Clinical Research Associate, Single Sponsor

🕒 September 8

🇵🇱 Poland – Remote

💵 zł132.8k - zł280k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

👻 Ghost score 8%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

IQVIA

WebsiteLinkedInAll Job Openings

10,000+ employees

💼 Consulting

🏭 Manufacturing

📣 Marketing

💰 $1G Post-IPO Debt on 2023-05

Consulting • Manufacturing • Marketing

IQVIA is a global leader in data analytics and technology solutions, dedicated to improving health outcomes. The company utilizes its Connected Intelligence platform to harness the power of advanced data analytics and artificial intelligence, facilitating innovation in healthcare. IQVIA focuses on various areas, including clinical research, technology, and consulting services to solve complex healthcare challenges and accelerate the delivery of new therapies to patients.

📋 Description

• Perform monitoring and site management work to ensure sites conduct studies and report study data according to the study protocol, applicable regulations and guidelines, and sponsor requirements. • Perform site selection, initiation, monitoring and close-out visits. • Maintain appropriate documentation. • Support development of a subject recruitment plan. • Establish regular lines of communication with assigned sites. • Administer protocol and related study training to assigned sites. • Evaluate the quality and integrity of site practices and escalate quality issues as appropriate. • Track regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution to manage study progress.

🎯 Requirements

• Minimum of a Bachelors Degree in scientific discipline or health care. • Experience of 1 year in on-site monitoring clinical trials. • Good knowledge of, and skill in applying, applicable clinical research regulatory requirements, including Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. • Computer skills including proficiency in Microsoft Word, Excel and PowerPoint. • Ability to use a laptop computer, iPhone and iPad where applicable. • Written and verbal communication skills. • Good command of Polish and English. • Ability to establish and maintain effective working relationships with co-workers, managers, and clients.

🏖️ Benefits

• Potential incentive plans, bonuses, and/or other forms of compensation • Health and welfare benefits • Diversity and inclusion-focused workplace culture