обновлено 4 дня назад
Global Site Activation Manager (Clinical Research)
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Global Site Activation Manager (Clinical Research): Leading strategic, operational, and financial delivery of site activation activities across global and multi-regional clinical studies with an accent on regulatory submissions, site contracting, study start-up, and lifecycle maintenance. Focus on developing activation strategies, managing cross-functional delivery and risks, supporting client and bid activities, and mentoring teams.
Location: Homebased in Centurion, South Africa
Company
provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.
What you will do
- Lead strategic, operational, and financial delivery of site activation activities across global and multi-regional studies.
- Manage study start-up from pre-award through activation, including site identification, selection, regulatory submissions, ethics approvals, contracting, and lifecycle maintenance.
- Develop and execute Site Activation Management Plans aligned with study strategy and scope of work.
- Coordinate internal teams, regional stakeholders, sponsors, and external partners to deliver studies on time and within scope and budget.
- Assess regulatory landscapes, manage risks, maintain project systems and documentation, and contribute to regulatory strategy.
- Support business development, client engagement, bid defense, team mentoring, and continuous improvement.
Requirements
- Bachelor’s degree in Life Sciences or a related field.
- At least 7 years of clinical research experience, including 3 or more years in a leadership role.
- International project experience across multiple regions.
- Strong leadership, project management, strategic thinking, and problem-solving skills.
- Experience delivering projects on time, within scope, and budget while managing multiple priorities.
- Strong communication, negotiation, stakeholder management, regulatory, clinical trial, quality, and compliance expertise.
Culture & Benefits
- Homebased work arrangement.
- Cross-functional collaboration across global and regional teams.
- Opportunities to mentor team members and contribute to continuous improvement.
- Work focused on accelerating clinical study activation and the development of medical treatments.
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