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Allucent is a full-service contract research and development organization with international resources dedicated to helping pharmaceutical and biotechnology companies efficiently and expeditiously navigate the regulatory approval process in order to bring new drugs, biologics, and medical devices to the people who need them. Allucent is a non-laboratory environment. At Allucent, our mission is to help bring new therapies to light. When you work at Allucent, that means rolling up your sleeves and applying your scientific knowledge, clinical expertise, and experience to partnerships with our clients in small and mid-sized biotech companies.These customers have new therapeutic ideas but want a partner who can assist with the clinical trial process, the complexities of certain disease states, or other critical capacities. You’ll work with them on the newest treatment breakthroughs for some of the most perplexing conditions. And ultimately, you’ll help make a positive difference in patients’ lives.We are looking for a Medical Director (Oncology) to join us in Europe! The Medical Director works independently to ensure the medical/clinical and safety integrity and quality of trials conducted by Allucent. Serves as the medical monitor contact in trial protocols to investigators and trial sites regarding protocol related questions and safety of the subjects enrolled. Advises investigators, project teams, and clients on safety issues arising from medicinal products, devices and trial designs undertaken by Allucent. Works along with more senior colleagues and internal team members, senior management and business development on issues and questions of any medical /clinical nature. Reviews SAEs, SUSARs and AEs reports and writes safety narratives in accordance with all applicable competent authority regulations and reporting standards. Reviews, if needed with support from more senior colleagues, protocols, investigator’s brochures, clinical trial reports written by Allucent ensuring they are approved in accordance with Allucent procedures and good medical practices. Supports Business Development efforts with support of senior colleagues by reviewing the proposal and attending client meetings including Bid Pursuit Meetings. Location: Europe Workplace: Hybrid/RemoteExperience: (all levels) Associate Medical Director / Senior Medical DirectorQualifications: MD DegreeTherapeutic Expertise: OncologyThe Medical Director (Oncology) is responsible for the following tasks:Medical Affairs Management Independently provide medical monitor support to assigned clinical trials, for example answering medical questions from trial 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 arisen Provide input on: Protocol design Strategic clinical recommendations Prepare the Medical Monitoring and other relevant plans for assigned trials conducted by Allucent prior to the start of the trial and in accordance to deliverables contracted. Review Serious Adverse Events, SUSARs, safety narratives and perform Analysis of Similar Events Assist clinical data management with MedDRA and WHO coding in assigned trials Assist by reviewing clinical trial 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 trial 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 required Training of project teams on medical aspects of the trial and therapeutic training as required Support protocol deviation guidance development and review of Protocol Deviations Identify trial risks and provide input to the Risk plan Ensure conduct of safety reviews to identify data issues, to evaluate data for safety and efficacy and to interpret trends including support to signal detection and evaluation strategies and risk minimization measures with support from senior colleagues Independently review and understand trial medical deliverables laid down in the assigned trial’s contract and track budget spent throughout their assigned trial(s) Draft and contribute with the support of senior colleagues as Subject Matter Expert (SME) in the field of Medical Monitor activities to the evaluation/improvement of processes and procedures within the Quality Management System Assure good communication and relationships with (future) clients Support Business Development efforts with support of senior colleagues by reviewing the proposal and attending client meetings including Bid Pursuit Meetings May advise and assist clients on product development, trial designs, endpoint analyses and the feasibility of conducting Phase I to IV clinical trials in countries proposed by Allucent. Liaise with country managers and department heads at Allucent as needed to meet this task May provide therapeutic consultation in support of the scientific, medical, and regulatory operations of the company, including medical assessments on a consultative basis for post marketing activities (e.g., product labelling, health hazard evaluations, etc.) Management, Learning & Development Active and independent support to staff learning & development within the company Attends and presents at major therapeutic conferences and drug development conferences and contributes to the scientific footprint of Allucent with webinars/white paper/blog posts in areas of their expertise Mentorship and line management role (optional) to the other medical staff within the department Keep up to date with developments in medical science Quality Management Review, improve medical affairs processes and procedures within the Quality Management System Understand medical affairs department processes and procedures within the Quality Management System and ensure his/her adherence to the procedures Account Management, Sales & Acquisition Assure strong long-lasting relationships with (future) key accounts Support in preparation of new proposals Contribute and take part in client evaluations, visits and bid defenses RequirementsQualifications MD degree Minimum 5 years of relevant work experience Very good knowledge of GxP Good standing with local, state (in the US), and national licensing and regulatory authorities and certifying bodies GDPR/HIPAA, CFR/CTR/CTD and applicable (local) regulatory requirements understanding Skills Strong 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 company Administrative excellence Proficiency with various computer applications such as Word, Excel, and PowerPoint required Benefits Comprehensive benefits package Competitive salaries per location Departmental Study/Training Budget for furthering professional development Flexible Working hours (within reason) Opportunity for fully remote/hybrid working Leadership and mentoring opportunities Internal growth opportunities and career progression More task variety Financially rewarding internal employee referral program Access to online soft-skills and technical training via GoodHabitz and internal platforms To all recruitment agencies: Allucent does not accept agency resumes. Please do not forward resumes to our careers alias or other Allucent employees. Allucent is not responsible for any fees related to unsolicited resumes.#LI-TCW
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