Medical Monitor- Pulmonologist EU
Medical Monitor- Pulmonologist EU
Posted on :
20-01-2025
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1 Vacancy
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Job Description
Job Title: Medical Monitor Pulmonologist EU
Job Location: London UK
Job Location Type: Remote
Job Contract Type: Fulltime
Job Seniority Level: MidSenior level
For the past 20 years ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech med device and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. As the world’s largest RCO (Research Consulting Organization) ProPharma partners with its clients through an advisebuilrate model across the complete product lifecycle. With deep domain expertise in regulatory sciences clinical research solutions quality & compliance pharmacovigilance medical information and R&D technology ProPharma offers an endtoend suite of fully customizable consulting solutions that derisk and accelerate our partners’ most highprofile drug and device programs.
ProPharma are looking for two pulmonologists or someone with extensive pulmonology experience to support our client on multiple studies across Europe (remote site monitoring only).
Physician 1
Starting 1st February 46 hours per week required per study. Study 1: COPD and study 2: Asthma
Physician 2
Starting ASAP 57 hours per week required. Study: pulmonary fibrosis
Essential Functions
***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please no phone calls or emails to anyone regarding this posting.***
ProPharma are looking for two pulmonologists or someone with extensive pulmonology experience to support our client on multiple studies across Europe (remote site monitoring only).
Physician 1
Starting 1st February 46 hours per week required per study. Study 1: COPD and study 2: Asthma
Physician 2
Starting ASAP 57 hours per week required. Study: pulmonary fibrosis
Essential Functions
- Directs the management of medical monitoring during clinical trials and projects and performs all aspects of clinical trial medical monitoring.
- Completes the medical review of key clinical documents individual case safety reports and medical or safetyrelated regulatory documents.
- Provides support and input into the planning design preparation initiation and execution of study protocols and other required documentation in compliance with project plans federal regulations GCP and good medical practice.
- Manages the evaluation and selection of investigators and study sites as well as analysis of medical activities.
- Reviews edits and oversees medical and safety sections of regulatory document submissions.
- Participates in Investigator’s meetings as needed.
- Other duties as assigned.
- Excellent understanding of the clinical / pharmaceutical process to effectively communicate and create required deliverables.
- Advanced knowledge of and ability to apply GCP and all applicable regulations and guidelines.
- Exceptional leadership skills and proven industry vision.
- Ability to understand complex clinical and statistical data and issues from an analytical standpoint.
- Effective negotiation and interpersonal communication skills to interact with a variety of peers and constituents.
- Track record of execution on large scale programs that meet quality time and budget requirements.
- A Doctor of Medicine (MD)
- A board certified Pulmonologist would be additional
***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please no phone calls or emails to anyone regarding this posting.***
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Employment Type
Full Time
Key Skills
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