Senior Clinical Research Associate (Brazil)

About the Role

The day-to-day responsibilities of this role are diverse and challenging, requiring a strong understanding of clinical research principles, regulations, and protocols. You will be working closely with investigators, study coordinators, and other stakeholders to ensure that studies are conducted efficiently and effectively.

Precision for Medicine is committed to delivering high-quality services to its clients, and this role plays a key part in achieving that goal. As a Senior Clinical Research Associate, you will be expected to embody the company's values of innovation, integrity, and patient-centricity in every aspect of your work.

What You Will Do

• Independently oversee all aspects of study site management to ensure patient safety and data quality
• Manage study start-up procedures, including feasibility assessments, regulatory submissions, and investigator contracts
• Conduct site visits, including pre-study, initiation, routine monitoring, and close-out visits
• Develop and maintain good working relationships with investigators and study staff
• Provide guidance and support to junior staff members, including training and mentoring
• Collaborate with cross-functional teams, including project managers, clinical trial managers, and quality assurance specialists
• Establish, update, and maintain study-specific trial management tools and systems
• Manage and track study progress, including site performance, data quality, and patient recruitment
• Identify and mitigate risks to study integrity and patient safety
• Develop and implement corrective action plans as needed

What We Are Looking For

• Bachelor's degree in a life science or related field
• At least 5 years of experience in clinical research, with a focus on managing complex studies
• Strong understanding of clinical research principles, regulations, and protocols
• Excellent communication and interpersonal skills, with the ability to work effectively with cross-functional teams
• Ability to work independently and as part of a team, with a strong sense of initiative and accountability
• Strong problem-solving and analytical skills, with the ability to identify and mitigate risks
• Proficiency in English and Portuguese, with excellent written and verbal communication skills
• Experience with electronic data capture systems, clinical trial management systems, and other relevant software
• Certification in clinical research, such as CCRA or ACRP, is an asset

Nice to Have

• Experience working in a similar role in Brazil or Latin America
• Knowledge of local regulations and guidelines, such as ANVISA and ICH-GCP
• Experience with study start-up procedures, including feasibility assessments and regulatory submissions
• Familiarity with precision medicine and personalized healthcare
• Certification in a related field, such as project management or quality assurance

Benefits and Perks

• Competitive salary and benefits package
• Opportunity to work with a leading clinical research organization
• Collaborative and dynamic work environment
• Professional development and training opportunities
• Flexible working hours and remote work options
• Access to cutting-edge technology and resources
• Recognition and reward for outstanding performance
• Comprehensive health and wellness program
• Generous paid time off and holiday package

• Develop a strong understanding of clinical research principles, regulations, and protocols to stand out as a candidate.
• Highlight your experience working with cross-functional teams and managing complex studies in your application.
• Be prepared to discuss your approach to patient-centricity and how you embody this value in your work.
• Showcase your problem-solving and analytical skills by providing examples of how you have identified and mitigated risks in previous roles.
• Consider obtaining certification in clinical research, such as CCRA or ACRP, to demonstrate your expertise and commitment to the field.
• Research Precision for Medicine's values and mission to demonstrate your understanding of the company's culture and goals.
• Prepare to discuss your experience with electronic data capture systems, clinical trial management systems, and other relevant software.