Associate Study Start Up Manager PCD

IQVIA; São Paulo; Presencial; BRL 180 000 - 300 000; Tempo integral

Resumo da oferta

IQVIA in São Paulo seeks an experienced Site Activation and Regulatory Lead to direct site activation, maintenance and regulatory activities for clinical studies. You will shape regulatory strategy, oversee multi-regional programs and ensure compliant, timely study execution.

The role requires a Life Sciences degree and 7+ years in a scientific/clinical setting, with strong negotiation, leadership and communication skills to drive successful outcomes across regions.

Qualificações

• Bachelor's degree in Life Sciences or related field.
• 7+ years' experience in a scientific/clinical environment, including international exposure.
• Strong negotiation and communication skills.
• Excellent interpersonal and teamwork abilities.
• Proven ability to deliver results on complex projects on time and to quality standards.
• Solid understanding of GCP and ICH guidelines; regulatory writing skills.

Responsabilidades

• Direct and manage site activation and maintenance for selected studies within RSU plans.
• Oversee regulatory strategy, submissions, and authorizations across multi-regional programs.
• Coordinate cross-functional teams and maintain CTMS and project documentation.
• Provide regulatory and technical support to enable study initiation and ongoing maintenance.
• Lead risk assessment and issue resolution to ensure timelines and budgets.
• Mentor colleagues and ensure effective stakeholder communication.

Conhecimentos

Negotiation

Communication

Leadership

Project management

Regulatory knowledge

Team player

Problem solving

Risk management

Formação académica

Bachelor's degree Life sciences

Ferramentas

CTMS

Regulatory databases

Descrição da oferta de emprego

Job Overview

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, budget and resources.

Essential Functions

• Oversee the execution of Site Activation (including pre-award/bid defense activities) and/or Maintenance for assigned projects in accordance with the agreed RSU site activation strategy, adhering to project timelines. Develop, implement and maintain the Management Plan according to the Scope of Work and Project Plan, within the agreed project strategy, resolving project related issues where required. Ensure collaboration across Regulatory & Site Activation, including communication with regions and countries, to successfully deliver the agreed project scope in compliance with the RSU Management Plan. Create and/or review technical and administrative documentation to support business development and enable study initiation and maintenance, as required. Provide specialist regulatory and technical scientific support to facilitate efficient business development, initiation and maintenance of clinical trials, whilst enabling compliance with regulatory requirements. Provide overall guidance and oversight of multi-regional and multi-protocol programs during initial start-up and maintenance phase as an integral member of the study management team. Determine regulatory strategy/expectations and parameters for submissions and all necessary authorizations
• identify regulatory complexity and challenges and offer creative and practical solutions to support the bid process and subsequent execution of the site activation plan. Assess and review the regulatory landscape and contribute to the collection, interpretation, analysis and dissemination of accurate regulatory intelligence to support assigned studies and wider company, as required. Execute operational strategy/ expectations for maintenance of clinical study approvals, authorizations and review/ negotiation of contracts and essential documents. Work with Quality Management to ensure appropriate quality standards for the duration of site activation (or Maintenance, as applicable). Mentor and coach colleagues as required. Ensure accurate completion and maintenance of internal systems (with emphasis on CTMS), databases, tracking tools, timelines and project plans with project specific information. May take a lead role in developing long standing relationships with preferred IQVIA customers. Deliver presentations/training to clients, colleagues and professional bodies, as required. May be involved in activities related to monthly study budget planning and reviews.

Qualifications

• Bachelor's Degree Life sciences or related field Req
• 7 years’ relevant experience in a scientific or clinical environment including demonstrable experience in an international role. Equivalent combination of education, training and experience.
• Strong negotiation and communication skills with ability to challenge
• Excellent interpersonal skills and strong team player
• Proven ability to work through others to deliver results to the appropriate quality and timeline metrics on complex projects
• Thorough understanding of regulated clinical trial environment and in depth knowledge of drug development process
• Demonstrated proficiency in using systems and technology to achieve work objectives
• Good regulatory and/or technical writing skills
• Strong knowledge and ability to apply Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines and applicable regulatory guidelines
• Good leadership skills, with ability to motivate, coach and mentor
• Good organizational and planning skills
• Ability to exercise independent judgment taking calculated risks when making decisions
• Good presentation skills
• Proven ability to establish and maintain effective working relationships with co-workers, managers and sponsors.
• Excellent understanding of study financial management
• Proven ability to work on multiple projects balancing competing priorities

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.comIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. . Vaga Exclusiva para Pessoa com deficiência (PCD)