Full-time
Clinical Research Associate
Competitive
Identify, assess, and initiate investigational sitesScience & PharmaceuticalPosted 29d ago
You'll complete your application on the employer's website.
← Back to jobs
Role overview
Job type
Salary
Competitive
Sector
Posted
29 days ago
Job description
Responsibilities
Identify, assess, and initiate investigational sites
Conduct feasibility, pre-study, initiation, monitoring, and close-out visits
Ensure compliance with protocols, SOPs, ICH-GCP, and regulatory requirements
Perform source data verification and ensure data accuracy and completeness
Monitor patient recruitment and support sites in meeting targets
Ensure proper reporting of adverse events and protocol deviations
Manage investigational product handling, storage, and accountability
Maintain study documentation (TMF/eTMF, Investigator Files)
Write monitoring reports and follow-up communications
Collaborate with project teams, sponsors, and site staff
Support audits/inspections and mentor junior CRAs
Benefits
Other benefits/bonuses
Opportunity to develop your professional career with an expanding and growing company
OPIS is an international CRO (Contract Research Organization) providing.
Desio, Lombardia, ITA
https://opisresearch.com
Growth Stage
Recent News
pv magazine USA
Global polysilicon market stagnates as China price rally struggles for traction
2026-09-08
China TOPCon solar module prices rise on upstream cost pressure as deals lag offers
2026-08-31
PR Newswire
Orphan Therapeutics Accelerator Expands its Network to Extend Development and Access Pathways for Ultra-Rare Disease Therapies
2026-06-24
Company data provided by
AI Tools
Customize Your Resume
Maximize your interview chances
Build Cover Letter
Make your application stand out
Analyze How Well You Fit
Understand your strength & weakness
Qualifications
Degree in a scientific field
Minimum 2 years' CRA or clinical trial monitoring experience
Strong knowledge of ICH-GCP, ISO14155, and clinical trial processes
Good English and Microsoft Office skills
Strong organizational, communication, and problem-solving abilities
Ability to work independently and in a team
Minimum 2 years’ CRA or clinical trial monitoring experience
Required skills
Clinical Trial Monitoring, ICH-GCP, ISO 14155, Clinical Trial Processes, Microsoft Office
Experience
2+ years
Interested in this role?
Apply directly on the employer's website — it only takes a few minutes.
Similar vacancies
Other roles in Identify, assess, and initiate investigational sites or Science & Pharmaceutical
Prototyping Lab Technician, Robotics
Competitive
HealthcareFull-time
San FranciscoScience & PharmaceuticalsPosted 30+ Days Ago
You will work at the cutting edge of OpenAI's robotics hardware, partnering with hardware and software teams to develop, build, test, and iterate on robotic systems. Working closely with engineers, you will build prototypes, execute experiments, fabricate fixtures, troubleshoot hardware, and help drive rapid iteration…
HealthcareFull-time
USA - Torrance (205th Street)Science & PharmaceuticalPosted 25d ago
When you join us, you’ll be part of a global team harnessing the power of scientific testing and data-driven insights to build a healthier future. Clinical Research Coordinator Imagine your future with us At ALS, we encourage you to dream big.
Clinical Research Coordinator- Cardiac MRI Center
$21.64 - $26.50
HealthcareFull-time
BIDMC East CampusScience & PharmaceuticalPosted 26d ago
When you join the growing BILH team, you're not just taking a job, you’re making a difference in people’s lives. Responsible for screening research subjects for participation in clinical research projects, enrolling research subjects onto these studies, monitoring protocol implementation, completing required forms and reporting results.