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São Paulo, São Paulo, Brasil beBeeClinical Tempo inteiro R$60.000 - R$90.000Job Title:Senior Clinical Research AssociateJob Description:We are seeking a skilled and experienced Senior Clinical Research Associate to join our team. As a key member of our clinical research operations, you will be responsible for conducting site visits, managing study documents, and collaborating with project teams to ensure the successful execution of...
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2 semanas atrás
As a Clinical Research Medical Advisor, you will play a pivotal role in driving high-quality clinical trials and accelerating access to innovative treatments. This position offers an exceptional opportunity to collaborate with cross-functional teams and external experts to bring impactful therapies to patients faster.
About the JobThis is an exciting opportunity for a skilled Clinical Research Medical Advisor to join our team and contribute meaningfully to global health outcomes. The successful candidate will have the ability to influence trial strategy, enhance patient engagement, and drive fast and high-quality trial site start-up through expert input during planning phases.
The ideal candidate will have a strong understanding of clinical development processes and ICH/GCP guidelines, as well as excellent communication skills in English. They should be able to lead cross-functional teams and resolve complex clinical issues, and possess a minimum of 3 years of experience in clinical development or clinical practice.
Responsibilities- Validate study designs and assess trial feasibility based on clinical practice and competitive analysis.
- Drive fast and high-quality trial site start-up through expert input during planning phases.
- Provide clinical expertise for IRB/EC interactions and informed consent content.
- Develop trial plans that address recruitment challenges and ensure data quality.
- Deliver robust training on indications, compounds, and protocols to internal and external stakeholders.
- Lead clinical recruitment strategies using physician insights and patient engagement.
- Support regulatory inspections and audits with scientific and clinical expertise.
- Ensure adherence to safety standards and provide medical input on adverse events.
- You must have an advanced scientific degree (M.D. highly preferred; Ph.D. or Pharm.D. also considered).
- You should have a strong understanding of clinical development processes and ICH/GCP guidelines.
- A minimum of 3 years of experience in clinical development or clinical practice is required.
- You must be able to lead cross-functional teams and resolve complex clinical issues.
- Excellent communication skills in English are essential.
- You should be able to deliver high-quality presentations and adapt across therapeutic areas.
- Subspecialty training or experience with Real World Evidence (RWE) is desirable.
- Familiarity with innovative study designs and data sources such as registries or electronic health records is also desirable.
