Clinical Research Associate III

BeiGene; São Paulo; Presencial; USD 35.000 - 50.000; Tempo integral

Resumo da oferta

A leading company in the biotech field seeks a Clinical Research Associate (CRA) in São Paulo. The role involves conducting site visits, ensuring compliance with guidelines, and building relationships within clinical study sites. Candidates should possess a relevant degree and strong experience in Clinical Operations, with the ability to travel up to 70%. Fluency in English is essential, and familiarity with oncology trials is preferred.

Serviços

Flexible working environment

Qualificações

• Minimum 3 years of relevant Clinical Operations experience.
• At least 2 years of monitoring experience.
• Experience in global oncology trials is preferred.

Responsabilidades

• Conduct site visits and monitor data quality and patient safety.
• Build relationships with key site personnel.
• Ensure compliance with ICH-GCP guidelines and regulations.

Conhecimentos

Excellent communication

Interpersonal skills

Organizational skills

Analytical Thinking/Data Analysis

Fluency in English

Formação académica

BS/BA in a relevant scientific discipline

Ferramentas

Microsoft Word

Microsoft Excel

Microsoft PowerPoint

Outlook

CTMS

Descrição da oferta de emprego

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.

PLEASE SUBMIT ALL RESUMES/CV'S IN ENGLISH FOR CONSIDERATION

Location : Sao Paulo Hybrid

Language Requirement : Portuguese and English Required and Spanish highly preferred

Required Experience : Pharmaceutical/Biotech Industry, Hematology, Oncology

General Description:

The CRA will assume the role of a primary CRA. The CRA will conduct site visits (i.e., PSSV, SIV, IMV, COV) and function as the site manager. The CRA is responsible to build and maintain relationships with key site personnel and ensure an effective line of communication. The CRA will also monitor data quality and patient safety through monitoring and site education. CRAs are to complete all aspects of the clinical monitoring process in accordance with ICH-GCP guidelines, local regulations, and applicable SOPs.

Essential Functions:

• Perform and coordinate assigned aspects of the clinical monitoring process in accordance with GCPs and SOPs to assess the safety and efficacy of investigational products and/or medical devices
• Conduct site visits to determine protocol and regulatory compliance, and prepare required documentation
• Develop collaborative relationships with investigative sites, and study vendors
• Provide protocol and related study training to assigned clinical study sites
• Attend disease indication and/or project specific training, as required
• Maintain oversight of site performance by tracking metrics for enrollment, data entry into Case Report Forms (CRFs), protocol deviation trends, and overall site issues
• Serve as mentor/trainer for less experienced CRAs to assist with general and study-specific monitoring issues
• Communicate site performance to the Clinical Study Team (CST)
• Perform study-specific training with project team
• Perform Serious Adverse Event (SAE) reconciliation and work with study sites to resolve discrepancies
• Collaborates with CST and clinical study sites to ensure timely delivery of study milestones (i.e., study startup, recruitment, database analyses, closeout, etc.).
• Attend regional investigator meeting and site booster visits, as required
• Provide audit/inspection preparation support to clinical study sites and ensure quality issues or findings are followed to resolution, as needed
• Assist with other assigned clinical responsibilities within scope of role, as required

Minimum Requirements – Education and Experience:

BS/BA in a relevant scientific discipline and minimum of 3+ years of relevant Clinical Operations experience, and minimum of 2+ years of monitoring

experience. Experience in global oncology trials preferred.

Other Experience:

• Understands clinical trial processes with a thorough knowledge of ICH and associated regulatory guidelines
• Excellent communication and interpersonal skills
• Excellent organizational skills and ability to prioritize and multi-task
• Fluent in English (writing and speaking)

Supervisory Responsibilities:

• Provides site level management for established protocols and portfolio under general supervision
• Provides mentoring/support to CRAs for CRA related topics
• Co-monitoring with CRAs and support site visits, as needed

Travel : Up to 70% travel

Computer Skills:

• Efficient in Microsoft Word, Excel, PowerPoint and Outlook
• Familiar with industry CTMS and data management systems

#LI-Remote

Global Competencies

When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity, and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.

• Fosters Teamwork
• Provides and Solicits Honest and Actionable Feedback
• Self-Awareness
• Acts Inclusively
• Demonstrates Initiative
• Entrepreneurial Mindset
• Continuous Learning
• Embraces Change
• Results-Oriented
• Analytical Thinking/Data Analysis
• Financial Excellence
• Communicates with Clarity

We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need.