Medical Monitor- Pulmonologist, EU

Job title:

Medical Monitor- Pulmonologist, EU

Company

Lifelancer

Job description

Job Title: Medical Monitor- Pulmonologist, EUJob Location: London, UKJob Location Type: RemoteJob Contract Type: Full-timeJob Seniority Level: Mid-Senior levelFor 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 advise-build-operate 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 end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners’ most high-profile 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 1Starting 1st February, 4-6 hours per week required per study. Study 1: COPD and study 2: AsthmaPhysician 2Starting ASAP, 5-7 hours per week required. Study: pulmonary fibrosisEssential 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 safety-related 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.

Necessary Skills And Abilities

• 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.

Educational Requirements

• A Doctor of Medicine (MD)
• A board certified Pulmonologist would be additional

We celebrate our differences and strive to create a workplace where each person can be their authentic self. We are committed to diversity, equity, and inclusion. Employees are encouraged to unleash their innovative, collaborative, and entrepreneurial spirits. With a holistic approach as an Equal Opportunity Employer, we provide a safe space where all employees feel empowered to succeed.***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***Lifelancer ( ) is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains.For more details and to find similar roles, please check out the below Lifelancer link.

Expected salary

Location

London

Job date

Sun, 19 Jan 2025 23:45:45 GMT

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