Clinical Research Associate Ii - Sao Paulo, Brasil - BeiGene

BeiGene

Empresa verificada

Sao Paulo, Brasil

há 3 semanas

Postado por:

Ana Silva

beBee Recruiter

Descrição

PLEASE SUBMIT ALL RESUMES/CV'

S IN ENGLISH FOR CONSIDERATION

PREFERRED EXPERIENCE:
Pharmaceutical/Biotech Industry, Hematology, Oncology

PREFERRED:
Combination of Portuguese, Spanish and English Speaking

PLEASE NOTE:
This is a Hybrid Position based in Sao Paulo times per week in Office)

Company Overview:
BeiGene, Ltd

(NASDAQ:

BGNE;

HKEX:
is a global, commercial-stage, research-based biotechnology company focused on molecularly targeted and immuno-oncology cancer therapeutics.

With a team of over 10,000 employees across China, the United States (Cambridge, MA; Ridgefield Park, NJ; Emeryville, CA & San Mateo, CA), Switzerland, Australia and Brazil, BeiGene is advancing a pipeline consisting of novel oral small molecules and monoclonal antibodies for the treatment of cancer.

BeiGene is working to create combination solutions aimed at having both a meaningful and lasting impact on cancer patients

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 studyspecific monitoring issues
Communicate site performance to the Clinical Study Team (CST)
Perform studyspecific 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 2+ years of relevant Clinical Operations experience, and minimum of 1+ years of monitoring

experience. Experience in global oncology trials preferred.

Other Qualifications:

Pharmaceutical or Biotech experience preferred
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 multitask
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
Comonitoring 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

BeiGene Global Competencies

When we exhibit our values of Patients First, Collaborative Spirit, Bold Ingenuity and Driving Excellence, 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 and we value diversity.

BeiGene 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.