PSI CRO

Lead Clinical Research Associate

Lead role overseeing clinical monitoring with remote oversight; 4+ years site monitoring; English proficiency; oncology and specialized therapies preferred.

Regional Project Lead

Senior clinical trial manager with oncology experience; English proficiency; MS Office; leadership and negotiation skills.

Grants Expense Coordinator

University degree; experience with large finance datasets; grant management in international clinical research; strong English; MS Office; analytical and detail-oriented; team player.

Coordinator, Regional F&A (OOP Compiling)

Coordinator, Regional F&A

Coordinate OOP expense reconciliation and reporting; collaborate with Finance & Administration; English Bulgarian required; bachelor's in Economics/BA; 5+ years in finance/accounting; SAP experience; hybrid role in Sofia.

Central Monitoring Manager

Bachelor's degree; clinical study lead/manager experience; strong communication and leadership; English proficiency; MS Office.

Study Startup Specialist II (~Senior level)

Study Startup Specialist II

2-3 years in clinical study and site startup; Bachelor's degree in Life Sciences; fluent in Japanese and English; strong communication and organizational skills.

Full-stack Developer (AI Solutions)

Full-stack Developer

5+ years software development; Azure; PostgreSQL; Python; React; Docker; CI/CD; Jira; English; Bachelor's degree in Computer Science.

Clinical Research Associate II

Degree in Life Sciences or similar; 1 year on-site monitoring; English (B2); native Turkish; valid driver license; willingness to travel; MS Office proficiency.

Lead risk-based monitoring implementation; strong English, MS Office skills; clinical study leadership; independent leadership.

Lead and implement risk-based monitoring in clinical studies; strong communication and leadership; English proficiency; MS Office proficiency.

College/University degree; Clinical Study Lead/Manager experience; strong communication/presentation skills; leadership; English proficiency; MS Office/Excel; risk-based monitoring expertise.

Clinical study lead/manager experience; RBM implementation; English proficiency; strong communication; leadership; MS Office skills.

Experience leading risk-based monitoring, RBM platform setup, central monitoring in clinical trials, strong communication, English proficiency.

Lead centralized monitoring, RBM setup, data review, and risk reporting; English proficient; strong leadership and communication.

Medical Monitor (Board-certified, Internal Medicine)

Medical Monitor

Board-certified Internal Medicine physician with clinical trial experience and medical monitoring responsibilities.

Board-certified Internal Medicine physician with clinical research experience; strong leadership, communication, and organizational skills; proficient with MS Office.

MD with Board-certified Internal Medicine; experience in clinical research; able to coordinate with monitors, investigators and study teams; strong leadership, communication, and organizational skills; proficient with MS Office.

MD with Board certification in Internal Medicine; clinical research experience; strong leadership, communication and organizational skills; proficient in MS Office.

Clinical Trial Liaison

MD or RN or equivalent, 5+ years in Gastroenterology; Hungarian and English proficiency; MS Office; strong communication and teamwork skills.

Lead risk-based monitoring implementation; strong leadership; clinical study management; English fluency; MS Office experience.

Clinical Trials Research Nurse

RN or LPN/LVN license; experience in patient care and clinical research; knowledge of medical terminology and procedures; cardiology or nephrology experience desired.

Site Coordinator

University degree in Life Science; minimum 2 years as site coordinator; ability to work in fast-paced environment; strong communication and problem-solving skills; flexible working hours.

University degree in Life Science; 2+ years as site coordinator; strong communication; able to handle fast-paced environment.

Lead Site Coordinator

Lead Site Coordinator with clinical trial operations experience; manage teams; ensure ICH GCP compliance.

Site Management Associate

Bachelor's in Life Sciences; open to fresh graduates; administrative experience; proficient in Chinese and English; MS Office skills; highly organized and detail-oriented.

