Associate Medical Director / Oncologist (Brazil)

At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.We are looking for an Associate Medical Director to join our A-team (remote). As an Associate Medical Director at Allucent, you are responsible for working independently to ensure the medical/clinical and safety integrity and quality of trials conducted by Allucent, serving as the medical monitor contact in study protocols to investigators and study sites team regarding protocol related questions and safety of the subjects enrolled. Experience in Oncology is a requirement for this position.In this role your key tasks will include:Independently provide medical monitor support to assigned clinical studies, for example answering medical questions from study team and/or site, assist with protocol interpretation and medical review of generated data including but not limited to clinical laboratory data and case report forms as necessary to ensure adherence to the protocol, consistency and scientific validity of the data. When appropriate, and with the necessary support from senior colleagues, assist the Project Manager in discussions with clients on safety issues or concerns that may have arisenPrepare the Medical Monitoring and other relevant plans for assigned studies conducted by Allucent prior to the start of the study and in accordance to deliverables contracted.Review Serious Adverse Events, SUSARs, safety narratives and perform Analysis of Similar EventsAssist clinical data management with MedDRA and WHO coding in assigned trialsAssist by reviewing clinical study documents for medical consistency and relevance, with support of senior medical team members if needed, including but not limited to the clinical trial protocol (CTP), the Informed Consent (ICF) and clinical study report (CSR) other safety reports (e.g., DSUR, PSUR)Assist in the set up and conduct of Data Safety Boards (DSMB, DMB or similar) and Dose escalation meetings (DEC)Attend, participate and present in Kick-Off, Investigators' meeting, and other relevant meetings in assigned projects, as requested.Provide 24/7 urgent medical support for medical and safety advice if requiredTraining of project teams on medical aspects of the trial and therapeutic training as requiredReview of Protocol DeviationsIdentify study risks and provide input to the Risk planReview and understand study medical deliverables laid down in the assigned study's contract with support of senior colleagues and help track budget spent throughout their assigned study(ies)Attends and may need to present at major therapeutic conferences and drug development conferencesAssure good communication and relationships with (future) clientsContribute and take part with support from senior colleagues as needed in client evaluations, visits and bid defensesRequirementsTo be successful you will possess:MD degreeExperience as OncologistMinimum 3 years of relevant work experience with solid Oncology expertiseGood knowledge of GxPGood standing with local, state (in the US), and national licensing and regulatory authorities and certifying bodiesGDPR/HIPAA, CFR/CTR/CTD and applicable (local) regulatory requirements understandingStrong written and verbal communication skills including good command of English language Representative, outgoing and client focused Ability to work in a fast-paced challenging environment of a growing companyAdministrative excellence Proficiency with various computer applications such as Word, Excel, and PowerPoint requiredBenefitsBenefits of working at Allucent include:Comprehensive benefits package per locationCompetitive salaries per locationDepartmental Study/Training Budget for furthering professional developmentFlexible Working hours (within reason)Opportunity for remote/hybrid* working depending on locationLeadership and mentoring opportunitiesParticipation in our Buddy Program as a new or existing employeeInternal growth opportunities and career progressionFinancially rewarding internal employee referral programAccess to online soft-skills and technical training via ADP and internal platformsEligibility for our Spot Bonus Award Program in recognition of going above and beyond on projectsEligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employeesDisclaimers:*Our hybrid work policy encourages a dynamic work environment, prescribing 2 days in office per week for employees within reasonable distance from one of our global offices. "The Allucent Talent Acquisition team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively "Allucent"). Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third-party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources."