IQVIA Posted October 14, 2026

Clinical Research Coordinator - Mariánské Lázně

Plzeň/Pilsen, Czech Republic Part time
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IQVIA is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Site Research Assistant / Clinical Research Coordinator – Mariánské Lázně (Part-Time, 18 hours per week)

Start Date: Immediate

Duration: Approximately 6 month

IQVIA is currently recruiting a dedicated Site Research Assistant /Clinical Research Coordinator to support a clinical research site in Mariánské Lázně. This part-time position offers a unique opportunity to contribute to meaningful research in a collaborative and dynamic environment.

Key Responsibilities

As a vital member of the site team, you will help ensure the smooth execution of the clinical trial by performing a range of administrative and clinical support tasks, including:

Maintaining and updating study documentation, including protocols, case report forms (CRFs), and Electronic Data Capture (EDC) systems

Supporting patient screening and enrollment, including handling informed consent and privacy documentation

Coordinating logistical activities for study procedures in line with the study protocol

Performing data entry, quality checks, and resolving queries to ensure data accuracy and completeness

Managing and shipping biological samples

Communicating with study monitors and responding to study-related inquiries

Carrying out general administrative tasks related to the study

Your Profile

We are looking for candidates who bring a combination of education, experience, and skills:

Bachelor’s degree in life sciences or equivalent education and/or relevant experience in a clinical or medical setting (e.g., clinical research coordinator, research assistant, nurse, medical assistant)

Solid understanding of clinical trials and familiarity with study protocols, consent forms, and schedules

good knowledge of medical terminology

Strong IT skills, including proficiency in MS Office applications (Outlook, Word, Excel, Access)

Must have at least 1-2 years experience working as a Clinical Research Assistant, Research Nurse or Clinical Research Coordinator at a clinical trial site

Excellent interpersonal and communication skills

Strong organizational skills and attention to detail

Fluency in Czech and good command of English

Why Join IQVIA?

At IQVIA, you will be part of a global team that is advancing healthcare through data, technology, and human science. We offer a supportive work environment, impactful projects, and the opportunity to make a real difference.

Interested?

If this sounds like the right opportunity for you, we encourage you to apply today.

#LI-HCPN

#LI-CES

#LI-DNP

#LI-NS1

#LI-Onsite

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Job details

Seniority
Not listed
Function
Clinical Development
Therapeutic area
Not listed
Location
Plzeň/Pilsen, Czech Republic
Employment type
Part time

How this role compares

Computed from every other active Clinical Development role in our database, not just this employer's listings.

We currently track 1275 comparable Clinical Development roles across 107 biopharma companies.

1275Comparable roles tracked
1207Currently active
107Companies hiring similar roles
54Countries represented

Salary context

406 of 1275 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Lowest disclosed · Patient Safety, Medical Director · Vertex Pharmaceuticals Inc (US) $0/hr – $0/hr (≈ $0–$0/yr)
Peer group range $0 – $458,800 (median $207,850)

Where these roles are based

Top locations among the 1275 comparable roles

United States654
India131
United Kingdom75
China57
Poland32
Japan29

+ 48 more countries

Seniority mix

903 of 1275 peers have a known seniority level

Manager250
Director219
Senior143
Associate Director112
Senior Director51
Principal42
Executive/VP32
Associate30
Intern/Fellow/Postdoc24

Therapeutic area mix

189 of 1275 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology106
Immunology29
Neuroscience21
Cardiovascular / CVRM8
Respiratory8
Dermatology & Aesthetics6
Ophthalmology5
Rare Disease3
Vaccines & Infectious Disease2
Gastroenterology1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

40%similar
IQVIA Prague, Czech Republic
Same function Same country
40%similar
IQVIA Prague, Czech Republic Senior
Same function Same country
40%similar
IQVIA Prague, Czech Republic
Same function Same country
40%similar
IQVIA Prague, Czech Republic
Same function Same country
25%similar
AstraZeneca Gaithersburg, Maryland, United States of America Director
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

25%similar
AstraZeneca Gaithersburg, Maryland, United States of America Director
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

40%
CTA2- One Sponsor dedicated- Prague
IQVIA · Prague, Czech Republic · Seniority not listed
Function Therapeutic area Seniority Country
40%
Clinical Trial Submission Coordinator - Sponsor dedicated - Czech Republic
IQVIA · Prague, Czech Republic · Seniority not listed
Function Therapeutic area Seniority Country
25%
Associate Director, Clinical Research
AstraZeneca · Da'an Dist., Taipei City, Taiwan · Associate Director
Function Therapeutic area Seniority Country
25%
Clinical Research Physician - Clinical Development
Lilly · Indianapolis, Indiana, United States of America · Seniority not listed
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.