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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, comprehensive training, and opportunities for professional growth.
- Other info: Full-time role based in Edinburgh with excellent career advancement opportunities.
- 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.
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 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
Medical Monitor employer: Alimentiv
Contact Detail:
Alimentiv Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Medical Monitor
✨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 with a friend or using mock interview platforms to boost your confidence.
✨Tip Number 3
Showcase your expertise! During interviews, be ready to discuss specific scenarios where you exercised sound clinical judgment. This will demonstrate your ability to handle complex medical situations effectively.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take the initiative to engage directly with us.
We think you need these skills to ace Medical Monitor
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experience mentioned in the job description. Highlight your medical degree, clinical trial experience, and any relevant training you've done. We want to see how you fit into our team!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about the role of Medical Monitor and how your background aligns with our needs. Keep it engaging and personal – we love a good story!
Showcase Your Communication Skills: Since this role involves regular communication with various teams, make sure to demonstrate your strong written and verbal communication skills in your application. We want to know how you can effectively interact with both internal teams and external sponsors.
Apply Through Our Website: We encourage you to apply directly through our website for the best chance of getting noticed. It’s super easy, and you’ll be able to keep track of your application status. Plus, we love seeing applications come through our own channels!
How to prepare for a job interview at Alimentiv
✨Know Your Protocols
Before the interview, make sure you have a solid understanding of the protocols and guidelines relevant to the role. Familiarise yourself with ICH and Good Clinical Practices, as well as any specific studies Alimentiv is currently involved in. This will show your commitment and expertise.
✨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 Scenarios
Anticipate questions related to clinical safety and protocol compliance. Think about potential challenges you might face in the role and how you would address them. Being able to discuss these scenarios confidently will highlight your analytical and critical thinking skills.
✨Engage with Questions
At the end of the interview, don’t forget to ask insightful questions. Inquire about the team dynamics, ongoing projects, or how success is measured in the role. This shows your genuine interest in the position and helps you assess if it's the right fit for you.