Senior Project Manager

Planet Pharma; Germay; Sur place; EUR 95 000 - 155 000; Plein temps

Résumé du poste

Planet Pharma is seeking a Senior Clinical Project Manager for Dermatology & Immunology studies. You will drive Phase II-III trials from start-up through close-out, coordinating sponsors, timelines, budgets, vendors, and cross-functional teams to ensure quality and regulatory compliance.

Ideal candidates have 7+ years in clinical research and 5+ years in Clinical Project Management, with recent Rheumatology, Dermatology, or Immunology experience and strong ICH-GCP knowledge.

Qualifications

• Bachelor's degree in a Life Sciences discipline.
• 7+ years of clinical research experience.
• Minimum 5 years of Clinical Project Management experience.
• Recent Rheumatology, Dermatology and/or Immunology experience is ideal.
• Experience leading global, multi-center Phase II-III clinical trials.
• Experience managing trial budgets exceeding $3M USD.
• Strong knowledge of ICH-GCP, FDA, and international clinical regulations.
• Fluent English (written and verbal).

Responsabilités

• Act as the primary sponsor contact and lead client communications
• Manage study timelines, budgets, resources, vendors, and deliverables
• Lead global cross-functional project teams
• Oversee protocol implementation, study plans, investigator meetings, and study execution
• Monitor project risks, quality metrics, and audit readiness
• Manage recruitment performance and mitigation strategies
• Coordinate activities across Clinical Operations, Data Management, Biostatistics, Regulatory Affairs, and Scientific teams
• Identify and manage change orders and out-of-scope activities

Connaissances

Leadership

Stakeholder management

Communication skills

Fluent English

Formation

Bachelor's degree in Life Sciences

Description du poste

Senior Clinical Project Manager – Dermatology & Immunology Studies

Summary

As a Senior Clinical Project Manager, you will lead the delivery of Phase II-III clinical trials, serving as the primary point of contact for sponsors while overseeing timelines, budgets, vendors, and cross-functional teams. You will drive study execution from start-up through close-out, ensuring high-quality delivery and regulatory compliance across global programs.

Responsibilities

• Act as the primary sponsor contact and lead client communications
• Manage study timelines, budgets, resources, vendors, and deliverables
• Lead global cross-functional project teams
• Oversee protocol implementation, study plans, investigator meetings, and study execution
• Monitor project risks, quality metrics, and audit readiness
• Manage recruitment performance and mitigation strategies
• Coordinate activities across Clinical Operations, Data Management, Biostatistics, Regulatory Affairs, and Scientific teams
• Identify and manage change orders and out-of-scope activities

Requirements

• Bachelor's degree in a Life Sciences discipline
• 7+ years of clinical research experience
• Minimum 5 years of Clinical Project Management experience
• Recent Rheumatology, Dermatology and/or Immunology experience is ideal
• Experience leading global, multi-center Phase II-III clinical trials
• Experience managing trial budgets exceeding $3M USD
• Strong knowledge of ICH-GCP, FDA, and international clinical regulations
• Excellent leadership, stakeholder management, and communication skills
• Fluent English (written and verbal)

Planet Pharma is an American parented Employment Business/Agency that provides global staffing services with its headquarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.

Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognized by FORBES as the 17th best professional staffing firm and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing.

We are an equal opportunities Recruitment Business and Agency. We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.

www.planet-pharma.com