When our values align theres no limit to what we can achieve.
At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us no matter what we do at Parexel contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally we do it with empathy and were committed to making a difference.
At Parexel we are a leading Clinical Research Organization (CRO) specializing in delivering lifechanging medicines to patients. We are seeking a Clinical Research Associate (CRA) to join our team. As a CRA youll be joining a fastpaced driven environment thats helping to make a lifechanging difference to patients by ensuring highquality clinical trial execution building strong site partnerships and maintaining compliance across all phases of a study. Through the collaboration and diversity of our teams CRAs are provided with multiple opportunities to excel and discover where their skills can take them.
Who Were Looking For
- Detailoriented and a strong problem solver
- Highly communicative collaborative and adaptable
- Motivated accountable and able to work independently
- Positive professional and comfortable supporting virtual and inperson teams
What Youll Do
- Monitor clinical trial sites through onsite and remote visits
- Build and maintain strong relationships with investigators and site staff
- Collaborate with crossfunctional teams to meet project timelines
- Manage sitelevel study documentation systems updates and visit reports
- Implement corrective actions when needed to maintain study integrity
- Ensure sites are always audit- and inspection-ready
Additional Details
- Homebased role; only candidates residing in São Paulo City Rio de Janeiro City Curitiba or Porto Alegre are eligible
- Must be fluent in English and Portuguese
- Bachelors degree in life sciences pharmacy nursing or related field is required
- A minimum of 1 year of CRA experience required
- Must be able to travel and hold a valid drivers license
Why Join Us
- Be part of groundbreaking projects pushing the boundaries of clinical research
- Work in a collaborative and inclusive environment that values your expertise
- Unlock career growth and professional development opportunities
- Enjoy worklife balance and flexible working arrangements
If this job doesnt sound like your next step but you know someone whod be a perfect fit feel free to share this opportunity with them!
At Parexel we embrace flexibility and understand the importance of balancing your career with your personal life. Come join us where learning is constant and youre exposed to a world of experiences and open doors.
Required Experience:
Senior IC
When our values align theres no limit to what we can achieve.At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in...
When our values align theres no limit to what we can achieve.
At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us no matter what we do at Parexel contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally we do it with empathy and were committed to making a difference.
At Parexel we are a leading Clinical Research Organization (CRO) specializing in delivering lifechanging medicines to patients. We are seeking a Clinical Research Associate (CRA) to join our team. As a CRA youll be joining a fastpaced driven environment thats helping to make a lifechanging difference to patients by ensuring highquality clinical trial execution building strong site partnerships and maintaining compliance across all phases of a study. Through the collaboration and diversity of our teams CRAs are provided with multiple opportunities to excel and discover where their skills can take them.
Who Were Looking For
- Detailoriented and a strong problem solver
- Highly communicative collaborative and adaptable
- Motivated accountable and able to work independently
- Positive professional and comfortable supporting virtual and inperson teams
What Youll Do
- Monitor clinical trial sites through onsite and remote visits
- Build and maintain strong relationships with investigators and site staff
- Collaborate with crossfunctional teams to meet project timelines
- Manage sitelevel study documentation systems updates and visit reports
- Implement corrective actions when needed to maintain study integrity
- Ensure sites are always audit- and inspection-ready
Additional Details
- Homebased role; only candidates residing in São Paulo City Rio de Janeiro City Curitiba or Porto Alegre are eligible
- Must be fluent in English and Portuguese
- Bachelors degree in life sciences pharmacy nursing or related field is required
- A minimum of 1 year of CRA experience required
- Must be able to travel and hold a valid drivers license
Why Join Us
- Be part of groundbreaking projects pushing the boundaries of clinical research
- Work in a collaborative and inclusive environment that values your expertise
- Unlock career growth and professional development opportunities
- Enjoy worklife balance and flexible working arrangements
If this job doesnt sound like your next step but you know someone whod be a perfect fit feel free to share this opportunity with them!
At Parexel we embrace flexibility and understand the importance of balancing your career with your personal life. Come join us where learning is constant and youre exposed to a world of experiences and open doors.
Required Experience:
Senior IC
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