Job Title

#hiring - Remote OpportunityVeeda Lifesciences looking for "Clinical Research Physician" About the Role:The Clinical Trial Physician is responsible for providing medical input within the organization as well as to external partners and performing medical review tasks within the context of clinical trials. Furthermore, the Clinical Trial Physician is responsible for undertaking scientific/medical writing tasks within the organization.Responsibilities:All study related documents that fall under the Clinical Science Department scope (e.g., Study Protocols, ICFs - in collaboration with other departments e.g., Clinical Operations, Regulatory, as required -, Pharmacy Manuals, Medical Review Plans, etc.)Scientific presentations and manuscriptsMedical training material (i.e. therapeutic area and study protocol training material)Delivers internal and external study protocol and therapeutic area training coursesProvides medical expertise and consultation within the Company on key therapeutic areas of the clinical development programProvides guidance to all involved departments on the medical and scientific aspects of the assigned clinical trials/projectsResponds to medical queries from all involved parties in assigned clinical trials (e.g., CRAs, Project Managers, Clinical Operations Managers, Investigators) and collaborates with all concerned staff in maintaining an up-to-date study-specific Q&A logIs available 24/7 to respond to urgent medical/protocol related issues derived from an Investigational Site, as applicablePerforms periodic medical review of the data from clinical trials according to the study-specific Medical Review Plan requirements (e.g., review of eligibility, review of efficacy and safety data)Performs real-time medical review on urgent medical and safety issues, as neededCollaborates with and provides medical input to the Data Management staff to ensure the successful development of the study-specific eCRFAttends Investigator Meetings and Conferences, as applicableComplies with the Company's Quality and Information Security Management Systems and applicable national and international legislation, including legislation for data protection and ICH GCP requirements Qualifications:MD (After MBBS)Experience Required:4 - 8 YearsWorking Hours:European working hoursPay range and compensation package:Up to 30 LPA