Empregos atuais relacionados a Clinical Research Associate I - Brasil - BeiGene
-
Clinical Research Associate II
1 semana atrás
Brasil Pharmaceutical Research Associates, Inc Tempo inteiroOverviewWe are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.ResponsibilitiesWhat you...
-
Clinical Research Associate II
Há 3 dias
Brasil Pharmaceutical Research Associates, Inc Tempo inteiroOverviewWe are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.ResponsibilitiesWhat you...
-
Clinical Research Associate
Há 6 dias
Brasil beBeeClinical Tempo inteiro R$35.000 - R$55.000Research Associate PositionA Research Associate plays a vital role in the success of clinical research by ensuring data integrity and patient safety.This position offers an opportunity to work with a comprehensive clinical research organization that prioritizes building a diverse culture, rewarding high performance, and nurturing talent.The ideal candidate...
-
Senior Clinical Research Associate
Há 2 dias
Brasil beBeeClinicalResearch Tempo inteiro R$170.000 - R$190.000Job Title:The role of a Senior Clinical Research Associate encompasses responsibilities across various aspects of clinical trial management.Developing strong site relationships is essential for the continuity of site interactions throughout all phases of the trial.Clinical study site management and monitoring activities must be performed in compliance with...
-
Brasil beBeeClinicalResearchAssociate Tempo inteiro R$45.000 - R$90.000Job Title: Clinical Research AssociateA key professional role in accelerating drug/device/outcomes research is that of the Clinical Research Associate (CRA). As a vital member of our team, you will play a pivotal part in ensuring patient safety and data integrity through independent monitoring of studies.The successful candidate will join a comprehensive...
-
Clinical Research Professional
Há 5 dias
Brasil beBeeClinicalResearch Tempo inteiro R$99.408 - R$141.984Job TitleWe are seeking a skilled and experienced professional to fill the role of Clinical Research Associate. The ideal candidate will have a strong background in clinical research, excellent communication skills, and the ability to work effectively in a team environment.
-
Clinical Research Associate
1 semana atrás
Brasil beBeeClinicalResearchAssociate Tempo inteiro R$90.000 - R$120.000Job Summary">A Clinical Research Associate plays a vital role in advancing drug/device/outcomes research by independently monitoring studies to ensure patient safety and data integrity. In this position, you will join a collaborative program that employs an extensive co-monitoring approach, fostering a supportive work environment.The ideal candidate will be...
-
Clinical Research Associate II
Há 7 dias
Brasil Pharmaceutical Research Associates, Inc Tempo inteiroOverviewWe are currently seeking a Clinical Research Associate to join our diverse and dynamic team at ICON Plc. As a key member of our research department, you will be responsible for overseeing and coordinating clinical trials, ensuring compliance with regulations, and collecting and analyzing critical data.ResponsibilitiesWorking independently and...
-
Clinical Research Specialist
Há 2 dias
Brasil beBeeResearch Tempo inteiro US$750.000 - US$1.150.000Clinical Research SpecialistA Clinical Research Associate is a professional who contributes to expedited drug/device/outcomes research through independent monitoring of studies to ensure patient safety and data integrity.This role offers a supportive and collaborative work environment where you will be part of an extensive co-monitoring program, enabling...
-
Clinical Research Associate II
Há 3 dias
Brasil Pharmaceutical Research Associates, Inc Tempo inteiroOverviewWe are currently seeking a Clinical Research Associate to join our diverse and dynamic team at ICON Plc. As a key member of our research department, you will be responsible for overseeing and coordinating clinical trials, ensuring compliance with regulations, and collecting and analyzing critical data.ResponsibilitiesWorking independently and...
Clinical Research Associate I
Há 1 mês
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.
General Description:
The CRA I is responsible to complete the requirements of the BeiGene CRA Training Program (12-14 weeks) prior to assignment as a primary CRA. The CRA training program consists of instructor led training sessions, independent exercises, and in-field observation visits.
After successful completion of the training program, 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:
- Complete required elements of the CRA training program and meet all outlined deadlines
The following functions may apply based on study and program requirements
- 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 per monitoring plan and applicable SOPs
- 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
- Communicate site performance to the Clinical Study Team (CST)
- May serve as mentor/trainer for less experienced CRAs to assist with general and study-specific monitoring issues
- Perform study-specific training with project team
- Perform Serious Adverse Event (SAE) reconciliation and work with study sites and CST 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 the role, as required
Minimum Requirements – Education and Experience:
BS/BA in a relevant scientific discipline. Experience working in oncology global trials and 5+ years of relevant Clinical Operations experience or 1+ years in a clinical research associate position is preferred.
Other Experience:
- 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 assigned study sites
- Co-monitoring with CRAs and support site visits, as needed
- May serve as a mentor CRA for CRAs in training
Travel: Up to 70% Travel
Computer Skills:
- Proficient in Microsoft Word, Excel, PowerPoint and Outlook
- Familiar with industry software such as CTMS, investigational product and data management
#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.
This offer from "BeiGene" has been enriched by Jobgether.com and got a 78% flex score.
