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Regional Clinical Project Manager - IQVIA

IQVIA is looking for a Regional Clinical Project Manager/ Senior Consultant to join our team in Egypt.

Function: Regional Clinical Project Manager for observational and low interventional clinical trials.

Responsibilities:
  • Participate or lead teams in the design, development and delivery of consulting projects or components of larger complex projects.
  • Review and analyze client requirements or problems and assist in the development of proposals of cost-effective solutions that ensure profitability and high client satisfaction.
  • Manage the operational aspects of observational and low Interventional clinical trials and represent project delivery with the customer.
  • Produce and distribute status, tracking and financial reports for senior management.
  • Responsible for tracking financial deliverables, reporting and invoicing on projects.
  • Ensure appropriate subject recruitment plans are in place. Ensure the Site Recruitment Action Plan (SRAP), patient recruitment target and contingency plans are in place.
  • Deliver the project / program according to the quality management plan. Guide CRAs and advise on critical specific study issues.
  • Manage project set-up, maintenance and follow-up activities through ongoing tracking and review of project progress.
  • Develop the risk management plan from and coordinate clinical issue escalation and resolution with the Sponsor.
  • Develop or review study management plans.
  • Collaborate with other functional groups such as Data Management and Biostatistics, where necessary to support milestone achievement and to manage study issues and obstacles.
  • Utilize appropriate project tools and processes for the study team to support the execution of project deliverables. 

Requirements:
  • Bachelor's degree in life sciences or related field  
  • 7 years of clinical research experience, including 3 years of project management experience.
  • In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  • Proven ability to work through others to deliver results to the appropriate quality and timeline metrics
  • Proven ability to understand customer needs and appropriately influence decision making
  • Effective mentoring and training skills
  • Ability to balance operational and strategic priorities
  • Strong communication and interpersonal skills, including good command of English language
  • Effective presentation skills
  • Demonstrated proficiency in using systems and technology to achieve work objectives
  • Demonstrated proficiency at analyzing data and information to make conclusions and drive sound decision making
  • Strong organizational and problem-solving skills
  • Demonstrated ability to deliver results to the appropriate quality and timeline metrics
  • Good team leadership skills
  • Ability to manage competing priorities
  • Strong software and computer skills, including MS Office applications
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients.

We offer

  • Career development from an Analyst to a Consultant role
  • Attractive salary and benefits
  • Participating in international projects for top pharmaceutical companies
  • Various local and international trainings

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