Clinical Lead - Senior Site Activation Lead

Premier Research; United States; À distance; USD 104 000 - 128 000; Plein temps

Résumé du poste

Premier Research is seeking a Clinical Lead - Senior Site Activation Lead to join our Clinical Management team in the United States. You will partner with cross‑functional teams to drive site activation start‑up, align timelines with study objectives, and manage budgets and contractual obligations.

Responsibilities include leading site ID kickoffs, overseeing SSU and activation deliveries, coordinating country mix and site selection, monitoring risks, and providing data‑driven updates to clients

Qualifications

• Undergraduate degree in clinical, science, or health-related field or equivalent.
• Demonstrated leadership of a team in start-up or cross-functional settings.
• Experience managing timelines and budgets in clinical project delivery.

Responsabilités

• Coordinate and collaborate with functional leads to deliver site activation per contract obligations.
• Lead Site ID Kick Off Meetings and align objectives, timelines, and study start-up strategy.
• Oversee SSU and activation deliveries in line with project timeline and study projections.
• Finalize country mix and site selection with cross-functional teams.
• Escalate risks and propose mitigation strategies to ensure on-time delivery.
• Oversee CTMS data entry through activation and justify delays with contingency plans.
• Provide weekly progress updates to internal teams, clients, and upper management.

Connaissances

Leadership

Interpersonal skills

Communication

Team collaboration

Formation

Undergraduate degree or equivalent

Description du poste

Premier Research is looking for a Clinical Lead - Senior Site Activation Lead to join our Clinical Management team.

You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success.

• We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires.

• Your ideas influence the way we work, and your voice matters here.

• As an essential part of our team, you help us deliver the medical innovation that patients are desperate for.

Join us and build your future here.

What you’ll be doing:

• Coordinates and collaborates with functional leads contributing to the delivery of site activation. Organizes/oversees strategic efforts to drive quality and efficient delivery of site activations per contractual obligations.
• Leads Site ID Kick Off Meeting. Attends relevant internal and external kick-off meetings. Understands client objectives, timelines and study start-up strategy. Reviews study budget and start-up scope.
• Oversees SSU and clinical activation deliveries in alignment with the project timeline/strategy. Updates Premier Predict/ Study projections through site activation.
• Works with Project Strategist, Medical Informatics, Medical Affairs, PM, RSMs, CLs and SSU Country Leads to finalize countries mix and site selection.
• Escalates and tracks risks to PM and Sponsor, identifying mitigation strategies. Uses data to drive decisions, next steps, and enhance team communication. Proposes proactive solutions to address risks or issues impacting delivery of site activations.
• Oversees and supports CTMS data entry through site activation to ensure data quality. If forecasted timelines are not achieved, provides clear rationale for delays, contingency plan to mitigate impact, and escalates issues as soon as identified.
• Monitors and analyzes project/program site activation status and provides metrics. Provides progress updates to internal team, client, and upper management during weekly teleconferences and as needed.

What we’re looking for:

• Undergraduate degree or its international equivalent in clinical, science, or a health-related field from and accredited institution or a licensed health-care professional is preferred.
• 5 years professional experience as a CL, RSM, PM, or SSUA or other equivalent experience.
• Demonstrated ability in the leadership of a team of individuals in study start-up and across other functions.
• Understands financial aspects of the project and ensures adherence to project timelines and study budget.
• Excellent interpersonal skills and strong team player, collaborative and able to build an effective team and comfortable in customer-facing meetings like Bid Defense Meetings.
• Excellent organizational, time-management, presentation, technical, and written/verbal communication skills.
• Strong knowledge of ICH / GCP regulations.

Premier Research is dedicated to providing compensation that is fair and competitive with market standards. The annualized minimum base pay for this role is $116,000.00 USD. The actual salary will be influenced based on a variety of factors such as the candidate’s qualifications, skills, competencies, and proficiency for the role. We also offer a comprehensive benefits package, which may include health insurance, retirement plans, and paid time off.

Premier Research is proud to be an equal opportunity employer that is compliant with all federal guidelines. All qualified applicants will receive equitable consideration without regard to race, color, religion, sexual orientation, gender identity, national origin, disability or veteran status