Senior Project Manager
Abarca Health- Full Time
- Senior (5 to 8 years), Junior (1 to 2 years)
Candidates should possess a four-year degree or equivalent experience, along with at least two years of Project Management experience within the Clinical Trial Industry. They must demonstrate superior organizational and communication skills, working knowledge of Microsoft Office, and the ability to work independently in a dynamic, fast-paced environment while also functioning effectively as part of a team. Strong problem-solving skills and attention to detail are essential, along with the ability to travel approximately 5-10%.
As a Project Manager, the individual will review protocols, create and manage various deliverables including timelines, KOM, URS, and Communication Manuals, and ensure established timelines are met. They will facilitate issue troubleshooting, provide technical advice to other team members, and be responsible for Tier 3 on-call coverage (24/7/365). Furthermore, they will highlight the RTMS modules, conduct client meetings and training sessions, and manage the delivery of RTSM systems, including User Acceptance Testing and system setup.
Quality and regulatory software solutions provider
Veeva Systems offers software solutions for quality, regulatory, and advertising claims management, focusing on consumer products and chemical companies. Their cloud-based platform provides visibility and traceability throughout the product journey, ensuring compliance with regulations and accelerating time-to-market. Unlike competitors, Veeva has specialized expertise in both the Life Sciences and Chemical sectors, allowing them to effectively address industry-specific challenges. The company's goal is to help clients efficiently bring safe and compliant products to market.