Senior Clinical Research Associate


Place of work
Remote work
Contract type
Wage (gross)
87 500 Kč/month

Information about the position

Job description, responsibilities and duties

We are currently looking for a Senior Initiation Clinical Research Associate to be based in our office in Prague, Czech Republic or homebased anywhere in Czech Republic.

Your time here:
At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor. CRA’s are accountable for using their expertise to build and maintain the site relationship and ensure they’re set up for success. As the clinical sites’ sole point of contact, this includes addressing and resolving site issues and questions. You’ll also manage site quality and delivery from site identification through to close-out.
As a CRA, Parexel will offer you world class technology and training catered to your individual experience. You can anticipate less travel and a lower protocol load in comparison to industry peers. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical research. If impact, flexibility, and career development appeal to you, Parexel could be your next home.

What you’ll do
• Leverage your expertise. Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV) and termination visits (TV) at assigned clinical sites and generate visit/contact reports.
• Build relationships. Oversee integrity of the study and utilize problem-solving skills to promote rapport with the site and staff.
• Protect patients. Review the performance of the trial at designated sites, ensure the rights and well-being of human subjects are safeguarded and are in accordance with protocol.
• Drive productivity. Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines, while also ensuring compliance with the approved standard operating procedures (SOPs), protocol/amendment(s), GCP, and the applicable regulatory requirement(s).
• Ensure quality. Evaluate the quality and integrity of the reported data, site efficacy and drug accountability.
• Execute. Monitor the completeness and quality of Regulatory Documentation and perform site document verification.

More about you
On your first day we’ll expect you to have:
• Substantial Site Management experience or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology.
• The ability to function as a mentor and role model for other CRAs.
• Bachelor’s or equivalent degree in biological science, pharmacy or other health related discipline.
• Strong interpersonal, written, and verbal communication skills within a matrixed team.
• Experience working in a self-driven capacity, with a sense of urgency and limited oversight. A client-focused approach to work and flexible attitude with respect to assignments/new learning.
• The ability to manage multiple tasks, evaluate a variety of unpredictable scenarios and achieve project timelines while being able to apply your understanding of study protocol(s).
• An honest and ethical work approach to promote the development of life changing treatments for patients.
• Strong computer skills, including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS) and MS-Office products such as Excel and Word.

Employee perks, benefits

A little about us
Parexel is proud to be a leading Clinical Research Organization with colleagues across the globe. As a member of our team, you’ll get to know your coworkers on a personal level. Have a question? A clinical research leader, project team member, technology “super user” or collaborator are a phone call away. Our clinical research teams meet regularly to have discussions in an open environment, allowing our team members to share their expertise and promote learning within the team. Management supports and encourages career growth through consistent performance discussions and evaluations. Whether your interest is to progress into a more senior level role, into line management, Quality, Project Leadership or a variety of other positions, Parexel prides itself on career opportunities for our employees.

• Global Impact - We are one truly global team working together to propel each client´s journey ahead faster.
• Balance - We value work-life balance. We try and keep regular hours and an emphasis on life outside the office.
• Collaboration - Work with industry leaders and subject matter experts.
• Freedom - The ability to innovate, ask “what if” and try new solutions without fear of failure.
• Variety - Opportunities to work on multiple accounts – never boring!
• Compensation - Competitive salaries and bonus structure based on individual metrics.

Requirements for the employee

Candidates with education suit the position

University education (Bachelor's degree)

Educational Specialization

or equivalent degree in biological science, pharmacy or other health related discipline.

Language skills

Czech - Proficiency (C2) and English - Advanced (C1)


Brief description of the company

Parexel is in the business of improving the world’s health. As a leading global clinical research organization (CRO), we provide a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic, technical, and functional ability is underpinned by a deep conviction in what we do. We believe in our values; Patients First, Quality, Respect, Empowerment & Accountability.

Headquartered near Boston, Massachusetts and in Durham, North Carolina, and supporting clients in more than 100 countries, our almost 16,000 employees are united by one simple fact. We care. We’re not just the people with brains, we’re the people with heart.

Number of employees

1000 and more employees

Company address

Parexel International
101-105 Oxford Road
UB8 1LZ Uxbridge
Great Britain


Kontaktní osoba: Diane Correia
E-mail: poslat životopis
ID: 4111386  Datum zveřejnění: 25.6.2021  Spodní hranice mzdy (brutto): 87 500 Kč/month