Senior/Site Start Up Associate II

Premier Research is looking for a Site Start Up Associate / Senior Site Start Up Associate to join our Study Start Up 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 Built for You. 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. 
We are Built by You. Your ideas influence the way we work, and your voice matters here. 
We are Built with You. As an essential part of our team, you help us deliver the medical innovation that patients are desperate for. 

 

Together, we are Built for BiotechSM. Join us and build your future here.

Proactively forecasts submission/approval timelines and ensures they are adhered to. If forecasted timelines are not reached, provides clear rationale for delays, provides contingency plan to mitigate impact, and escalates the issue as soon as identified

Local Clinical Trial Applications Specialist - may serve as the primary point of contact for the Project Manager, Clinical Manager, Clinical and Regulatory Start-up Lead (or designee) during start-up on allocated projects.

Prepares and submits Central EC/IRB Applications, Local EC Applications, RA Applications, and other local regulatory authorities or hospital approval submissions as required.  Prepares ongoing submissions, amendments, and periodic notifications required by central and local EC and RA.

Performs essential document collection and review, ensuring that sponsor and investigator obligations are being met and are in compliance with applicable local regulatory requirements and ICH/GCP guidelines.

Local Investigator Contract and budget negotiator - produces site-specific contracts from country template.  Submits proposed contract and budget for site.  Negotiates budget and contract with site and via Contracts Lead with Sponsor until resolution of issues and contract execution.

Provides all regulatory documents and relevant study correspondence along with translations to study maintenance at end of start-up.

Collects information on submission deadlines and timeline metrics for Regulatory Authority, Ethics Committees, Investigational Review Boards and other local bodies as appropriate.

Liaises with internal team members to review areas that impact study start-up and shares start-up information with the project team.

Works within the scope of Clinical Management Plan (CMP), study processes, ICH-GCP and/or ISO14155 and any other requirements mandated by the study.

 

At least 2 years’ experience in the submission of clinical trial applications.

Undergraduate degree or its international equivalent in a clinical, science, or health related field from an accredited institution or a licensed healthcare professional

Fluency in Finnish and English

Expertise in ICH/GCP and/or ISO14155 requirements as well as detailed knowledge of the relevant country specific regulatory requirements for conducting clinical

Knowledge of site and institution specific contract requirements

Authority submissions, EC submissions, notifications to data protection authorities, notifications/applications to any other local/federal/national body

 

 

Premier Research is more than a company – it’s a community of people that truly care about one another, about our clients, and about our mission of furthering research to improve the lives of patients in critical need.  

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 opportunities so that they have the tools they need to be successful. 

Because we are transforming life-changing ideas into new medical treatments for a diverse population, we require the perspectives of a diverse staff thinking creatively, challenging ideas, and solving complex problems fearlessly.
 
Through a commitment to diversity, equity, inclusion, and empowerment, we create a community of belonging that welcomes differences, fuels innovation, and better connects us to the patients, physicians, and customers we serve.  
 
We hire people that add to our culture, then invest in developing skills and abilities. If you are excited about this role, but your past experiences do not perfectly align with the position as described, we encourage you to apply anyway. You may be exactly the right candidate for this role or others. 

 

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