior medical director / medical directorposition is to provide subject matter expertise and medical monitoringin support of advancing clinical trials and drug development partnership with labcorp drug development clients, he/she will beexpected to be a key contributor to the medical strategy and executionof clinical programs. Furthermore, the medical director willparticipate in client relations and business development activitiesrepresenting labcorp drug development in proposals and industrymeetings as needed. This is a remote home-Based role based in thelatin americal with travel (global) as needed. What to expect clientrelationship & business development activities: develop new andenhance existing client relationships where possible providesleadership and presents medical/scientific capabilities to clients asa participant of a proposal team leverage known and builds newrelationships with investigators/sites to performs site/ investigatorfeasibility and to support optimal recruiting and conduct of trialsable to present or serve on panels to represent the company atconferences and scientific meetings. Therapeutic and scientificexpertise responsible for medical and safety monitoring on assignedprojects - Develops training modules and materials, and providestraining in disease states and protocol specific requirementsparticipates in training opportunities to advance knowledge of drugdevelopment and good clinical practice guidelines serve as global leadproject physician and provides clinical and medical expertise mayserveas a program level physician across multiplestudiesfor a given companyprovides subject matter and drug development expertise to be a keycontributor to the medical strategy and execution of the program forthe client performs medical data review and/or oversight of centralmedical data review- Laboratory values, adverse events, codingdictionaries and data tables, listings and figures as needed, holisticand aggregated data review develops, reviews and revises protocols,case report forms, training materials, project specific tools,analysis plans design, clinical trial reports and new drugapplications - Prepares materials for investigator meetings activelyparticipates in investigator meetings provides medical/scientificexpertise to project teams and to other labcorp drug developmentdepartments interacts with inter-Departmental and external consultantsas appropriate - Participates in feasibility discussions relating tospecific project proposals - Participates in project risk assessmentactivities assists when needed with data safety monitoring boardactivities contributes to the scientific strategic leadership for theprograms education / experience: md degree with fellowship training inhematology / oncology board certification preferred. Excellentcommunication and interpersonal skills - Ability to travelqualifications: 3 years of clinical research experience with a cro,pharmaceutical company, research experience in academics preferred -Strong knowledge and experience with clinical trials previousexperience in medical practice/patient care prior clinical /laboratory research experience in a fellowship / academic setting alsopreferred labcorp is proud to be an equal opportunity employer: as aneoe/aa employer, labcorp strives for diversity and inclusion in theworkforce and does not tolerate harassment or discrimination of anykind. We make employment decisions based on the needs of our businessand the qualifications of the individual and do not discriminate basedupon race, religion, color, national origin, gender (includingpregnancy or other medical conditions/needs), family or parentalstatus, marital, civil union or domestic partnership status, sexualorientation, gender identity, gender expression, personal appearance,age, veteran status, disability, genetic information, or any otherlegally protected characteristic. We encourage all to apply. For moreinformation about how we collect and store your personal data, pleasesee our privacy statement .
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