Clinical Trials Coordinator

Há 12 horas


São Paulo, São Paulo, Brasil beBeeClinical Tempo inteiro R$40.000 - R$80.000

Are you a diligent and detail-oriented individual with a strong understanding of clinical trials? Do you have excellent communication skills and the ability to work independently? We are seeking a Clinical Research Associate (CRA) to join our team.

As a CRA, you will be responsible for coordinating all aspects of the clinical monitoring and site management process. You will work closely with investigators, study coordinators, and other stakeholders to ensure the successful conduct of clinical trials. This role requires strong problem-solving skills, attention to detail, and the ability to manage competing priorities.

We are looking for someone who is passionate about delivering high-quality results and has a customer service mindset. As a CRA, you will be the main sponsor representative and provide key project updates to the team. You will also collaborate with the team to develop commitment to study timelines and objectives through regular visits with site staff in-person and remotely.

In this role, you will monitor multiple Phase I, II, III & IV clinical trial sites across different therapeutic areas. You will assist other CRAs with co-monitoring activities both remote and on-site. You will also utilize your technical skills with CTMS, eCRF, and eTMF to ensure patient safety and data integrity.

We offer a competitive salary and a range of benefits to support your well-being and work-life balance. Our benefits include various annual leave entitlements, health insurance options, retirement planning offerings, and a global employee assistance program. We are committed to providing an inclusive and accessible environment for all employees.

We encourage you to apply if you meet the minimum qualifications for this role. Please submit your application, including your resume and cover letter, to [insert contact information].



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