Senior Regional Clinical Trial Management Associate
Há 1 mês
BeiGene 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
Language Requirement : Fluent English and Portuguese. Spanish is a plus.
Preferred Experience : Pharmaceutical/Biotech Industry, Hematology, Oncology
General Description:
Please note: this is a Hybrid position with an average of 2 days in the Sao Paulo office weekly.
Supports the Regional Clinical Study Manager in regional study delivery and ensures that delegated components of clinical studies are executed to expected and specified quality standards, within timelines and budget. Supports the Clinical Research Associates and/or Study Start-up Specialists in country study delivery and ensures that delegated components of clinical studies are executed per expected and specified quality standards. Applies knowledge of clinical trials operations in the region under guidance of the Regional Clinical Study Manager. Supports the alignment of regional deliverables with overall study goals under the direction of the Regional Clinical Study Manager. Supports regional vendor management in addition to other regional study management activities. Participates internal working groups, initiatives. Provides knowledge and expertise in a specific process as a subject matter expert (SME). Might mentor other team members. Performs other tasks assigned by the line manager.Essential Functions:
Regional Trial Support & Collaboration
Acquires regional study management experience by supporting to oversee multiple aspects of clinical trial conduct including feasibility assessment, study start-up, document generation and review, tracking of samples and enrollment of study participants. Acquires country study management experience by supporting CRAs and/or SSUSs with multiple aspects of clinical trial conduct including CTMS updates, ISF binder preparation, document collections, ICF customization, eTMF maintenance (document filing, reconciliation and review at site level or country level. Knowledgeable of clinical research operations, including interpretation and implementation of regulations/ICH guidelines. Supports the Regional Clinical Study Manager with set up and logistics of regional team meetings (agenda, minutes, etc.). Supports the Country Heads with set up and logistics of regional team meetings (agenda, minutes etc.). Establishes good collaboration with key stakeholders regionally, globally and at country level (Regional Clinical Study Manager, Regional Clinical Trial Management Associate, Global Study Management Associate, Clinical Research Associates and Study Start-up Specialists). As required, supports CRAs with various activities such as monitoring visit preparations, equipment management, Contract support, EC/regulatory submission preparation/tracking, TMF filing, SUSAR submission, etc.Timelines, Planning and Execution
Creates and maintains regional/country level SharePoint folders for the study and regional study team distribution lists. Sets up the countries and sites in the region in the appropriate systems e.g., eTMF, CTMS, etc. and makes sure information is kept up to date. Supports system access requests for the region/country and ensure these are managed appropriately across the study life cycle, supports user account management for users in region. Might support the local adaptation of global documents under supervision of the Regional Clinical Study Manager. May assist in the review of study-related documents as they relate to the supported clinical trials as delegated by the Regional Clinical Study Manager (e.g., Informed consent forms, regional Pharmacy Manual, Laboratory Manual, Patient Diary, Clinical Site Procedures Manual, Pharmacy Manual, CRF Completion Guidelines and other relevant regional study plans and charters). Supports study start up in region/country in close collaboration with the regional study start up team and the Regional Clinical Study Manager. Supports the organization of study specific investigator meetings together with the Regional Clinical Study Manager and the Global Study Management Associate. Supports the TMF specialist with country/site level TMF creation and maintains the country/site level TMF including regular review and QC of TMF documents as per the study TMF QC plan. Helps resolving any regional/country specific issues related to clinical supplies in collaboration with relevant stakeholders. Supports the data cleaning activities and contributes to the follow up of outstanding information for region/country. Prepares site newsletters and other correspondence related to clinical trial conduct (e.g., best practices and lessons learned, frequently asked questions) in collaboration with the study team. Might assist in resolution of routine study questions from clinical trial sites. Might support the maintenance of information for region/country in relevant public registries (e.g., CT.gov). Supports the Regional Clinical Study Manager with providing all relevant information from region/country to be included in the Clinical Study Report.Quality
Supports the identification of operational risks and works with the Regional Clinical Study Manager to recommend solutions for discussion with appropriate team leadership. Learns and shares best practices in clinical operations methodologies, systems, and processes with the emphasis on quality and compliance. Might support the preparation of sites for quality assurance audits and inspections. Suggests improvements to enhance the efficiency and the quality of the work performed on assigned projects. Supports the development of local/regional tools, working instructions and SOPs.Budget
Supports selection and set up of vendors for activities outsourced in region/country. Supports management of regional study budget incl PO set up. Supports management of regional vendors incl PO set up. Supports with payments follow up (sites, stakeholders). Might assist accrual activities, if required.Minimum Requirements – Education and Experience:
Preferably Bachelor’s Degree, preferably in a scientific or healthcare discipline required. Higher Degree preferred. Exceptions might be made for candidates with relevant clinical operations experience. 2 or more years of experience in clinical research within biotech, pharma or CRO industryOther Qualifications:
Knowledge of clinical operations methodologies, understanding of operational aspects of clinical study processesSupervisory Responsibilities: Might mentor other team members.
