LogoFresh Jobs Ahead
Lifelancer
Lifelancer
51 – 200 Employees
ConsultingHealthcareLogistics
Lifelancer is an AI-powered talent hiring platform focused on the life sciences, pharmaceutical, and IT sectors. It helps skilled professionals present their experience, discover international jobs and project opportunities, and connect with employers seeking specialized talent. For hiring teams, Lifelancer combines AI-assisted sourcing with support for hiring and payroll across multiple countries, including compliance considerations.
LinkedIn
Company Jobs

Senior Clinical Research Associate – Hybrid, Brazil

Monitor clinical trial sites across Brazil for Medpace, a global contract research organization. Review research data, regulatory compliance, and investigational product accountability.

BRBrazilHybridFull-timeSeniorEnglish RequiredPortuguese RequiredClinical Research
Google Cloud Platform

Description

  • Conduct qualification, initiation, monitoring, and closeout visits at research sites in line with approved protocols.
  • Communicate with site coordinators, clinical research physicians, and other medical staff.
  • Assess investigator qualifications, training, facilities, laboratories, equipment, resources, and personnel.
  • Compare medical records and source documents with case report form data.
  • Identify data-entry errors and promote sound documentation practices among site staff.
  • Report protocol deviations in accordance with SOPs, GCP, and applicable regulations.
  • Confirm that investigators enroll only participants who meet eligibility criteria.
  • Review and maintain required regulatory documentation.
  • Oversee investigational product and drug accountability, including inventory control.
  • Review adverse events, serious adverse events, concomitant medications, and related illnesses for accurate, protocol-compliant reporting.
  • Evaluate patient recruitment and retention at sites and recommend improvements.
  • Prepare monitoring reports and follow-up letters detailing findings, deviations, deficiencies, and compliance recommendations.
  • Complete departmental clinical research rotations and drug or device development training.

Requirements

  • A bachelor's degree in a health or science-related discipline is required.
  • At least five years of clinical monitoring experience is required; CRC experience is preferred.
  • Able to travel throughout Brazil as needed.
  • Demonstrated experience managing clinical patients.
  • Experience working with clinical protocols and case report forms.
  • Experience preparing Investigator Site File documentation.
  • Experience reconciling Trial Master File documentation.
  • Strong spoken and written Portuguese and English communication skills.
  • Submit the application in English.

Benefits

  • Comprehensive initial and continuing training through the PACE Training Program.
  • Structured CRA promotion and development ladder with potential progression into mentoring and management roles.
  • Competitive compensation.
  • Potential to earn a substantial travel bonus.
  • Mission-focused work supporting clinical research and medical therapeutics.
  • Collaborative workplace built on open communication and mutual trust.
  • Office-based setting with access to on-site mentors.
  • Defined career tracks with transparent advancement opportunities.
  • Industry-recognized onboarding and training programs.
  • Continuing education and ongoing professional development.
  • Health, wellness, retirement, and paid time off benefits.
  • Office-based work with occasional home working available for eligible roles after training.
  • Company-sponsored social activities.

Related Jobs