Associate Clinical Project Manager
Role Overview
Associate Project Leads support clinical trial delivery, liaising with clinical teams to help bring new drugs to market.
The role is part of the core project team and supports delivery of clinical studies to contractual requirements, SOPs, policies, and practices.
Clinical project management focuses on delivery, productivity, quality, financial performance, and customer satisfaction.
Associate Project Leads may run their own studies as part of their development.
Key Skills for This Role
Full Job Posting
Job overview
Associate Project Leads support clinical trial delivery, liaising with clinical teams to help bring new drugs to market.
The role is part of the core project team and supports delivery of clinical studies to contractual requirements, SOPs, policies, and practices.
Clinical project management focuses on delivery, productivity, quality, financial performance, and customer satisfaction.
Associate Project Leads may run their own studies as part of their development.
Essential functions
- Contribute to integrated study management plans with core teams or subteams.
- Deliver assigned clinical study work according to contract while optimizing speed, quality, and cost and ensuring consistent use of study tools, training materials, and standard processes.
- Set subteam objectives, communicate them, and assess performance.
- Coordinate across functions to achieve milestones and manage study issues and obstacles.
- Monitor contract progress and proactively prepare or present project information to internal stakeholders; support external stakeholder updates.
- Identify risks and contingencies and partner with project leaders on problem solving and resolution.
- Identify quality risks and issues and help plan and implement corrective and preventive actions.
- Serve as primary customer contact for small projects or as backup contact.
- Lead subteam collaboration to achieve milestones and address obstacles.
- Support project financial success, forecast opportunities to accelerate activity and revenue, and manage scope changes with the project leader.
- Identify lessons learned and implement best practices.
- Manage vendors and vendor-related activities when assigned as primary vendor contact.
Qualifications
- Associate's or bachelor's degree in life sciences or a related field required.
- At least 2 years of clinical research experience required.
- Intermediate knowledge of job-area principles, theories, and concepts, typically obtained through advanced education and experience.
- Clinical trial knowledge, including conduct and relevant research regulations, laws, and guidelines such as ICH GCP.
- Strong written and verbal English communication and presentation skills; strong problem-solving ability.
- Planning, time management, prioritization, and organization skills; able to handle conflicting priorities and changing circumstances.
- Attention to detail and accuracy; results-oriented approach.
- Good computer skills, including Microsoft Word, Excel, and PowerPoint.
- Effective collaboration and customer service skills; able to work across geographies with cultural awareness.
- Good understanding of project financials.
- Broad protocol and therapeutic knowledge is desired.
Company competencies
- The posting lists client focus, collaboration, communication, innovation, and ownership as IQVIA core competencies.
Workplace
- Hybrid role in Thane, India.
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