Remote Clinical Research Associate II – Growth & Ops

Tfy

Lisboa

Remote

EUR 38,000 - 56,000

Full time

9 days ago

A complete application in a minute

Tailored resume and cover letter, ready to send.

Get past ATS filters

Benefits offered by this job

Company car
Mobile phone
Benefits package

Job summary

IQVIA in Lisbon, Portugal is seeking a Clinical Research Associate 2 to join our on-site team. You will perform site visits, support recruitment planning, and ensure compliance with ICH-GCP guidelines while coordinating with study sites and client representatives.

The role requires a university degree in a scientific field, 2–4 years on-site monitoring experience, strong MS Office skills, and fluency in Portuguese and English. Travel flexibility and a valid B-class license are expected.

Qualifications

  • University degree in scientific discipline or health care.
  • 2–4 years of independent on-site monitoring experience.
  • Very good computer skills including MS Office.
  • Excellent command of Portuguese and English.
  • Organizational, time management and problem-solving skills.
  • Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
  • Flexibility to travel.
  • Driver's license class B.

Responsibilities

  • Perform site selection, initiation, monitoring and close-out visits.
  • Support the development of a subject recruitment plan.
  • Evaluate the quality and integrity of site practices per GCP/ICH guidelines.
  • Manage progress by tracking regulatory submissions, recruitment, CRF completion, and data queries.
  • Collaborate with study-site experts and client representatives.

Skills

Portuguese language
English language
Organizational skills
Time management
Problem-solving
Travel flexibility
Driver's license

Education

University degree in scientific discipline or health care

Tools

MS Office

Job description

IQVIA in Lisbon, Portugal is seeking a Clinical Research Associate 2 to join our on-site team. You will perform site visits, support recruitment planning, and ensure compliance with ICH-GCP guidelines while coordinating with study sites and client representatives.

The role requires a university degree in a scientific field, 2–4 years on-site monitoring experience, strong MS Office skills, and fluency in Portuguese and English. Travel flexibility and a valid B-class license are expected.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Senior Clinical Research Associate, Portugal (CRA 2)
Senior Clinical Research Associate, Portugal (CRA 2)

Quadrante • Lisboa

On-site
EUR 45,000 - 65,000
Company car
Mobile phone
Attractive benefits package
Clinical Research Associate 2 - Based in Portugal
Clinical Research Associate 2 - Based in Portugal

IQVIA • Oeiras

On-site
EUR 30,000 - 50,000
Company car
Mobile phone
Attractive benefits package
Senior Clinical Research Monitor II – Global Sites
Senior Clinical Research Monitor II – Global Sites

IQVIA • Oeiras

On-site
EUR 36,000 - 52,000
Company car
Mobile phone
Benefits package
Clinical Research Associate II - Site Monitoring
Clinical Research Associate II - Site Monitoring

IQVIA • Lisboa

On-site
EUR 35,000 - 52,000
Company car
Mobile phone
Benefits package
CRA II: Onsite Clinical Monitor with Growth & Benefits
CRA II: Onsite Clinical Monitor with Growth & Benefits

IQVIA • Porto

Hybrid
EUR 32,000 - 52,000
Company car
Mobile phone
Benefits package
Clinical Research Associate 2 - Based in Portugal
Clinical Research Associate 2 - Based in Portugal

IQVIA • Lisboa

On-site
EUR 35,000 - 52,000
Company car
Mobile phone
Benefits package
Gm, Growth & Ops — Remote (Portugal-Based)
Gm, Growth & Ops — Remote (Portugal-Based)

Tfy • Lisboa

Remote
EUR 38,000 - 56,000
Company car
Mobile phone
Benefits package
Clinical Research Associate II — Portugal | Growth & Flexibility
Clinical Research Associate II — Portugal | Growth & Flexibility

IQVIA • Oeiras

On-site
EUR 30,000 - 50,000
Company car
Mobile phone
Attractive benefits package
CRA II: Clinical Trial Monitoring & Data Quality
CRA II: Clinical Trial Monitoring & Data Quality

ICON Strategic Solutions • Lisboa

On-site
EUR 40,000 - 60,000
Annual leave
Health insurance
Retirement planning
+3
Senior CRA I — Onsite Monitoring Leader
Senior CRA I — Onsite Monitoring Leader

IQVIA • Lisboa

On-site
EUR 40,000 - 58,000
Top locations