This range is provided by Alimentiv. Your actual pay will be based on your skills and experience - talk with your recruiter to learn more. Base pay range In this role you will be providing unbiased medical guidance to clinical sites and internal and external study operations teams. You will also be providing therapeutic and compound training, medical guidance on protocol compliance, ensuring medical congruency at subject and study level and oversight of coding of medical terms. You will be responsible for supporting clinical safety, project, and data management by reviewing critical study materials at study start-up stage and data listings through the study duration. You may also assist with reviewing the interim or final data sets and the writing of the final study report. Day to day you will be in regular communication with the medical team (including medical teleconferences), and interfacing with the internal cross-functional teams as well as sponsor medical groups throughout the study. Medical Oversight

Provide clarity on general protocol questions and medical guidance for protocols as required
Serve as medical expert providing guidance on patient eligibility and investigational product related questions
Document contacts in accordance with Alimentiv or study-specific procedures
Consult with Alimentiv Medical Director(s), Sponsor Medical group and/or Safety about medical questions pertaining to the indication/compound under study
Observe and identify safety issues and other trends as appropriate
Provide consultation on the unbinding of trial participants/site staff to subject treatment allocation
Review individual out-of-range laboratory values following study-specific laboratory guidelines and alert values (as appropriate). Review cumulative laboratory values according to the study plans
Review protocol deviation data and recommend protocol changes as appropriate
Create and follow a study-specific medical monitoring plan if applicable
Provide medical review of study-level data to identify gaps and areas requiring additional safety-related follow-up
Participate in the development, review and finalization of protocols, amendments, Clinical Study Reports, as required
Provide medical input into data collection tools, study plans (e.g., monitoring, statistical analysis plans, etc.)
Provide medical input into study feasibility, site selection and site initiations as required
Attend and lead medical monitoring teleconferences at regularly scheduled intervals throughout the study, if required
Maintain a thorough working knowledge of protocol(s) and the current Investigator Brochure(s) with particular attention to safety data involving human subjects
Participate in the development and maintenance of medical educational materials
Provide internal training to Alimentiv operational teams on specific diseases, drug targets, pharmacology, protocol requirements, etc., as needed to support execution of client studies or general acquisition to appropriate medical knowledge as required by the organization
Assist with the development of investigator training and meeting support materials
Attend and present at investigator meetings and CRA training meetings
The successful candidate must have a medical degree with a strong understanding of the drug development process, ICH and Good Clinical Practices. Typically, this person will hold about 4-6 years of related experience with substantial ongoing job-related training
Strong written and verbal communication and presentation skills, enabling effective interactions with team members within Alimentiv, client company personnel and prospective sponsors
Ability to exercise sound clinical judgment in addressing protocol ambiguities and unforeseen medical scenarios that arise during trial conduct. Strong analytical and critical thinking skills are essential for identifying safety signals, evaluating complex patient data, and recognizing emerging trends across study populations to ensure subject protection and data integrity
Previous experience in clinical trials preferred, especially in navigating complex medical scenarios within a CRO environment
Must be fluent in English
Seniority level: Not Applicable
Employment type: Full-time
Job function: Other
Industries: Pharmaceutical Manufacturing
Location: Edinburgh, Scotland, United Kingdom

The successful candidate must have a medical degree with a strong understanding of the drug development process, ICH and Good Clinical Practices. Typically, this person will hold about 4-6 years of related experience with substantial ongoing job-related training
Strong written and verbal communication and presentation skills, enabling effective interactions with team members within Alimentiv, client company personnel and prospective sponsors
Ability to exercise sound clinical judgment in addressing protocol ambiguities and unforeseen medical scenarios that arise during trial conduct. Strong analytical and critical thinking skills are essential for identifying safety signals, evaluating complex patient data, and recognizing emerging trends across study populations to ensure subject protection and data integrity
Previous experience in clinical trials preferred, especially in navigating complex medical scenarios within a CRO environment
Must be fluent in English

Medical Monitor