Investigator Site Contract Analyst (R1077357) in Seoul,SK at IQVIA™

Date Posted: 6/13/2019

Job Snapshot

  • Employee Type:
    Contractor
  • Location:
    Seoul,SK
  • Date Posted:
    6/13/2019
  • Job ID:
    R1077357

Job Description

IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.

Leads, directs and coordinates activities of a major segment of the sales organization in a large region to achieve financial and strategic growth goals across multiple accounts.

PURPOSE

Coordinate and support the delivery of all required start-up contracting activities for selected sponsors, studies or multi-protocol programs as determined by either the agreed algorithm or the Sponsor’s requirements, including pre-award activities. Provide Legal advice on contracting language. Provide support to other the Regional Investigator Contract Analysts

RESPONSIBILITIES

The role holder may be required to cover all or some of the responsibilities mentioned below but will focus on selected activities at any one time, depending on business requirements.

  • Develop contracting strategies and proposal text to support the proposal development process.
  • Develop contract and budget language templates and contracting systems, tools, processes, and training materials for selected sponsors, studies or multi-protocol programs according to the Scope of Work and Project Plan, within the agreed project strategy.
  • Ensure collaboration, including communication with sponsors, stakeholders and RSU regions and countries, to successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management Plan.
  • Provide specialist legal, operational and financial contracting support to facilitate efficient business development and initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements.
  • Create and/or review of core scientific, technical and administrative documentation to support business development and enable study initiation and maintenance, as required.
  • Assess and review the contracting landscape and contribute to the collection, interpretation, analysis and dissemination of accurate contracting intelligence to support assigned studies and the wider company, as required.
  • Ensure overall contracting efficiency and adherence to project timelines and financial goals; report contracting performance metrics and out of scope contracting activities as required.
  • Work with Quality Management to ensure appropriate contract management and quality standards. 
  • Mentor and coach colleagues as required.
  • Deliver presentations to clients as required.  Ensure accurate completion and maintenance of internal systems (with emphasis on CTMS), databases, tracking tools, timelines and project plans.
  • May take a lead role in developing long standing relationships with preferred  customers.
  • Provide legal advice to colleagues in the Asia Pacific region on Investigator Site Contractual documents
  • Provide legal advice to colleagues on country specific legal requirements in the Asia Pacific region

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

  • Good negotiating and communication skills with ability to challenge

  • Good interpersonal skills and a strong team player
  • Very Good legal, financial and/or technical writing skills
  • Understanding of regulated clinical trial environment and knowledge of drug development process
  • Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines
  • Knowledge of applicable regulatory requirements, SOPs and company’s Corporate Standards
  • Proven ability to exercise independent judgment, taking calculated risks when making decisions
  • Good Leadership Skills with ability to motivate, coach and mentor
  • Good organizational and planning skills
  • Good presentation skills
  • Strong knowledge of Microsoft Office and e-mail applications
  • Good understanding of clinical trial contract management
  • Strong legal knowledge
  • Ability to work well within a matrix team environment
  • Ability to establish and maintain effective working relationships with co-workers, managers and sponsors.
  • Fluent in Korean both written and oral

MINIMUM REQUIRED EDUCATION AND EXPERIENCE

  • Bachelor's degree in a related field and 5 years’ relevant experience, including demonstrable experience acting as a local or regional contract expert.

PHYSICAL REQUIREMENTS

  • Extensive use of keyboard requiring repetitive motion of fingers.
  • Extensive use of telephone and face-to-face communication requiring accurate perception of speech.
  • Regular sitting for extended periods of time.
  • Occasional travel.

Join Us

Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.

Forge a career with greater purpose, make an impact, and never stop learning.



Job ID: R1077357