Ref #: 29246

Employment type: Permanent - Full-Time

Location: Ukraine

Posted: 18-May-2021

Description

Overview:
In this role you will act as a primary point of contact to lead, manage and co-ordinate the conduct of clinical trials from study start-up to close out at a country (local) level. You will maintain the quality and scientific integrity of clinical trials at a country level

Key Responsibilities:
• Planning, management and oversight of clinical study execution in accordance with the global program strategy, through leadership of the cross-functional Local Study Team (LST)
• Accountable for study deliverables in that country.
• Leads country-level operational planning and supports site selection within region
• Contribute to development of study-specific materials – e.g. monitoring plan, study specific training documents.
• Provides input into the Country Operational Plan (COP) and partner with the DFM and GCTM to ensure regional delivery of the Global Study Operational Plan (GSOP)
• Support and contribute to Trial Management Teams (TMTs), agenda driven presence at meetings and daily huddle as required
• Communicate country status (including timelines and deliverables) to key stakeholders (e.g. TMT, GCTM, Program Managers) and ensures updates to relevant systems
• Contributes to site-level goal setting and study-specific deliverables for clinical sites within their country
• Oversight and monitoring of applicable vendor activities eg. laboratories and equipment provisioning
• Contribute to the study-level forecast for investigational product, support study level accountability and reconciliation across multiple countries, management of ELE process
• Member of the Global Clinical Studies Team (GCST)

Required experience and qualifications:
• BA/BS/BSc in the sciences or previous experience in a similar role
• Previous clinical study management experience on a country level
7 years work experience in life sciences or medically related field, including 4 years of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company
• 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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