Parexel

Clinical Trial Coordinator Regulatory - Office based (Hybrid) - Poland (Warsaw) - FSP

Parexel  •  100k - 135k/yr  •  Republic of Poland (Hybrid)  •  23 hours ago
Apply
AI can make mistakes so check important info. Chat history is never stored.

Job Description

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

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.

We are looking for a Clinical Trial Coordinator flexible office based in Warsaw (Poland) - 3 days weekly.

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.

· Collaborate with finance/budgeting representatives.

· Meeting Planning.

Skills and Education:

  • B.A./B.S. (Life Sciences preferred) or equivalent healthcare experience.
  • Minimum 1-2 years experience being responsible for coordination/ administration of clinical trials in sites or CRO or big pharma.
  • Fluent in Local Languages and business proficient in English (verbal and written).
  • Good understanding of Global, Country/Regional Clinical Research guidelines.
  • Effective time management, organizational and interpersonal skills, conflict management.
  • Effective communication with external customers (e.g., sites and investigators).
  • Able to work independently.

We will offer you

  • Premium salary.
  • Attractive benefits.
  • Medical care plan: Health, Dental & Vision.
  • Life Assurance.
  • Excellent work environment.
  • Culture of teamwork and collaboration.
  • People who motivate and face challenges together.
  • Innovative technology.
  • Excellent training.

Base Pay Range for Poland: PLN 100,000 - 135,000

Actual salaries may vary within the range based on several factors including, but not limited to education, training, experience, professional achievement, and location.

In addition to base salary, some roles may be eligible for participation in Parexel’s annual performance-based bonus plan, annual salary review and total rewards incentives.

Our talent acquisition team will provide additional details on our bonus plan or incentive programs for those eligible roles.

Join a global community where you can transform your career into a life-changing achievement.

Apply directly or contact us via email at marta.kuniewicz@parexel.com

Parexel

About Parexel

Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory and therapeutic expertise, our team of more than 21,000 global professionals collaborates with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. Our depth of industry knowledge and strong track record gained over the past 40 years is moving the industry forward and advancing clinical research in healthcare’s most complex areas, while our innovation ecosystem offers the best solutions to make every phase of the clinical trial process more efficient. With the people, insight and focus on operational excellence, we work every day to treat patients with dignity and continuously learn from their experiences, so every trial makes a difference. For more information, visit parexel.com.

Community Guidelines

Because Parexel’s social media channels are open to the general public and employees, we are not responsible for views expressed other than our own. However, we do not tolerate posts that are:

• Abusive, harassing or threatening to others.

• Defamatory, offensive, obscene, vulgar or depicting violence.

• Hateful targeting by race/ethnicity, age, color, creed, religion, gender,

sexual preference or orientation, nationality or political beliefs.

• Sexually explicit or pornographic.

• Fraudulent, deceptive, libelous, misleading or unlawful.

• Referencing criminal or illegal activity.

• Spamming.

We reserve the right to remove any comments that do not adhere to our guidelines as well as report users who violate the rules of our page.

Industry
Chemicals & Materials
Company Size
10,000+ employees
Headquarters
Raleigh, North Carolina
Year Founded
Unknown
Social Media