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[노보노디스크제약] Real World Evidence Associate 모집 (1년 계약직)

등록일자 : 2022-04-26 조회수 : 6149

Position’s key accountabilities

- Support execution and implementation of non-interventional studies and other Real-World Evidence generating studies to support the NNPK evidence generation plan with partners and with vendors.

- Contribute to driving innovation in RWE analytics by implementing new analytic methods, study design and technologies to answer research and business questions.

- Support conducting RWE studies using internal and external real world data to generate unique disease insights and epidemiological information to improve patient care and support business needs.

- Communicate RWE matters with key internal stakeholders and scientific community.

Nature and scope of Main accountabilities

- Collaborate with external vendors on RWE projects and manage communication, contracting and project follow up with external vendors (ex. CROs) and ensure expected deliverables and meet timelines / challenges on content for low or medium complexity projects.

- Identify Real World Data sources (electronic medical records, registry database, patient reported outcomes survey, and national claims database) which best support business needs through literature reviews and desk research etc.

- Able to interpret, understand and discuss data results, protocol, SAP, NSR and other study related materials, and collaborate with internal stakeholders and external vendors with timely and efficient communications.

- Collaboration in study operations with RWE manager

- Provide input for feasibility and operation perspectives to study outline

- Prepare study protocol, informed consent and amendments, if applicable

- Provide input to study and project related documents (e.g. CRF, NSR, Study Validation Plan)

- Ensure availability of other study related documents, e.g monitoring guidelines

- Plan and conduct investigator meetings and other meetings incl. Investigator Result meeting(s)

- Ensure audit and inspection readiness

- Handling protocol deviations (if applicable) to ensure high compliance

- Ensure compliance with all existing applicable requirements, and overall ensuring compliance with GCP and other applicable external regulations for the non-interventional studies as well as Criteria for medical drug promotion and local regulations in the local meetings within and outside the study community.

- Background knowledge of industry trends and best practices specifically related to epidemiology/outcomes research.

- Good knowledge and understanding of applicable regulations in pharmacoepidemiology, pharmacovigilance and clinical development.

- Conduct literature reviews and online research to support Real World Evidence projects.

- Combination of strong methodological quantitative knowledge, strategic, innovative thinking, and communication skills.

- Prepare presentation materials (in PowerPoint) and assist in document development (in Word & Excel) for Real World Evidence protocols, reports, manuscripts, posters, etc.

[자격요건]

- Degree in statistics, public health, or other health related fields.

- Master’s degree in a field such as epidemiology, biostatistics, statistics, bioinformatics, economics or similar is preferred.

- Minimum of two to three years of related experience conducting research in the pharmaceutical industry, contract research organization, healthcare provider / HTA or academic institute; or experience in a closely related discipline within the pharmaceutical industry.

- The ability to develop understanding of retrospective and prospective research methods, late phase study designs, HEOR and related methodology.

- Record of publications in observational research is a plus. -Experience working with longitudinal RWD (e.g., claims, electronic health records, and/or surveys).

- Experience in the conduct of non-interventional study, late phase study, or database study.

- Experience in using statistical software (e.g., R, SAS, Python, SPSS, and/or Stata).

- Collaborative approach to problem-solving and ability to plan and multi-task.

- Excellent written and oral communication skills.

- Excellent communication, presentation, interpersonal skills, both written and spoken.

- Proficiency in Excel, Word and PowerPoint.

- Fluency in written and spoken English.

※ Kindly upload your CV to our online career page (click on Apply and follow the instructions).

https://careers.novonordisk.com/job/Seoul-Real-World-Evidence-Associate-Seou/794804401/

※ Deadline Until the completion of recruitment. Applications will be screened on an ongoing basis, so you are encouraged to apply as soon as possible.

이전글 [노보노디스크제약] Medical Manager, New Therapy Areas Clinical Development 모집 2022.04.28

다음글 [노보노디스크제약] Sr. Regulatory Affairs Associate - 경력직 (정규직) 채용 2022.04.20

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[노보노디스크제약] Real World Evidence Associate 모집 (1년 계약직)