Study Management Specialist , Allergan Aesthetics (New Created Role)

PRIMARY FUNCTION/OBJECTIVE 
Manage and lead a project on all aspects of design planning startup conduct analysis reporting and 
closeout of assigned NIS including regulatory PMOS IIS and medical operations. Responsible for managing 
planning timelines milestone budget study sites vendors and deliverables while maintaining quality and 
compliance. Also SMS will contribute to the pre-launch medical affairs initiative from medical operation 
perspective.

CORE JOB RESPONSIBILITIES 

• Provide comprehensive input to study concept development especially operational points of view. 
• Develop study protocol/protocol amendment and CRF and get approval from GUS-RC or ARC and MFDS (if 
• applicable) by managing multidisciplinary assessment. 
• Develop and provide official answers to MFDS by collecting and analyzing reference/data regarding 
• supplementary comments from MFDS (protocol annual report re-examination report) for regulatory PMOS. 
• Review and finalize CSR according to SOP and local regulation by coordinating and complying with all 
• internal processes and approvals as well as MFDS. 
•  MFDS point of contact: Communicate/Negotiate with MFDS on protocol/protocol amendment study 
• implementation or issue for regulatory PMOS
• Study project management: Accountable for all aspects of project management including study plans operation coordination timelines problem identification and resolution communication with stakeholders status reports and budget forecasting/planning CRO management to reach the milestone and to ensure timely delivery of completed study reports. 
  o Responsible for supervising daily operations and management of activities associated with assigned 
  project(s) from concept to completion of final study report and ensure project goals are achieved. 
  o Lead project start-up activities such as vendor evaluation bidding selection set-up and training as well as study site evaluation and selection 
  o Manage and steer vendors including CROs to perform studies as planned. 
  o Acts as a liaison with internal and external stakeholders regarding study update issue escalation study specific information etc. 
  o Develop study budget plan forecasting review reconciliation. Manage project specific budget by monitoring and adjusting current study status as well as evaluating FMV and ensuring investigator payments occur in a timely/compliant manner. 
  o Ensure effective project plans are in place and lead the project proactively with relevant stakeholders communication and to set priorities in accordance with applicable project plans.
• For IIS (Investigator Initiated Studies)/ IIP (Investigator Initiated Publication) manage and oversight as an 
  operational point such as coordinate and support concept/protocol review and approval from All kinds of 
  Review Committee (Affiliate Global Area) FMV assessment managing agreements documents milestones 
  (progress) payments and issues 
• Assist in the initiation oversight and follow up of assigned clinical studies and medical projects initiated 
  within the therapeutic area for which the SMS carries responsibility (e.g. post marketing clinical activities such 
  as epidemiological surveys post-authorization studies (phase IV). All such activities must comply with 
  applicable local laws guidelines codes of practice SOPs and AbbVie R&D (GPRD) SOPs. 
• Assure full compliance with GCP Global & local SOPs and Korean regulations. 

Qualifications :

• University degree or equivalent; preferably in a medical/science-related field or equivalent work 
• experience in a scientific or health-related field 
• Minimum 3-5-year experience in clinical research in healthcare pharmaceutical and/or CRO industry or 
• minimum 2-year direct experience as a project manager 
• NIS experience is preferred. 
• Experience in pre-launch launch and post-launch phases of a new product or indication. 
• Fluent English communication skills (Reading writing speaking) 
• Good understanding of clinical trial processes AbbVie internal processes and the regulatory environment  as well as strong knowledge of clinical research practices local regulations and ICH guidelines 
• Familiarity with AbbVie policies & procedures and local SOPs 
• Strong computer/technology skills including MS Word MS Excel and PowerPoint 
• Fluent English communication skills (Reading writing speaking) 
  Possess strong project management time management and coordination skills with good organizational leadership negotiation and interpersonal skills 
• Strong analytical and problem-solving capabilities with sense of responsibility 
• Manage conflict challenges decision making and risk management as a project manager 
• Ability to manage time/prioritize multitask work independently self-motivated and follow through with assigned tasks 
• Excellent written and verbal communication skills demonstrated by the ability to present clear messages 
  from complex information/data to internal/external stakeholders 

Additional Information :

AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. 

US & Puerto Rico only - to learn more visit  & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:

Work :

Yes

Employment Type :

Full-time