Clinical Research Associate II/Sr
Employment Information
Report this job
Job expired or something wrong with this job?
Job Description
Clinical Research Associate monitoring clinical trial sites for Parexel, a global CRO delivering life-changing medicines. Managing site relationships, documentation, compliance, and audit readiness across studies.
Responsibilities:
- Monitor clinical trial sites through on-site and remote visits
- Build and maintain strong relationships with investigators and site staff
- Collaborate with cross-functional teams to meet project timelines
- Manage site-level study documentation, systems updates, and visit reports
- Implement corrective actions when needed to maintain study integrity
- Ensure sites are always audit- and inspection-ready
- Support high-quality clinical trial execution, site partnerships, and compliance across all phases of a study
Requirements:
- Detail-oriented and a strong problem solver
- Highly communicative, collaborative, and adaptable
- Motivated, accountable, and able to work independently
- Positive, professional, and comfortable supporting virtual and in-person teams
- Must reside in São Paulo City, Rio de Janeiro City, Curitiba, or Porto Alegre
- Must be fluent in English and Portuguese
- Bachelor’s degree in life sciences, pharmacy, nursing, or related field is required
- Minimum of 1 year of CRA experience
- Must be able to travel
- Must hold a valid driver’s license
Benefits:
- Work in a collaborative and inclusive environment that values your expertise
- Career growth and professional development opportunities
- Work-life balance
- Flexible working arrangements
- Learning is constant
- Exposure to a world of experiences and open doors
- Opportunity to work on groundbreaking clinical research projects
Similar Jobs
Lead Clinical Research Associate
Lead Clinical Research Associate overseeing country-level trial quality, compliance, monitoring, and clinical teams for PSI, a contract research organization. Providing remote study oversight across clinical research activities in Colombia.
Lead Clinical Research Associate
Lead clinical research trials for PSI, a contract research organization, across Peru and regional teams. Oversee monitors, compliance, data integrity, training, audits, and study delivery remotely.
Lead Clinical Research Associate
Lead Clinical Research Associate overseeing country-level trial quality, compliance, monitoring, and team coordination remotely for PSI, a contract research organization.
Clinical Research Associate
Clinical Research Associate monitoring early-development clinical trials for ICON, a global healthcare intelligence and clinical research organisation. Conducting site visits, ensuring ICH-GCP compliance, and maintaining data integrity and patient safety.
Clinical Research Associate II
Clinical Research Associate monitoring clinical studies for Precision for Medicine, a CRO integrating trial execution with scientific, laboratory, and data-science expertise. Coordinating site setup, regulatory submissions, initiation visits, compliance, and risk mitigation across Belgium and the Netherlands.
Clinical Research Associate II
Clinical Research Associate monitoring clinical trials in Belgium for a life-sciences CRO. Ensuring compliant site execution, study progress, regulatory submissions, and risk mitigation.
Research Specialist
Research Specialist responsible for creating client reports and market research for US Sales Enablement team. Engaging with diverse teams and mentoring junior analysts for effective project delivery.
Clinical Research Associate II
Clinical Research Associate II responsible for global study implementation in Germany. Join AbbVie to improve global healthcare managing clinical trials in a dynamic research environment.
Clinical Research Associate II – Full-time, 24-month fixed-term
Clinical Research Associate II at AbbVie leading global drug studies in Germany. Managing study execution, coordination, and compliance for clinical trials through collaborative efforts.
Compliance Research Associate
Compliance Research Associate responsible for executing research projects for the Democratic National Committee. Focused on social media research and vetting using LexisNexis databases.
Technical Research and Development Specialist – R&D
Technical Research & Development Specialist handling R&D assessments for Australian professional services firm. Engaging in technical uncertainty discovery and analysis through AI-assisted workflows.
Research Analyst
Research Analyst supporting community-engaged research, program evaluation, and quality improvement initiatives. Focus on Federally Qualified Health Centers and improving health outcomes and equity.
Quantitative Research Associate, International Development
Quantitative Research Associate supporting international development projects by managing data and conducting analyses. Collaborating with major international donors for innovative policy designs.
Senior Clinical Research Associate
Senior Clinical Research Associate managing drug trials for an innovative life sciences company. Responsible for oversight, support, and documentation throughout clinical trial processes.
Clinical Research Associate – Internal Site Management
Clinical Research Associate ensuring Good Clinical Practice compliance through site monitoring for clinical trials. Collaborating with cross-functional teams and managing site communications effectively.
In-House Clinical Research Associate
Clinical Research Associate ensuring data quality and regulatory compliance for clinical trials. Engaging with diverse teams to facilitate efficient execution of studies and support patient care.
Senior Clinical Research Associate – Oncology
Senior Clinical Research Associate managing oncology trials while leading site management activities remotely for Worldwide Clinical Trials. Collaborating on research across diverse therapeutic areas within a global team.
Investigative Research Specialist
Investigative Research Specialist focused on identifying plaintiffs for a U.S.-based employment law firm. Conducting research on California employers and verifying employee contact information.
Clinical Research Associate II, Sponsor-dedicated
Clinical Research Associate II overseeing clinical study site activities, ensuring compliance with regulatory standards in Denmark. Collaborating with site staff to optimize study performance and patient safety.
Clinical Research Associate II – Argentina
Clinical Research Associate improving clinical trial execution at Parexel. Ensuring high‑quality trial execution and compliance through site partnerships and oversight.