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Real-World Evidence Analyst I

Seoul, Seoul, Korea, Republic of

Job Description

Cerner Enviza is a leading global healthcare consulting firm and trusted advisor to many of the world’s top pharmaceutical, biotech, and medical device & diagnostic companies. By supporting the work of Cerner Enviza, you will work with world-class healthcare companies, helping them improve global access to medicines by connecting science and research. Cerner Enviza is passionate about our people, our business, and our clients and is proud to foster a culture that contributes to the health and well-being of humankind. Leading through innovation, we consistently challenge ourselves to discover and embrace new and creative ways to deliver exceptional insight for clients.

Together we leverage a diverse network of providers and data, expert research capabilities and actionable analytics to bring remarkable clarity to life sciences’ most important decisions.

With ongoing and ground-breaking developments in Oncology and Rare Disease, an increased focus on more scientific, targeted medicine and continuous integration of technology into development and delivery of medicine, there has never been a more exciting time to work in Life Sciences and, with Cerner Enviza immersed in all of these, there has never been a better time to join us and make a difference to our clients and the lives of patients.


PRIMARY RESPONSIBILITIES

Client relationship
  • Project coordinator and key contact of communication between sponsor and investigator
  • Acts as a consultant / trusted Advisor to clients
  • Ensures the best client satisfaction and servicing to warrant client loyalty
  • Working on regional patient-centric evidence projects that cover South Korea
  • Participates in the generation of new NIS opportunities with local or APAC clients
Project
  • Management and implementation of either global or local non-interventional studies (or Phase IV research)
  • Validates study protocol, material and planning
  • Recruit and select investigators
  • Conduct site feasibility check, and selection activities for verifying adequate qualifications
  • IRB preparation, submission and closing; contract preparation and negotiation with research organizations and vendors.
  • Monitor investigator performance and adherence to protocols, followed all GCP and GPP procedures and internal SOP
  • Data management, to ensure the enrollment process and the quality of data input
  • Site initiation and monitoring
  • Prepare progress report upon requests and related materials for client meetings
  • Manage ongoing studies and maintain good relationship with clients
  • Support on research design
  • Optimizes processes and adds value throughout projects
  • Learn different type of RWE studies, such as patient-centric evidence and patient outcome research
  • Identifies the best resources / external partner for Phase IV and hybrid patient study
  • Ensures project profitability
Internal procedure
  • Follows financial procedures (Contracts, POs, internal pricing process…)
  • Complies with administrative, financial and legal / regulatory processes (such as pharmacovigilance, SOPs, and data protection)
People
  • Contribute Phase IV / IRB and knowhow to support APAC regional phase IV study that covers South Korea
  • Identify and manage vendor / resource efficiently and effectively
  • Teamwork and contribute to team spirit
Back to Description

Because It's Personal

Time: 2:57

Additional Information

Virtual Eligible Job No
Relocation Assistance Available for this Job: No

Qualifications

Basic Qualifications
  • At least 4 years related work experience or completed higher education

All employees must be legally authorized to work in the country where the position is located. Work visa sponsorship is not available for this position.


Cerner is a place where people are encouraged to innovate with confidence and focus on what is important – people’s health and the care they receive. We are transforming health care by developing tools and technologies that make it more efficient for care providers and patients to navigate the complexity of our health. From single offices to entire countries, Cerner solutions are licensed at more than 25,000 facilities in over 35 countries.

Cerner’s policy is to provide equal opportunity to all people without regard to race, color, religion, national origin, ancestry, marital status, veteran status, age, disability, pregnancy, genetic information, citizenship status, sex, sexual orientation, gender identity or any other legally protected category. Cerner is proud to be a drug-free workplace.
If you are an individual with a disability who is unable to use our online tools to search and apply for jobs, and need assistance or an accommodation in the recruiting process, please contact us by calling 866-434-1543 or by emailing CernerCareers@cerner.com.

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