Ref #: 28196

Employment type: Permanent - Full-Time

Location: Poland

Posted: 03-Apr-2021

Description

We are looking to recruit a Lead CRA/ Principal CRA who would be interested in taking a step up in his/her career as a Clinical Trial Manager and work closely with our client, a leading pharmaceutical company.

Overview:
The Clinical Trial Manager will be responsible for project-managing the Clinical Operations teams such as CRAs, CTAs and additional project staff, to ensure delivery of country and site level study activities in alignment with the global study project plan.

Key Responsibilities:
• Leading the regional matrix team (e.g. CRA, CTA, etc.) to ensure delivery of country and site level study activities in alignment with the global study project plan
• Identifying and resolving issues at a regional level (CEE)
• Collaborating with Global CTM to ensure country level study delivery is aligned with the global study project plan
• Contributing to study-level risk assessments
• Leading and continually review regional risk mitigation activities to ensure study delivery to plan
• Overseeing regional insourcing/outsourcing partner deliverables to the required standards
• Partnering with Tech Services, Supplier Governance and Electronic Trial Operations - to ensure regional, country and site vendor set-up, conduct and quality Leading regional documentation and required tool and systems set-up
• Contributing to regional aspects of Drug Supply Plan
• Ensuring implementation of study(ies) in accordance with SOPs and ICH/GCP guidelines
• Review of monitoring visit reports

Required experience and qualifications:
• BA/BS/BSc in the sciences or previous experience in a similar role
• Strong on-site monitoring experience (CRA) is required - ideally a minimum of 4 years
• Previous clinical study management experience (either local or in a region) would be an advantage (Principal/Lead CRA, CTM, LTM)
• Experience in oversight of clinical research vendors (CROs, central labs, imaging vendors, etc.)

How to apply?
This is an exceptional opportunity within a global organisation who offers rewarding careers. If you want to be a part of this exciting opportunity who offers a competitive salary, excellent benefits package, please contact Dariusz Sternlicht, Recruitment Consultant at DOCS and email your up-to-date CV to: dariusz.sternlicht@docsglobal.com

Why join the DOCS team at ICON?
Working at ICON is more than a job, it’s a calling for people who care and are passionate about improving patients’ lives. At ICON, we care about our people and your passion, you are key to our success. We aim to provide an open and friendly work environment where we empower our people and provide them with opportunities to develop their long-term career.

It takes courage to move from one job to another, the process involves careful consideration. Reach out having the conversation that would change your life and the lives of our patients. Our team of recruitment experts will provide the information you need in making the right decision.

At ICON you will have the opportunity to work with one of the global top 20 pharmaceutical companies, working on novel therapies that deliver real impact. If you want a career with a difference, ICON is the place for you.

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