Title	Location	Date
Lead Clinical Research Associate Full Time · 4+ YOE United States · Remote	United States Remote	Apr 24, 2026
Regional Project Lead Full Time United States · Remote	United States Remote	Apr 24, 2026
Grants Expense Coordinator Full Time Tbilisi, Tbilisi, Georgia · Onsite	Tbilisi, Tbilisi, Georgia Onsite	Apr 24, 2026
Coordinator, Regional F&A (OOP Compiling) Full Time · 5+ YOE Sofia, Sofia City Province, Bulgaria · Hybrid	Sofia, Sofia City Province, Bulgaria Hybrid	Apr 24, 2026
Central Monitoring Manager Full Time Madrid or Barcelona · Remote	Madrid or Barcelona Remote	Apr 24, 2026
Study Startup Specialist II (~Senior level) Full Time · 2+ YOE Tokyo or Osaka · Hybrid	Tokyo or Osaka Hybrid	Apr 24, 2026
Full-stack Developer (AI Solutions) Full Time · 5+ YOE Madrid, Madrid, Spain · Remote	Madrid, Madrid, Spain Remote	Apr 23, 2026
Clinical Research Associate II Full Time · 1+ YOE Ankara, Ankara, Turkey · Hybrid	Ankara, Ankara, Turkey Hybrid	Apr 23, 2026
Central Monitoring Manager Full Time · $77K Vilnius, Vilnius County, Lithuania · Remote	Vilnius, Vilnius County, Lithuania Remote	Apr 23, 2026
Central Monitoring Manager Full Time · 5+ YOE Riga, Latvia, Latvia · Remote	Riga, Latvia, Latvia Remote	Apr 23, 2026
Central Monitoring Manager Full Time · 5+ YOE Tallinn, Harju County, Estonia · Onsite	Tallinn, Harju County, Estonia Onsite	Apr 23, 2026
Central Monitoring Manager Full Time Warsaw, Masovian Voivodeship, Poland · Onsite	Warsaw, Masovian Voivodeship, Poland Onsite	Apr 23, 2026
Central Monitoring Manager Full Time · 5+ YOE Milan, Lombardy, Italy · Onsite	Milan, Lombardy, Italy Onsite	Apr 23, 2026
Central Monitoring Manager Full Time · $70K Vienna, Vienna, Austria · Onsite	Vienna, Vienna, Austria Onsite	Apr 23, 2026
Medical Monitor (Board-certified, Internal Medicine) Full Time Tokyo or Osaka · Hybrid	Tokyo or Osaka Hybrid	Apr 23, 2026
Medical Monitor (Board-certified, Internal Medicine) Full Time Singapore, Singapore, Singapore · Hybrid	Singapore, Singapore, Singapore Hybrid	Apr 23, 2026
Medical Monitor (Board-certified, Internal Medicine) Full Time Taipei, Taiwan, Taiwan · Hybrid	Taipei, Taiwan, Taiwan Hybrid	Apr 23, 2026
Medical Monitor (Board-certified, Internal Medicine) Full Time Bangkok, Bangkok, Thailand · Hybrid	Bangkok, Bangkok, Thailand Hybrid	Apr 23, 2026
Clinical Trial Liaison Full Time · 5+ YOE Budapest, /, Hungary · Hybrid	Budapest, /, Hungary Hybrid	Apr 22, 2026
Central Monitoring Manager Full Time · 5+ YOE Munich, Bavaria, Germany · Remote	Munich, Bavaria, Germany Remote	Apr 21, 2026
Clinical Trials Research Nurse Full Time Plano, Texas, United States · Onsite	Plano, Texas, United States Onsite	Apr 21, 2026
Site Coordinator Full Time · 2+ YOE Wieliszew, Masovian Voivodeship, Poland · Onsite	Wieliszew, Masovian Voivodeship, Poland Onsite	Apr 21, 2026
Site Coordinator Full Time · 2+ YOE Adana, Adana, Turkey · Onsite	Adana, Adana, Turkey Onsite	Apr 20, 2026
Lead Site Coordinator Full Time · 4+ YOE Turkey · Remote	Turkey Remote	Apr 20, 2026
Site Management Associate Full Time · 0+ YOE Shanghai or Beijing · Onsite	Shanghai or Beijing Onsite	Apr 20, 2026

Activities	Clinical trial managementClinical data managementBiostatistical programmingRegulatory affairs consultingMedical writing services
Headquarters	CH
Industries	PharmaceuticalsBiotechnology
Name	PSI CRO
Employees	3,000
Type	Private
Subsidiaries	PSI Pharma Support AmericaPSI CRO UKPSI CRO GermanyPSI CRO ItalyPSI CRO France
Tagline	Manages clinical trials for the pharmaceutical and biotechnology industries.
Founded	1,995
Website	psi-cro.com

PSI CRO

About PSI CRO