Clinical Trial Manager - Medical Affairs

ICON; Brasil; Teletrabalho; BRL 50.000 - 90.000; Tempo integral

Resumo da oferta

An established industry player is seeking a dedicated Clinical Project Manager to oversee clinical operations from site identification to database lock. This role is pivotal in ensuring the success of clinical trials, maintaining quality and integrity while coordinating with diverse teams. The ideal candidate will have a strong background in clinical trial management and a passion for driving projects to completion. With a commitment to inclusion and well-being, this company offers a supportive environment and a range of competitive benefits to enhance work-life balance.

Serviços

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Life assurance

Flexible optional benefits

Qualificações

• Undergraduate degree or equivalent in a health-related field required.
• Experience leading local/regional or global teams is essential.

Responsabilidades

• Lead and manage clinical trials to ensure compliance with regulations.
• Collaborate with internal and external stakeholders for timely execution.

Conhecimentos

Clinical Trial Management

Stakeholder Collaboration

Project Management

Regulatory Compliance

Fluency in English

Formação académica

Undergraduate degree in clinical, science, or health-related field

Licensed health-care professional

Descrição da oferta de emprego

This role is key to the success and consistency of delivery of the clinical phase of the project. Primary point of contact for clinical deliverables for both internal and external customer. Key role to manage clinical operations to highest standard and efficient performance.

Single service project manager for clinical operations. Oversight for day-to-day delivery of of the clinical portion of the project from site identification to database lock e.g. leading the clinical team, developing and managing the clinical monitoring plan, project-level site management, clinical resource assignments, ensuring compliance with ICH-GCP and any relevant regulation, ICON SOPs and all relevant protocol aspects and operational plans.

What You Will Be Doing:

• Primary point of contact to lead, manage and co-ordinate the conduct of clinical trials to close out at a country level in accordance with ICH-GCP and other applicable local regulations.
• Maintains the quality and scientific integrity of clinical trials.
• Collaborates with cross functional internal and external stakeholders to ensure timely execution, budget execution of clinical trial deliverables within the country.
• Maintains expert country, site and protocol knowledge to support sites with questions as well as build strong site relationships.
• Partners with global, local country teams and study team to provide high level country strategy, drive study progress and country level study delivery.
• Accountable for study deliverables and drives key decisions within set country.

Your Profile:

• Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (ie, registered nurse); or equivalent work experience, required.
• Experience leading local/regional or global teams.
• Experience with clinical trial project management experience. Senior or Lead CRAs looking to take the next step in their careers are welcome to apply.
• Advanced knowledge of global clinical trial management
• Fluency in local language and business English

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs
• Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
• Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others

Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

https://careers.iconplc.com/reasonable-accommodations

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.