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IQVIA

Runs drug trials and sells health data to pharma

Local Trial Manager - Sponsor Dedicated

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeDurham, NC, USAIn-person

About the Job

Requirements

  • A bachelor's degree in life sciences or a related field is required.
  • Two years of clinical research experience in project management or trial management are required.
  • Intermediate-level knowledge of job-area principles, theories, and concepts, typically gained through advanced education combined with experience.
  • Knowledge of clinical trial conduct and ability to apply applicable clinical research regulatory requirements, including ICH GCP and relevant local laws, regulations, and guidelines, to clinical trial conduct.
  • Broad protocol and therapeutic knowledge is desired.
  • Strong written and verbal communication skills, including a good command of English, and strong presentation skills are required.
  • Strong problem-solving skills are required.
  • Planning, time-management, and prioritization skills are required, as is the ability to organize resources, set objectives, provide clear direction, and plan ahead while accounting for changing circumstances.
  • Ability to handle conflicting priorities is required.
  • Attention to detail and accuracy, and a results-oriented approach to delivery and output, are required.
  • Good software and computer skills are required, including Microsoft Office applications such as Word, Excel, and PowerPoint.
  • Ability to establish and maintain effective working relationships with coworkers, managers, and clients, and strong customer-service skills, are required.
  • Ability to work across geographies with awareness and understanding of cultural differences is required.
  • A good understanding of project financials is required.
  • Ability to demonstrate IQVIA competencies in client focus, collaboration, communication, innovation, and ownership is required.

Responsibilities

  • Provide input into the development of integrated study-management plans with the core project team and/or sub-team.
  • Be accountable for assigned portions of clinical studies under contract, optimizing speed, quality, and cost of delivery while ensuring consistent use of study tools and training materials and compliance with standard processes, policies, and procedures.
  • Set objectives for project sub-teams according to the agreed contract, strategy, and approach; communicate and assess performance.
  • Collaborate with other company functional groups as needed to support milestone achievement and manage study issues and obstacles.
  • Monitor progress against contract and proactively prepare and present project and/or sub-team information to internal stakeholders; support the project leader in proactively preparing and presenting information to external stakeholders.
  • Identify positive and negative risks and contingencies, and partner with the project leader on problem-solving and resolution efforts.
  • Achieve project quality by identifying quality risks and issues, responding to issues raised by project sub-team members, and partnering with the project leader to plan and implement appropriate corrective and preventive action plans.
  • Serve as the primary customer contact for small projects or as a backup project contact, as needed.
  • Lead a project sub-team and manage cross-collaboration to support milestone achievement and address issues and obstacles.
  • Support the project leader in ensuring the financial success of the project.
  • Forecast and identify opportunities to accelerate activities and bring revenue forward in partnership with the senior project leader.
  • Identify changes in scope and partner with the project leader to manage the change-control process as needed.
  • Identify lessons learned and implement best practices.
  • Serve as the primary vendor contact when assigned, leading project vendor management and related activities according to project requirements.

Desired Qualifications

  • Broad protocol knowledge and therapeutic knowledge are desired.

About the Company

IQVIA

Runs drug trials and sells health data to pharma

IQVIA runs clinical trials for drug, biotech and medical device companies and sells them the health data, software and analytics they use to develop and market treatments. Its research arm designs studies, recruits trial sites and patients, and manages trials through to regulatory filing. Its commercial arm sells market data, consulting and software that pharma sales and marketing teams use to plan product launches. Clients pay through multi-year service contracts and data and software subscriptions. IQVIA was formed in 2016 when clinical research firm Quintiles merged with health data company IMS Health, and it is based in Durham, North Carolina.

Company size
10,001+
Company stage
IPO
Headquarters
Durham, NC
Founded
1998

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