Website IQVIA
Sharing a Vision to Drive Healthcare Forward Healthcare is an industry designed to help humans. As a global community, we continuously invest and commit to advancing human health. To deliver value and real outcomes. To rise to the challenge to find the next breakthrough by making the most of increa… read moresingly limited resources. We are inspired by the potential and propelled by the possibilities. We share the vision to drive healthcare forward. To see how we can help accelerate progress and achievements. Others are developing these medical breakthroughs. We do our part by using breakthroughs in insights, technology and human intelligence to reimagine and deliver ways to help make them a reality. It’s bigger than better clinical trials. Or advances in technologies and analytics. Or faster insights. It’s about exploring a new path to better health outcomes via Human Data Science. It’s about harnessing the power of the IQVIA COREâ„¢ to channel the insights, commercial and scientific depth, and executional expertise that drive maximum value for our customers. Motivated by the industry we help, we’re committed to providing solutions that enable life sciences companies to innovate with confidence, maximize opportunities, and, ultimately, drive human health outcomes forward. Southdown's Ridge Office Park 2nd Floor, Unit 5 Corner Nellmapius & John Vorster Drive Irene Ext. 54 Centurion Pretoria South Africa 0169
The Associate SAM is a fundamental role to deliver our clinical trial portfolio and belongs to a global unit with vast career growth opportunities.
Typical day to day includes working on 1-2 projects or a same client program performing the following activities:
Participation of pre award and big defense meeting activities providing start up expertise input for the project strategy.
Upon award, develop the site activation delivery strategy according to project scope and specifics, indicating the activation projection for sites in diverse countries, site identification, regulatory, contract and start up elements’ timelines.
Oversee the execution of global site activation strategy, focusing in delivering sites in the agreed timeline, budget and within scope, pro-actively identifying and addressing risks.
Communication with client, project team members and local regulatory specialists on study sites status, activation projections, risks, and opportunities to secure the activation strategy.
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
Must have a Bachelor’s Degree Life sciences or related field.
At least 3 years with 1 year of global experience in a clinical research environment.
Strong leadership competencies to lead projects and multi-cultural teams.
Project ownership controlling delivery on time, within scope and controlling budget.
Demonstrable experience working on multiple projects or clients balancing competing priorities
Strong communication skills with the ability to negotiated 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.
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