Clinical Project Manager - Oncology in London

Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas: Oncology, Rare Disease and Neuroscience. Supported by nearly 100 years of development experience, with global hubs in the U.K, we tackle areas of high unmet medical need through research and innovation. Our passionate teams in more than 40 countries are focused on what matters and endeavour every day to bring medicines to patients in 88 countries.

Job Description:

• Lead, manage and drive the cross-functional Clinical Study Team and Contract Research Organization (CRO) in collaboration with the CDPDs and Ipsen team members responsible for the study.
• Oversee and drive cross-functional leadership and expertise to ensure effective contribution, execution, and delivery of study activities as per quality, plan/timelines, and budget.
• Foster a team approach to all activities associated with the implementation, conduct and closing of clinical studies including Ipsen clinical study team members.
• Establish and maintain excellent professional relationships with Services Providers and the clinical study team through regular communication.
• Lead clinical project processes, managing all operational aspects for implementation and conduct of global clinical trial activities from study start-up to CSR, in respect of GCPs and relevant SOPs.
• Develop, manage, and execute assigned projects, including setting up study teams and leading regular internal Study Team meetings.
• Provide expertise to clinical outsourcing specifications and purchasing to facilitate RFP documents and selection of Services Providers.
• Accountable for the development, management and tracking of trial budget working closely with finances and service provider representatives.
• Ensure appropriate oversight of Services Providers and other external vendors activities.
• Supervise country feasibility and site selection processes to identify and gain approval for high quality investigators and study sites.
• Provide support and oversee the activities of the Clinical Trial Associate (CTA) assigned to the study.
• Work with the SP, Patient Affairs office, and digital team to develop and approve a recruitment strategy and communication tools.
• Participate in meetings led by SP and ensure timely and accurate completion of project milestones.
• Travel as needed to observe and discuss projects, build positive working relationships, and maintain enthusiasm regarding projects.
• Coordinate post quality audit hosted by Sponsor and ensure CAPA implementation by SP.
• Assist Quality Assurance within inspections preparation as applicable.
• Participate in the preparation and review of clinical study reports.
• Liaise with relevant Ipsen or Service Providers teams to ensure the posting of the clinical study and results on required registries.

Education / Certifications:

• Bachelor’s degree in life science or medical graduate preferred, or relevant qualifications.

Experience:

• Minimum of 3 years working in clinical research with management of clinical activities for the set up and running of international registrational studies.
• Experience in managing and developing relationships with Contract Research Organizations (CROs/SPs).
• Fluent English.
• Ability to work in a strongly regulated environment within a quality management system (QMS).
• Advanced knowledge of software applications (e.g., Word, Excel, PowerPoint, Adobe Reader).
• Basic Financial Knowledge.
• Good understanding of the drug development process and knowledge of the pharmaceutical industry environment.
• Excellent leadership skills and capability to work within a team.
• Strong verbal and written communication skills (English).

Compensation:

The annual base salary range for this position is $144,000 - $200,000. Individual compensation within this range depends on various factors, including prior education and experience, job-related knowledge and demonstrated skills.

This job is eligible to participate in our incentive compensation program as well as our long-term incentives program. At Ipsen, we offer a comprehensive employee benefits package, including 401(k) with company contributions, group medical, dental and vision coverage, life and disability insurance, short- and long-term disability insurance, parental leave, paid time off, and much more.

The value we place on different perspectives and experiences drives our commitment to inclusion and equal opportunities.

Location: London (UK)

Type: Full time