Travel: Limited travel might be required
Computer Skills: MS Office, eTMF, CTMS
#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-
Senior Regional Clinical Trial Management Associate
2 meses atrás
São Paulo, SP, Brasil BeiGene Tempo inteiroPLEASE SUBMIT ALL RESUMES/CV'S IN ENGLISH FOR CONSIDERATION Language Requirement: Fluent English and Portuguese. Spanish is a plus. Preferred Experience: Pharmaceutical/Biotech Industry, Hematology, Oncology General Description: - Supports the Regional Clinical Study Manager in regional study delivery and ensures that delegated components of clinical...
-
Clinical Trial Management Associate Manager
6 meses atrás
Sao Paulo, Brasil BeiGene Tempo inteiroPLEASE SUBMIT ALL RESUMES/CV'S IN ENGLISH FOR CONSIDERATION Language Requirement: Fluent English and Portuguese. Spanish is a plus. Preferred Experience: Pharmaceutical/Biotech Industry, Hematology, Oncology Company Overview: BeiGene, Ltd. (NASDAQ: BGNE; HKEX: 06160) is a global, commercial-stage, research-based biotechnology company focused on...
-
(Senior) Clinical Trial Manager
6 meses atrás
São Paulo, Brasil IQVIA Tempo inteiroClinical Trial Manager – Sponsor Dedicated. Clinical Trial Manager provides for the regional/global coordination of clinical trial management activities for internally managed and/or outsourced trials. These services lead the Study Management Team (SMT) and ensure regional/global clinical operations deliverables progress according to agree upon...
-
São Paulo, São Paulo, Brasil Parexel International Tempo inteiroAbout the RoleWe are seeking an experienced Clinical Research Associate II to conduct onsite monitoring visits in Brazil. This role offers the opportunity to build and maintain site relationships, ensuring they're set up for success.Key ResponsibilitiesLeverage your expertise to conduct qualification visits, site initiation visits, monitoring visits, and...
-
São Paulo, São Paulo, Brasil BeiGene, Ltd. Tempo inteiroEstimated Salary: $80,000 - $110,000 per annumIn this challenging and rewarding role, you will support the Regional Clinical Study Manager in delivering clinical studies across the region. As a key member of the team, you will be responsible for ensuring that delegated components of clinical studies are executed to expected quality standards, within...
-
Clinical Trials Assistant 1
7 meses atrás
Sao Paulo, Brasil IQVIA Tempo inteiroJob Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...
-
Principal Clinical Research Associate
6 meses atrás
Sao Paulo, Brasil CTI Clinical Trial Services, Inc Tempo inteiro**Principal Clinical Research Associate** **Please submit your CV in English for Quickest Review Process!** Maintaining our company culture across all regions, and especially with our remote employees, is incredibly important to our overall success. To do so, we have weekly all-staff meetings in which each department can provide an update on a study or...
-
Clinical Trials Assistant 1
7 meses atrás
Sao Paulo, Brasil Novasyte Tempo inteiroJob Overview Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. Essential Functions - Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical...
-
Principal Clinical Research Associate
2 meses atrás
São Paulo, Brasil CTI Clinical Trial Services, Inc Tempo inteiroPrincipal Clinical Research AssociatePlease submit your CV in English for Quickest Review Process! Maintaining our company culture across all regions, and especially with our remote employees, is incredibly important to our overall success. To do so, we have weekly all-staff meetings in which each department can provide an update on a study or milestone that...
