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IQVIA

Runs drug trials and sells health data to pharma

Compliance Senior Consultant

Risk, Regulatory & Legal AdvisoryConfirmed live in the last 24 hours
Full-timeWarsaw, PolandPLN206.9k - PLN384.1k /yrIn-person

About the Job

Requirements

  • A minimum of 4–6 years of strategic management consulting or legal experience is required, preferably with a Big 4 firm, strategy consulting firm, specialized healthcare consulting firm, or law firm.
  • An undergraduate degree or equivalent experience is required.
  • A track record of delivering projects on time and on budget is required.
  • Strong written and verbal presentation and communication skills are required.
  • Candidates must be organized, self-motivated, and able to work independently.
  • Candidates must be analytical and quantitative, comfortable with numbers, and have strong business acumen and leadership skills.
  • Candidates must be willing to express differing opinions and articulate thoughts and concepts clearly.
  • Candidates must be willing and able to improve skills related to IQVIA core competencies.
  • Candidates must be willing to travel.
  • Candidates must submit their CV in English.

Responsibilities

  • Support and lead consulting projects.
  • Lead clients in business workshops and interviews.
  • Develop project deliverables, which may include data analyses and reports, process reviews and assessments, policies, and standard operating procedures.
  • Develop, articulate, and present ideas and opinions.
  • Manage projects and take accountability for them.
  • Provide mentorship for junior staff members.
  • Develop relationships with clients and identify future opportunities.
  • Create project deliverables with some oversight from senior staff.
  • Support the growth of the organization.
  • Perform other duties as assigned.
  • Develop and present project plans and proposals.
  • Serve in a largely client-facing role and potentially act as the day-to-day client contact on projects.
  • Oversee deliverables, timelines, and ongoing project execution.
  • Conduct quality reviews of staff deliverables.
  • Work on special and internal projects as assigned by Engagement Managers and Principals.

Desired Qualifications

  • An MBA, a law degree (JD or equivalent), or another master's degree is preferred.
  • Experience or knowledge of the pharmaceutical industry, particularly compliance and risk management issues, is a strong plus.

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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