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.
Fantastic opportunity for you to embed yourself in our global clinical operations team working as Study Start-up Specialist in Portugal .
Become an SSU expert managing and performing all tasks at country level associated with Regulatory, Start-Up and Maintenance.
Develop your experience working with different sponsors across a multitude of therapy areas and phases.
Your responsibilities might include :
Serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Feasibility, Site Identification and Project Leadership.
Perform Regulatory, Start-up and Maintenance activities according to applicable regulations, SOPs and work instructions.
Review, prepare and negotiate site contracts and budgets with sites.
Review, track and follow up the progress, the approval and execution of documents, including contracts, regulatory, ethics ICF and IP Release documents, in line with project timelines.
Prepare site regulatory documents, reviewing for completeness and accuracy.
Distribute completed documents to sites and internal project team member
Review and provide feedback to management on site performance metrics.
Review, establish and agree on project planning and project timelines. Ensure overall project efficiency and adherence to project timelines.
Ensure monitoring measures are in place and implement contingency plan as needed.
Where applicable, act as a Country Lead for projects and assist in pre-award activities including bid defenses, proposals and oversights of the scope of work at country level.
May act as Local Regulatory, Ethics and Contract Expert and reviewer of ICF.
May act as mentor, and prepare and deliver country-specific training, for less experienced staff.
Your rewards :
We offer genuine career development opportunities for those who want to grow as part of the organization
The chance to work on cutting edge medicines right at the forefront of new medicines development
IQVIA has access to significant data pools allowing better site selection and processes. Next generation clinical development!
Flexible conditions and an attractive remuneration package
A Bachelor's degree in a health care or other scientific discipline or educational equivalent
2 years of experience in the submission of applications, modifications and notifications of Clinical Trials to the Health Authorities (AEMPS) and site contract negotiation.
Fluency in Portuguese & English
Effective communication, organizational and planning skills
Ability to work independently and to effectively prioritize tasks
Ability to work on multiple projects
Ability to establish and maintain effective working relationships with coworkers, managers and clients.
Good command of EnglisH
We know that meaningful results require not only the right approach but also the right people . Regardless of your role, we invite you to reimagine healthcare with 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.
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