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- Tasks: Provide medical guidance and oversight for clinical trials, ensuring safety and protocol compliance.
- Company: Join Alimentiv, a leader in pharmaceutical manufacturing with a focus on innovation.
- Benefits: Competitive salary, professional development, and a supportive team environment.
- Why this job: Make a real impact in drug development while working with a dynamic medical team.
- Qualifications: Medical degree and experience in clinical trials required; strong communication skills essential.
- Other info: Opportunity for career growth in a fast-paced, collaborative setting.
The predicted salary is between 36000 - 60000 £ per year.
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 those aspects relating to safety data involving human subjects.
Training- Participates 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. You must have the 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 is preferred especially in navigating complex medical scenarios within a CRO environment. Must be fluent in English.
Medical Monitor in Cambridge employer: Alimentiv
Contact Detail:
Alimentiv Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Medical Monitor in Cambridge
✨Tip Number 1
Network like a pro! Reach out to your connections in the medical field, especially those who work at Alimentiv or similar companies. A friendly chat can lead to insider info about job openings and even referrals.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of clinical trials and safety protocols. We recommend practising common interview questions related to medical monitoring and being ready to discuss your past experiences in detail.
✨Tip Number 3
Showcase your communication skills! During interviews, make sure to highlight how you’ve effectively communicated complex medical information to diverse teams. This is key for roles like Medical Monitor where collaboration is crucial.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re genuinely interested in joining the team at Alimentiv.
We think you need these skills to ace Medical Monitor in Cambridge
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter for the Medical Monitor role. Highlight your relevant experience in clinical trials and any specific skills that match the job description. We want to see how you fit into our team!
Show Off Your Communication Skills: Since this role involves a lot of communication with various teams, emphasise your written and verbal communication skills. Share examples of how you've effectively communicated complex medical information in the past. We love clear communicators!
Be Detail-Oriented: Attention to detail is key in this role. When filling out your application, double-check for any errors or inconsistencies. We appreciate candidates who take the time to ensure their application is polished and professional.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy – just follow the prompts!
How to prepare for a job interview at Alimentiv
✨Know Your Protocols
Make sure you have a solid understanding of the protocols and guidelines relevant to the role. Brush up on ICH and Good Clinical Practices, as well as any specific studies that Alimentiv is currently involved in. This will show your commitment and expertise during the interview.
✨Showcase Your Communication Skills
As a Medical Monitor, you'll need to communicate effectively with various teams. Prepare examples of how you've successfully navigated complex medical scenarios or communicated critical information in past roles. This will demonstrate your ability to interact with both internal teams and external sponsors.
✨Prepare for Clinical Safety Questions
Expect questions related to clinical safety and how you would handle protocol deviations or safety signals. Think through potential scenarios and be ready to discuss your analytical approach to identifying trends and ensuring subject protection.
✨Engage with the Interviewers
Don't just answer questions—engage with your interviewers. Ask insightful questions about their current projects, team dynamics, and how they approach medical oversight. This shows your genuine interest in the role and helps you assess if it's the right fit for you.