Remote CRA II - Home-Based Trials (Spain)

ICON Strategic Solutions

España

On-site

PHP 3,050,000 - 5,229,000

Full time

3 days ago
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Benefits offered by this job

Health insurance
Retirement planning
Life assurance
Employee assistance program

Job summary

ICON plc is seeking a Clinical Research Associate II to support Spain-based clinical trials from a home-based position. You will design and analyse trials, interpret complex medical data, and contribute to advancing innovative treatments.

You will conduct site qualifications, initiations, monitoring, and close-out visits, ensuring protocol adherence, data integrity, and patient safety, while collaborating with investigators and site staff to smooth study conduct.

Qualifications

  • Bachelor's degree in a scientific or healthcare-related field.
  • Minimum of 2 years of experience as a Clinical Research Associate.
  • In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
  • Strong organizational and communication skills, with attention to detail.
  • Ability to work independently and collaboratively in a fast-paced environment.
  • Willingness to travel as required (approximately 60%).

Responsibilities

  • Contributing to clinical trial monitoring activities and deliverables.
  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
  • Collaborating with investigators and site staff to facilitate study conduct.
  • Performing data review and resolution of queries to maintain high-quality clinical data.
  • Contributing to the preparation and review of study documentation, including protocols and clinical study reports.

Skills

Organizational skills
Communication skills
Attention to detail
Independent working
Team collaboration
Travel willingness

Education

Bachelor's degree in a scientific or healthcare-related field

Job description

ICON plc is seeking a Clinical Research Associate II to support Spain-based clinical trials from a home-based position. You will design and analyse trials, interpret complex medical data, and contribute to advancing innovative treatments.

You will conduct site qualifications, initiations, monitoring, and close-out visits, ensuring protocol adherence, data integrity, and patient safety, while collaborating with investigators and site staff to smooth study conduct.

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