Clinical Trial Lead
Vial
This job is no longer accepting applications
See open jobs at Vial.See open jobs similar to "Clinical Trial Lead" General Catalyst.Administration
United States · Canada
Key Responsibilities
- Managing clinical operations deliverables, ensuring adherence to timelines, quality standards, scope, and financial parameters.
- Collaborating closely with the Project Manager to develop comprehensive plans, monitor resource allocation, and ensure efficient delivery of clinical site management and monitoring in accordance with contractual obligations.
- Proactively identifying risks and promptly escalating them to the Project Manager and relevant functional leads.
- Ensuring transparent communication internally and externally regarding study progress and issues, in coordination with the Project Manager.
- Developing and maintaining project-specific clinical operations plans, including Clinical Monitoring Plans, Cohort Management Plans, and Recruitment Plans, as required per project.
- Creating and managing project-specific clinical operations reference materials and tools, including study-specific forms and logs.
- Developing training materials and conducting training sessions for the clinical operations team throughout the project lifecycle.
- Providing operational oversight for site and Clinical Research Associate (CRA) deliverables, monitoring key performance indicators such as site activation, subject recruitment, monitoring visits, data quality, and currency.
- Managing CRA resourcing, site assignments, visit schedules, and serving as the initial point of contact for clinical operations and monitoring issues.
- Reviewing and approving site monitoring visit reports, while monitoring and tracking related metrics for compliance with the Clinical Monitoring Plan and Standard Operating Procedures (SOPs).
- Conducting co-monitoring visits, assessment visits, and team training sessions as necessary.
- Overseeing site management and monitoring activities across all US clinics, adapting, driving, and tracking subject recruitment plans in collaboration with sites.
- Providing protocol and study training to assigned sites, creating and maintaining monitoring visit reports and action plans.
- Eventually engaging in co-monitoring, training, and mentoring junior team members.
- Being willing and able to travel within the US as required.
WHAT YOU’LL BRING:
- Minimum of 5 years of relevant clinical research experience in a combination of research site, biotech or pharma, or CRO experience.
- Minimum of three (3) years' experience as a Clinical Trial Lead or equivalent (Clinical Trial/Study Manager) or relevant clinical operations experience at a CRO, biotech, or pharma company.
- Minimum of 2 years of experience as a Clinical Research Associate.
- In-depth knowledge of clinical trials; the ability to see the bigger picture and prioritize critical elements of success.
- Life science degree education with independent on-site monitoring experience.
- Experience in handling multiple protocols and sites across a variety of indications.
- Flexibility and ability to travel are paramount, with strong communication, written, and presentation skills.
- Must have experience in Dermatology studies.
This job is no longer accepting applications
See open jobs at Vial.See open jobs similar to "Clinical Trial Lead" General Catalyst.