Clinical Lead II

61 Premier Research Poland Sp. z.o.o; Polska; On-site; PLN 226,000 - 276,000; Full time

Benefits offered by this job

Health insurance

Life insurance

Retirement plan

Paid time off

Employee assistance program

Job summary

Premier Research Poland Sp. z.o.o. is seeking a Clinical Lead II to join our Clinical Management team in Poland.

You will help biotech, medtech, and specialty pharma companies transform ideas into medicines, devices, and diagnostics while contributing to delivery strategies and site activation. The role requires oncology experience and onsite monitoring exposure, with a starting base pay of 251,000 PLN annually.

Qualifications

• Bachelor's degree, or international equivalent, in a clinical/biological, scientific, or health-related field; or equivalent work experience; 2 years as Clinical Lead.
• Prior onsite monitoring experience including Risk-Based Monitoring is preferred.

Responsibilities

• Contributes to Kick Off Meeting to align SSU and clinical delivery strategy and study budget.
• Contributes to Risk Assessment meeting to identify protocol execution or operational risks.
• Collaborates with Site Start Up to identify, approve by authorities/ethics committees and activate sites within timeline/budget.
• Plans and oversees patient recruitment and retention strategies.
• Partners with CRAs to drive site enrollment targets.
• Reviews contracts and budgets to ensure team training on obligations, timelines, and tasks.
• Collaborates with PM and Regulatory Submissions Lead to establish timelines and milestones; presents status updates on clinical deliverables.
• Works with PM and PFA to forecast clinical and SSU units and monitor overburn.

Skills

Oncology experience

Risk-Based Monitoring

Clinical delivery

Project coordination

Education

Bachelor's degree in clinical/biological/science/health field or equivalent

Job description

Premier Research is looking for a Clinical Lead II 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:

• Significantly contributes to the Kick Off Meeting to ensure a strong and aligned SSU and clinical delivery strategy and the proposed study budget aligns with execution expectations of the customer.
• Significantly contributes to the Risk Assessment meeting to identify any protocol execution risks or other Clinical/SSU operational risks.
• Collaborates with Site Start Up team to ensure sites are identified, selected, approved by authorities/ethics committees and activated within the specified timeline/budget.
• Plans/oversees patient recruitment and retention strategies.
• Partners with CRAs to drive individual site enrollment targets.
• Reviews the study contract and budget to ensure clinical team members are trained on the contractual obligations, timelines and tasks.
• Collaborates with Project Manager and Regulatory Submissions Lead to establish clinical and SSU project timelines and milestones throughout the study Plans, presents and participates in sponsor calls, representing Clinical and SSU function by providing status updates on clinical deliverables.
• Works with the PM and Project Financial Analyst (PFA) to forecast clinical and SSU units to assesses any overburn.

What we are searching for:

• Bachelor's degree, or its international equivalent from an accredited institution, in a clinical, biological, scientific, or health-related field; or equivalent work experience 2 years of experience as a Clinical Lead.
• Prior onsite monitoring experience including experience with Risk-Based Monitoring is preferred.
• This role is working within our Oncology Business Unit, so experience in this therapeutic area is required.

Premier Research is dedicated to providing compensation that is fair and competitive with market standards. The minimum annualized starting base pay for this role is 251,000 PLN. The actual salary will be influenced based on a variety of factors such as qualifications, skills, competencies, and proficiency for the role.

We also offer comprehensive benefits packages, which may include health insurance, life insurance, retirement plan, paid time off, and an Employee Assistance Program.

Premier Research is more than a company - it’s a community furthering research to improve the lives of patients in critical need. We are a diverse staff thinking creatively, challenging ideas, and solving complex problems. Our Values – We Aim High, We Work Together, We Stay Agile, We Get It Done, We Care – mirror the determination, flexibility and trust that our team embodies.

As a Premier team member, you have the power to make an impact, regardless of job title and location. Our dedication to biotech and specialty pharma is unlike any other. We provide our staff with innovative technologies and continuous learning.

Premier Research is a global clinical research, product development, and consulting company. We are dedicated to helping biotech, specialty pharma, and MedTech innovators transform life-changing ideas and breakthrough science into new medical treatments. Our team is inspired by this common purpose. Premier is a place where you can change lives, and feel rewarded and celebrated. We aim high - we will not stop until we reach our goals. And we care about each other, about our customer and partners, and, most importantly, about all the patients that we touch with our work.