Job Description

Location: Flexible/office based in Warsaw.

Everything we do has the potential to impact patient lives, and our Study Coordinators take their work seriously, demonstrate empathy, and act with heart. They also perform with urgency, navigating our streamlined clinical operating model to drive effectiveness, reduce handoffs and increase employee, client, and site satisfaction.

Open to Clinical Trial Assistant, Study Coordinator, Clinical Trial Coordinator , Project Support Associate, ICSM. or similar.

As a Study Coordinator, at Parexel FSP , you will be joining a team with a wide variety of experiences and knowledge. We're looking for people like you to take the initiative to do things better and smarter people who want to grow personally and professionally. We recognize and uphold the importance of all people, the way we do things, our quest for innovation, and most importantly, our patients.



Position Purpose:

The Clinical Trial Coordinator (CTC) will support the Clinical Research Manager (CRM) and other team members through the life cycle of the study from study start up to study closure.



Primary Duties:

•Trial and site administration and support.

•Regulatory & Site Start Up responsibilities.

•Budgeting, Agreement and Payments: Collaboratewithfinance/budgeting representatives.

•Meeting Planning.Qualifications

Skills and Education:

B.A./B.S. (Life Sciences preferred) or equivalent healthcare experience.

Minimum1-2yearsinClinicalResearchorrelevanthealthcareexperience.

FluentinLocalLanguagesandbusinessproficientinEnglish(verbalandwritten).

GoodunderstandingofGlobal,Country/RegionalClinicalResearchGuidelinesandabilityto

workwithin theseguidelines.

Effectivetimemanagement,organizationalandinterpersonalskills,conflictmanagement.

Effectivecommunicationwithexternalcustomers(e.g.sitesandinvestigators).

Abletoworkindependently.

About Parexel FSP:

A global provider of functional service solutions across a range of specialized disciplines for clinical development and biopharmaceutical product lifecycle support including clinical operations, biometrics, safety, regulatory, medical writing, and medical affairs.



Forresults-driven and caring individuals who want to make a meaningful difference in the world, Parexel is the CRO trusted by life sciences companies to innovate keeping patients at the center of everything we do, and where an inclusive global community helps you be your best, transforming any career into a life-changing achievement.Why Work at Parexel

There are pivotal moments in every career: Sharing new treatments. Improving processes. Delivering life-saving advances. The people who succeed are the ones who make the journey go further and faster every time. What if you had a partner to support you as you reach the next level in your professional path? A partner who believes a collaborative environment is key to achieving your goals? A partner who is dedicated to your health and wellness so you can help make a difference in the lives of millions worldwide?

That's Parexel. We're a diverse team of professionals focused on one goal: getting treatments into the hands of those who need them most. Working together, the results we bring to our clients and the opportunities we bring to our team get better with every step.

How can we help you on your journey? Find your path, and learn more on LinkedIn, YouTube, Facebook, Twitter, and Glassdoor.