• Regulatory & Start-Up Specialist Jobs in Denmark

  • Iqvia
  • Denmark
  • Save Job
  • 5 - 8 Years
  • Posted : above 1 month

Job Description:

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Job Description Join us on our exciting journey! IQVIA is The Human Data Science Company, focused on using data and science to help healthcare clients find better solutions for their patients Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward

We currently have an exciting job opportunity as Regulatory & Start-Up Specialist, Junior RSU Specialist or Senior RSU Specialist (f/m) to work mainly in the work of contracting in our Regulatory & Start-up Department in Frankfurt or Freiburg/Br

PURPOSE

Perform tasks associated with Regulatory, Start-up (RSU) and Maintenance activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines May participate in feasibility and/or site identification activities

RESPONSIBILITIES

Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, RSU Team Lead, Clinical Operations, Feasibility, Site Identification, Project Management and CST Ensure adherence to standard operating procedures (SOPs), work instructions (WIs), quality of designated deliverables and to project timelines
Review, prepare and negotiate site contracts and budgets with sites
Distribute completed documents to sites and internal project team members
Prepare site regulatory 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
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
Perform quality control of documents provided by sites

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

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

MINIMUM REQUIRED EDUCATION AND EXPERIENCE

Bachelors Degree or apprenticeship in life science or an educational background in law or economics
For a Junior Specialist position at least a training in clinical research or law; for a Specialist role at least 3 years of regulatory start-up/submission experience, for a Senior Specialist position at least 5 years of experience
Fluent languages skills in German and 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 You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes Whatever your career goals, we are here to ensure you get there! We invite you to join IQVIA

Job ID R1055361

Profile Summary:

Employment Type : Full Time
Eligibility : Any Graduate
Industry : Consulting Services
Functional Area : Production/Manufacturing/Maintenance/Packaging
Role : Production/Manufacturi ng/Maintenance
Salary : As per Industry Standards
Deadline : 20th Jan 2020

Key Skills:

Company Profile:

Company
Iqvia

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