Clinical Research Associate – FSP

Parexel

Clinical Research Associate managing oncology studies and supporting a single client at Parexel in Poland. Responsibilities include site management and mentoring junior CRAs with opportunities for travel and remote work.

Posted 7/16/2026full-timeRemote • 🇵🇱 PolandJuniorMid-Level💰 PLN 220,000 - PLN 240,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates extensive experience in site management and independent site monitoring within oncology trials, with a strong understanding of clinical trial methodology, GCP/ICH guidelines, and effective problem-solving and organizational skills.

Highest-signal resume keywords

Site ManagementIndependent Site MonitoringClinical Trial MethodologyOncology TrialsGCP/ICH Guidelines

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Clinical Trial MethodologySite ManagementIndependent Site MonitoringOncology TrialsClinical Research Knowledge

Soft Skills

Effective Time ManagementOrganizational SkillsInterpersonal SkillsProblem-Solving Skills

Industry Keywords

Clinical Trial PhasesGCPICHClinical Research LegislationOncology

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

You will be dedicated to a single client.
You will be responsible for all site management and supervisory activities in the assigned oncology studies.
You will work with industry leaders and subject matter experts.
You will have the opportunity to mentor junior CRAs.
You will work with world-class technology.
You will have great opportunities to travel, work from home, meet new people and play a key role in the drug development process.

Requirements

What you’ll need

Extensive experience in site management, with knowledge of clinical trial methodology and terminology.
Minimum 1 year experience in independent site monitoring of all types of visits.
Science education is a must.
Willing to work on oncology trials.
Effective time management, organizational and interpersonal skills and problem-solving skills, with the ability to multi-task and priorities.
Good understanding and working knowledge of clinical research, clinical trial phases, current GCP/ICH and country clinical research legislation and guidelines.

Benefits

Comp & perks

Premium salary
Attractive benefits
Car or car allowance
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