-
Clinical Trials Operations Lead
Há 2 dias
São Paulo, São Paulo, Brasil Icon Plc Tempo inteiroAt Icon Plc, we're dedicated to advancing clinical research and improving patient outcomes. As a Clinical Trial Manager in our Real World Solutions team, you'll play a critical role in delivering high-quality clinical trials.**Job Summary:**We're seeking an experienced Clinical Trial Manager to oversee the operational aspects of our clinical trials. In this...
-
Clinical Trial Manager
6 meses atrás
Sao Paulo, Brasil ICON plc Tempo inteiroJob Advert Posting ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to...
-
Contract Clinical Trial Senior Analyst
6 meses atrás
Sao Paulo, Brasil Johnson & Johnson Tempo inteiroDiversity, Equity & Inclusion are essential to continue building our history of pioneering and innovation, which has been impacting the health of more than 1 billion patients and consumers every day for more than 130 years. Regardless of your race, belief, sexual orientation, religion, or any other trait, YOU are welcome in all open positions at the largest...
-
Regional Clinical Trial Operations Specialist
4 semanas atrás
São Paulo, São Paulo, Brasil Beigene Tempo inteiroAbout BeiGeneBeiGene continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals in the biotech industry.Salary Information:The estimated salary range for this position is $80,000 - $110,000 per year, depending on experience.Job DescriptionWe are seeking a skilled Regional Clinical Trial Operations Specialist...
-
Clinical Trial Project Manager
1 semana atrás
São Paulo, Brasil Medpace Tempo inteiroJob SummaryMedpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers / Project Managers to join our Clinical Trial Management Group in Sao Paulo, Brazil . Our therapeutic areas of focus include Oncology, Cardiovascular/Metabolic, Infectious Disease, CNS and more. We provide remote flexibility with relevant...
-
Clinical Trial Project Manager
Há 2 horas
São Paulo, Brasil buscojobs Brasil Tempo inteiroMedpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers / Project Managers to join our Clinical Trial Management Group in Sao Paulo, Brazil . Our therapeutic areas of focus include Oncology, Cardiovascular/Metabolic, Infectious Disease, CNS and more. We provide remote flexibility with relevant experience....
-
Sr Clinical Trial Management, Vaccines
6 meses atrás
Sao Paulo, Brasil Thermo Fisher Scientific Tempo inteiroAt Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through...
-
São Paulo, São Paulo, Brasil ICON Plc Tempo inteiroOverview of ICON PlcICON Plc is a leading healthcare intelligence and clinical research organization dedicated to shaping the future of clinical development.Salary InformationWe are offering a competitive annual salary of approximately $110,000 - $140,000 based on experience.Job ResponsibilitiesAs a Senior Clinical Trial Manager at ICON Plc, you will be...
-
Clinical Trial Project Manager
1 semana atrás
São Paulo, Brasil Medpace Tempo inteiroJob Summary Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers / Project Managers to join our Clinical Trial Management Group in Sao Paulo, Brazil . Our therapeutic areas of focus include Oncology, Cardiovascular/Metabolic, Infectious Disease, CNS and more. We provide remote flexibility with...
-
Research Project Coordinator
Há 1 mês
São Paulo, São Paulo, Brasil Bancroft School Tempo inteiroJob SummaryWe are seeking a highly skilled Clinical Research Project Coordinator to join our team in clinical trial management. As a key member of our team, you will be responsible for coordinating projects from start to finish, ensuring timely delivery and high accuracy.About the RoleThe successful candidate will have a Bachelor's degree in a health...
-
Clinical Trial Project Manager
Há 5 dias
São Paulo, Brasil Medpace Tempo inteiroJob SummaryMedpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers / Project Managers to join our Clinical Trial Management Group in Sao Paulo, Brazil . Our therapeutic areas of focus include Oncology, Cardiovascular/Metabolic, Infectious Disease, CNS and more. We provide remote flexibility with relevant...
