Assoc. Site Activation Manager - Sponsor Dedicated at IQVIA

São Paulo, State of São Paulo, Brazil

IQVIA Logo
Not SpecifiedCompensation
Mid-level (3 to 4 years), Senior (5 to 8 years)Experience Level
Full TimeJob Type
UnknownVisa
Clinical Research, Pharmaceuticals, HealthcareIndustries

Requirements

  • Strong leadership competencies to lead projects and multi-cultural teams
  • Project ownership controlling delivery on time, within scope
  • Demonstrable experience working on multiple projects or clients balancing competing priorities
  • Strong communication skills with the ability to negotiate and challenge decisions
  • Proven ability to work through others to deliver results to the appropriate quality and timeline metrics on complex projects
  • Proven ability to establish and maintain effective working relationships with co-workers, managers, and sponsors

Responsibilities

  • Oversee the execution of Site Activation and Maintenance for assigned projects in accordance with the agreed RSU site activation strategy, adhering to project timelines
  • Upon award, develop the site activation delivery strategy according to project scope and specifics, indicating the activation projection for sites in diverse countries within LATAM, regulatory, contract and start up elements’ timelines
  • Oversee the execution of site activation strategy, focusing on delivering sites in the agreed timeline, budget and within scope, pro-actively identifying and addressing risks
  • Communicate with client, project team members and local regulatory specialists on study sites status, activation projections, risks, and opportunities to secure the activation strategy
  • Mentor and coach colleagues as required
  • Ensure accurate completion and maintenance of internal systems and client’s system, databases, tracking tools, timelines, and project plans with project specific information
  • Direct and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including pre-award activities, oversight of the scope of work and resources

Skills

Site Activation
Project Management
Regulatory Affairs
Contract Management
Risk Management
Stakeholder Communication
Team Leadership
Multicultural Teams
Timeline Management
Budget Control
LATAM Operations
Clinical Research

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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