Sr Data Team Lead

IQVIA

Ciudad de México

Presencial

MXN 929.195 - 1.393.793

Jornada completa

14 días+

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Descripción de la vacante

IQVIA is seeking a Sr Data Team Lead to manage a team of Data Management professionals. The role involves guiding deliverables, ensuring compliance, and mentoring staff while addressing project timelines and requirements. Ideal candidates will possess a Bachelor's Degree and significant experience in clinical research data management.

Formación

8 - 10 years of experience in Study Lead roles required.
Advanced knowledge of Data Management processes needed.
Strong skills in managing multiple projects and competing priorities.

Responsabilidades

Manage and support a team of Data Management professionals.
Provide expert review for Data Management deliverables.
Collaborate with project leads for staffing and scheduling.

Conocimientos

Leadership

Communication

Problem-solving

Time Management

Mentoring

Decision-making

Educación

Bachelor's Degree in Clinical, Biological, Mathematical Sciences, or Nursing

Descripción del empleo

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Job Overview

Manage and support team of Data Management professionals to efficiently produce databases that meet customer requirements.

Job Overview

Manage and support team of Data Management professionals to efficiently produce databases that meet customer requirements.

Essential Functions

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, at a minimum: project status, including timelines, delivery updates, financial aspects of the group or project, and potential risks, associated mitigation and support required; status of any initiatives that they may be involved in; the team's utilization rates; the direct report's training and other administrative obligations, such as Standard Operating Procedures (SOPs) and corporate training mandates; 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 conveying messages from leadership to direct reports and teams, as well as effectively communicating issues and opportunities up to leadership.
Might be needed to serve as the designated substitute or alternatively 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. Also ensure required staff is assigned, trained and prepared to support.

Qualifications

Bachelor's Degree Clinical, biological or mathematical sciences or related field, or nursing qualification.
8 - 10 years of Study Lead experience: Performed study work, Study Start up, Database Lock, Conduct activities and ability to guide supporting functions in day-to-day activities.
Therapeutic Area: Oncology and Hematology or Vaccines, Reumatology or Respiratory.
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 on 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. When requesting input, ensure clearly laying out the issue and required background details, articulating what support is needed; and what are the recommended actions.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

Seniority level