Senior Data Team Lead at IQVIA

Shanghai, Shanghai, China

IQVIA Logo
Not SpecifiedCompensation
Senior (5 to 8 years), Expert & Leadership (9+ years)Experience Level
Full TimeJob Type
UnknownVisa
Healthcare, Pharmaceuticals, Clinical ResearchIndustries

Requirements

  • Bachelor's Degree in Clinical, biological or mathematical sciences or related field, or nursing qualification (Required)
  • 7 years of relevant work experience including people management. Equivalent combination of education, training and experience
  • Advanced knowledge of Data Management processes and systems
  • Solid understanding of clinical drug development process and production of Data Management deliverables
  • Proven staff management skills, strong leadership, motivational and influencing skills
  • Strong organizational skills, metrics calculations, and time management skills
  • Strong verbal/written communication skills
  • Ability to work on multiple projects and manage competing priorities effectively
  • Effective mentoring and developed coaching skills
  • Ability to achieve results through proactive communication and facilitation in a matrix service delivery environment with shared accountabilities
  • Sound judgment, decision-making and problem-solving skills
  • Ability to establish and maintain effective working relationships with coworkers, managers, and clients
  • Ability to follow instructions/guidelines, utilize initiative and work independently
  • Understanding of basic Project Finance (EAC, forecasting, burn-rate monitoring and recognizing & pursuing OOS where appropriate)
  • Ability to drive business and financial results – short and long term
  • Ability to proactively evaluate risks and potential issues and seek solutions and discuss appropriately with direct reports, colleagues, and customers
  • Demonstrates good judgement in requesting input from senior staff

Responsibilities

  • Provide expert review and guidance for production of Data Management deliverables including CRF/e-CRF, database design and set-up, validation definition and programming, Data Management Plan and database deliverables to internal and external customers
  • Provide technical advice and solutions with internal and external customers to solve problems and improve efficiency
  • Ensure that staff is trained and compliant with current operating procedures and work instructions and project scope of work
  • Identify and address professional development/training needs of staff
  • Mentor staff members to develop Data Management process, system, and drug development expertise
  • Provide operational input into proposals and scope of work. Participate in proposal defenses
  • Hold at least bi-monthly meetings with direct reports to discuss project status (including timelines, delivery updates, financial aspects, potential risks, mitigation and support required), status of initiatives, team's utilization rates, training and administrative obligations, personnel issues, and career or training objectives
  • Develop and implement plans for measuring and improving employee engagement, ensuring global consistency
  • Collaborate with project leads to address work scheduling for current and projected projects, staffing needs, technological needs, and projected peak workloads, ensuring global consistency where possible. Develop and manage associated action plans to hold members accountable
  • Efficiently convey messages from leadership to direct reports and teams, as well as effectively communicate issues and opportunities up to leadership
  • Serve as the designated substitute or ensure coverage is in place for direct reports during their absence or in case of turnover
  • Attend and participate in Bid Defenses, Kick off Meetings (KOM), as applicable. Support Request for Information (RFI), Request for Pricing (RFP), and budgets, as requested
  • Participate/Support internal and external audits and inspections, as required. Ensure required staff is assigned, trained and prepared to support

Skills

Data Management
CRF
e-CRF
Database Design
Validation Programming
Data Management Plan
Mentoring
Project Management
SOP Compliance
Employee Engagement

IQVIA

Advanced analytics and clinical research services

About IQVIA

IQVIA provides advanced analytics, technology solutions, and clinical research services specifically for the life sciences industry. Their services utilize extensive data resources and technology to create connections within healthcare, allowing clients to gain insights that help speed up the development and marketing of new medical treatments. This process is facilitated by their IQVIA Connected Intelligence™ system, which offers quick and flexible insights. IQVIA stands out from competitors by focusing on patient privacy, employing various technologies to protect individual data. The company's goal is to enhance healthcare outcomes by supporting biotech, pharmaceutical, and medical device companies, as well as researchers and government agencies, in understanding diseases and advancing medical science.

Durham, North CarolinaHeadquarters
1998Year Founded
$3,526MTotal Funding
POST_IPO_EQUITYCompany Stage
Cybersecurity, Biotechnology, HealthcareIndustries
10,001+Employees

Risks

Rapid advancement of cancer vaccines may disrupt traditional clinical research models.
Proliferation of disparate technological solutions causes technology overload in clinical trials.
Generative AI technologies face challenges in adoption due to data privacy concerns.

Differentiation

IQVIA leverages advanced analytics and big data for life sciences solutions.
The company offers privacy-enhancing technologies to protect individual patient data.
IQVIA's AI Assistant provides rapid, actionable insights for healthcare and life sciences.

Upsides

Increased adoption of decentralized clinical trials enhances patient-centric study designs.
AI-driven drug discovery accelerates identification of potential drug candidates.
Expansion of telemedicine facilitates remote patient monitoring and data collection.

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