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Site Activation Specialist
IQVIA —서울
With moderate oversight and supervision, serve a Single Point of Contact (SPOC) to perform site maintenance, amendment, and site support activities, with…
Senior/Site Activation Specialist, Sponsor Dedicated
IQVIA —서울
Perform feasibility, site ID, start up and site activation activities according to applicable regulations, SOPs and work instructions.
4일

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Senior/Site Activation Specialist, Sponsor Dedicated

IQVIA -
서울

지금 지원하기

채용공고 세부정보

정규직
4일 전

상세 직무 내용

Seoul, Korea, Republic of | Full time | Hybrid | R1560872

Job Overview
Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activitie. Developing professional individual contributor who works under moderate oversight and supervision. Responsible for making recommendations for enhancements in systems and processes to solve problems or improve effectiveness of job area. Problems faced are general and may require understanding of broader set of issues but are not complex.

Essential Functions

Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary. Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project timelines.
Perform feasibility, site ID, start up and site activation activities according to applicable regulations, SOPs and work instructions. Distribute completed documents to sites and internal project team members.
Prepare site documents, reviewing for completeness and accuracy.
Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.
Review and provide feedback to management on site performance metrics.
Review, establish and agree on project planning and project timelines. Ensure monitoring measures are in place and implement contingency plan as needed.
Inform team members of completion of fesibility, site ID, regulatory and contractual documents for individual sites.
Review, track and follow up the progress, the approval and execution of documents, questionnaires, CDA/SIF, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents, in line with project timelines.
Provide local expertise to SAMs and project team during initial and on-going project timeline planning.
Perform quality control of documents provided by sites.
May have direct contact with sponsors on specific initiatives.

Qualifications

Minimum of 2 years of CRA experience or 2 years of SSI CRA experience is required.

Bachelor's Degree Life science or related field.

Experience in IRB submission, budget/contract negotiation, essential document package preparation, site activation, etc.

Responsible for SSU (Study Start-Up) activities including site selection visits, protocol review, and drafting country-specific ICF documents

Strong understanding of global clinical studies and site operational requirements, with the ability to effectively communicate between Sponsor–SSU CRA and SSU CRA–Site.

Solid knowledge of site start-up processes and overall clinical trial operations at site level

Strong English communication skills required.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Where you'll work

Hybrid

You’ll split your time between home and the office, giving you the flexibility to focus where you work best while still building strong in-person connections with your team. This model combines the autonomy of remote work with the collaboration, energy and resources of an office environment.

Culture

Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

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서울의 health specialist에 대한 최신 취업소식을 받고 싶습니다.

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Where you'll work

Hybrid

Culture

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