Ref #: 28547

Employment type: Permanent - Full-Time

Location: Seoul, South Korea

Posted: 20-Apr-2021

Description

If you are seeking a career where you can truly make a difference in the lives of others, working closely together with the top minds in the pharmaceutical Industry, then here is your chance. We are hiring a Clinical Research Associate to work closely with our client, a leading pharmaceutical company.

Overview
Site engagement is a critical component in the execution of a clinical trial. Engagement of highly motivated clinical investigators will enable company to maximize efficient and timely delivery of clinical trials. This position is responsible for contributing to an industry leading site engagement team. The Site Engagement Manager is responsible for providing operational expertise to sites through ownership/management of Site Engagement Strategy.

Key responsibilities
The responsibilities of the Site Engagement Manager may include, but are not limited to:
• Develop, communicate, and execute Site Engagement Strategy/Plan working closely with the Clinical Team and key internal stake holders throughout the life cycle of clinical trials
• Support the clinical team in coordinating and executing site engagement activities by understanding the competitive landscape, capturing trial hurdles and using motivational tactics to ensure timely delivery of trials
• Engage, evaluate and develop a global network of high performing sites through coordinated, consistent interactions using multiple communication channels to create awareness of and its activities thereby increasing their desire to partner
• Develop & maintain relationships with site engagement organizations; assist in identification of high performing sites and key opinion leaders that can contribute to forums, boards and/or discussions
stakeholders/customers
• Support assigned studies from a regional and cultural perspective & support study teams with quality related visits as needed
• Work with strategic partners to ensure alignment on systems and processes for identifying and engaging sites

Required experience and qualifications
• A minimum of 5 years of experience in the Pharmaceutical, Biotechnology, and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e.g. clinical project manager, study director/coordinator, clinical research associate, patient/site engagement companies)
• Proven track record of success on cross-functional projects in a global environment.
• Good working knowledge of GCP guidelines in different regions

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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