Clinical Project Manager

Lightship

89d • $110,000 - $145,000

About The Position

Lightship is a clinical trials service provider leading in increasing access and choice in taking part in research to improve equity for all. We design and conduct studies in partnership with biopharmaceutical companies to accelerate bringing new therapies to market. Our approach is to engage people where they are and support them across their journey in a clinical trial, from first contact to study completion. We work to make it easy, convenient, and safe for people to take part by offering visits in clinic, at home, using our mobile research units, and digital health tools. By transforming the way, we conduct clinical research, we can decrease study timelines and reduce dropouts to accelerate development of better therapies. A successful candidate will possess a willingness and desire to work independently without significant supervision. Lightship expects each individual to anchor their availability in the standard operating hours for their geographic location, however, true to our values of inclusion and flexibility, this role, along with all others at Lightship, may be asked to flex work hours to accommodate US West Coast, US East Coast, and UK-based time zones, based on business need. In practice, this may translate to days that have a slightly earlier start or evenings that have a slightly later end. Culturally, we aim to balance the ability to operate across time zones with respect for each individual's daily life. Given Lightship’s distributed model and the semi-remote nature of this position, the Clinical Project Manager possesses a willingness and desire to work independently. Additionally, this position will be brought in for a 6 month duration and will require travel during working hours, and occasional overnight travel – approximately 30%.

Requirements

• Highly developed spoken and written communication skills, excellent presentation skills.
• Knowledge/expertise in the applicable regulations/guidelines for, and the conduct of clinical trials (virtual/DCT trial experience preferred).
• Experience using a Clinical Trial Management System (CTMS) platform or equivalent.
• Strong interpersonal, collaboration and time management skills.
• Ability to establish and maintain effective working relationships with project team members, other cross functional stakeholders, and clients.
• Proactive, innovative problem solver with good analytical and critical thinking skills to appropriately anticipate and manage risks before they turn into issues.
• Ability to influence stakeholders at all levels with confidence and adapt style to deliver messaging.
• Able to work in a fast-paced, evolving environment.
• Ability to embrace and manage change, be agile and adaptable.
• Able to work independently with minimal guidance in an unstructured environment.

Nice To Haves

• Undergraduate, health-related degree OR an equivalent combination of education, training, and experience sufficient to successfully perform the key responsibilities of the job.
• 5+ years of relevant clinical research experience and solid knowledge and understanding of clinical project / trial management.
• Experience working in a CRO, Site, SMO or Sponsor preferred.

Responsibilities

• Leading cross-functional teams and third parties/vendors to ensure successful project delivery.
• Overseeing clinical research conduct, including study start-up, enrollment, execution, and close-out.
• Acting as liaison with the client and managing client contractual, organizational and relationship needs/expectations, related to operational delivery of assigned projects.
• Managing project contractual deliverables and modifications, and preparing and delivering study-related updates, dashboards and reports to study teams, senior management, and sponsors / vendors / partners.
• Ensuring project management systems are updated weekly to reflect accurate project status.
• Serving as a point of escalation for project team members.
• Ensuring project resources are appropriately assigned in project management system and updating forecasted project hours per resource to accurately reflect project needs.
• Participating in revenue forecasting and review of project actual unit/hours efficiency against budget.
• Identifying and managing scope changes with the client with support of the project Director.
• Ensuring Director and Client Partner are kept informed of project progress through the provision of appropriate and regular updates.
• Developing operational plans (including operational guidelines, manuals and project plans as needed).
• Overseeing all operational aspects of assigned clinical studies in accordance with local regulations, ICH GCP guidelines, SOPs, and project specific plans.
• Coordinating IRB/IEC correspondence and communication, ensuring that all approvals are obtained as required.
• Overseeing that study supplies and equipment are procured and delivered to patients and/or sites.
• Organizing / ensuring that appropriate study training is delivered, and maintaining the project specific training matrix and ensuring project team compliance with project specific training.
• Ensuring that the necessary technological solutions are designed and configured per study specifications.
• Ensuring that the vendors / personnel needed for each study are prepared, available, and trained, and managing assigned vendors as necessary.
• Working with study monitors to address issues and provide resolutions.
• Acting as the main point of contact for study investigator, study personnel, and sponsors / vendors / partners to ensure smooth communication and collaboration.
• Supporting Study Start-Up with the coordination of site contracts.
• Working with Legal to implement vendor contracts.
• Working with Quality to identify and mitigate risks.
• Working with Finance to ensure accurate and timely invoicing to sponsors and tracking and payment of invoices from investigators and vendors.
• Preparing requisite project status updates in keeping with project plans at a set cadence, and tailoring messaging as necessary for different internal and external audiences.
• Organizing and leading study team meetings, and meetings with sponsors / vendors / partners as applicable.
• Participating in the development, review, and implementation of standard operating procedures, manuals, tools, and training materials.
• Identifying and documenting lessons learned and best practice throughout each project, and sharing at a functional and departmental level.
• Supporting audits and inspections, as required.
• Ensuring adherence to company SOPs, policies, and guidelines at the project-level.
• Acting as a subject matter expert or Business Process Owner (BPO) for clinical systems, where assigned.

Benefits

• Top notch healthcare (medical, dental, and vision) for you and your family.
• A 100% 401(k) company match for up to 4% of eligible contributions with an immediate vesting.
• Company provided laptop, your choice of a PC or a Mac.
• Monthly stipend for internet and phone expenses.
• Short & long-term disability.
• Life insurance and More!

What This Job Offers

• Career Level: Mid Level
• Education Level: Bachelor's degree
• Number of Employees: 51-100 employees