Senior Clinical Project Manager
Abarca HealthSalary not specified
- Full Time
- Senior (5 to 8 years)
Not SpecifiedCompensation
Junior (1 to 2 years), Junior (1 to 2 years)Experience Level
Full TimeJob Type
UnknownVisa
Life SciencesIndustries
Requirements
Candidates should possess a Bachelor's degree or equivalent experience, and a minimum of 2-4 years of experience in software Project Management, demonstrating a proven ability to understand technical concepts and learn quickly. Prior experience in the life science industry, particularly with voice (IVR), web (IWR), and mobile (IMR) platforms, is preferred, and familiarity with SQL is a plus.
Responsibilities
The Project Manager will independently lead projects of moderate to high complexity, serving as the primary client interface and maintaining exceptional client satisfaction. They will build effective partnerships with internal teams, develop and maintain project schedules, identify and manage risks and dependencies, act as a subject matter expert on client clinical study protocols, conduct end-user training, manage issue resolution for studies in maintenance, and generate reports on project health and profitability for stakeholders.
Skills
Project Management
Client Communication
Software Development Lifecycle
Stakeholder Management
Schedule Development
Risk Management
Training
Troubleshooting
Root Cause Analysis
SQL
Voice (IVR)
Web (IWR)
Mobile (IMR)
Endpoint Clinical
Provides interactive response technology for clinical trials
About Endpoint Clinical
Endpoint Clinical provides interactive response technology (IRT) systems designed for clinical trials. Their systems assist with various trial processes such as managing drug supplies, randomizing patients, and scheduling visits. These systems are user-friendly and cater to clients in the life sciences sector, including pharmaceutical and biotechnology companies. Endpoint Clinical differentiates itself by focusing on ease of use and integration with other clinical trial management systems, ensuring that clients can streamline their processes and maintain regulatory compliance. The company's goal is to enhance the efficiency and transparency of clinical trials, allowing sponsors to conduct their research more effectively.
Key Metrics
San Francisco, CaliforniaHeadquarters
2009Year Founded
$1.7MTotal Funding
DEBTCompany Stage
Enterprise Software, HealthcareIndustries
201-500Employees