Current jobs related to Clinical Research Associate II - Greater Toronto and Hamilton Area - Nexcella, Inc.
-
Clinical Research Associate II
1 week ago
Greater Toronto Area, Canada ICON Strategic Solutions Full timeICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical developmentJob Advert PostingAs a CRA you will be joining the world's largest & most comprehensive clinical...
-
Clinical Research Coordinator Ii
2 weeks ago
Toronto, Canada Centricity Research Full time**Clinical Research Coordinator II (CRC II)** **Join Us at Centricity Research!** Centricity Research is one of the largest clinical research networks in North America. We are a fully centralized Integrated Research Organization (IRO) specializing in conducting Phase I-IV clinical trials in over 35 therapeutic areas: inpatient and outpatient;...
-
Clinical Research Coordinator
4 days ago
Toronto, Canada Clinical Research Full timeResponsibilities: - Coordinate and oversee clinical research studies from start to finish - Collect and record data accurately and efficiently - Analyze research data and prepare reports for review - Ensure compliance with study protocols, regulations, and ethical guidelines - Collaborate with healthcare professionals, researchers, and study participants -...
-
Clinical Research Coordinator
2 weeks ago
Hamilton, Canada LEADER research Full time**Clinical Research Coordinator - Job Posting** **LEADER Research - Hamilton/ON** **Full Time** 37.5 hours per week/ Day shifts Mid/Senior Level LEADER Research is a research site with specialized focuses on clinical immunological and dermatological diseases. Our centre conducts and coordinates phase II-IV clinical trials to contribute to the...
-
Clinical Research Associate Ii
2 weeks ago
Toronto, Canada Sunnybrook Health Sciences Centre Full time**Clinical Research Associate II; Sunnybrook Research Institute, Odette Cancer Centre Clinical Trials** **Regular Full-time** **Sunnybrook Research Institute** **Fully Affiliated with the University of Toronto** **Vacancy Exists For: Clinical Research Associate II** **Summary of Duties and Responsibilities**: The Odette Cancer Center (OCC) Clinical...
-
Clinical Research Associate Ii
5 days ago
Toronto, Canada Fortrea - Organic Full timeClinical Research Associate II Remote - Canada Phase IV Registries - Rare Disease As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and...
-
Clinical Research Coordinator Ii
6 days ago
Toronto, Canada Syneos - Clinical and Corporate - Prod Full time**Description** Clinical Research Coordinator II Illingworth Research Group provides a range of patient focused clinical services to the pharmaceutical, healthcare, biotechnology and medical device industries. These include mobile research nursing, patient concierge, medical photography and clinical research services. Illingworth are experts with...
-
Clinical Research Associate
4 weeks ago
Toronto, Canada Translational Research in Oncology Full timeIf you are an experienced CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you! Translational Research in Oncology (TRIO) is a global clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is...
-
Clinical Research Associate
4 weeks ago
Toronto, Canada Translational Research in Oncology Full timeIf you are an experienced CRA who is passionate about oncology research and looking to join a highly skilled and knowledgeable team, TRIO is the place for you! Translational Research in Oncology (TRIO) is a global clinical research organization dedicated to advancing translational cancer research in the clinical trial setting. Our passionate team is...
-
Clinical Research Associate II
4 weeks ago
Toronto, ON, Canada Nexcella, Inc. Full timeClinical Research Associate II (Cell Therapy) Greater Toronto Area / Hybrid Greater Montreal Area / Hybrid Our 3 Core Values • Intelligence • Integrity • Initiative Our mission is to harness the immune system through innovative cell therapies and other modalities to deliver widely accessible cures. Patients are waiting! What You'll Do The Clinical...
Clinical Research Associate II
4 weeks ago
Clinical Research Associate II (Cell Therapy) Greater Toronto Area / Hybrid Greater Montreal Area / Hybrid Our 3 Core Values • Intelligence • Integrity • Initiative Our mission is to harness the immune system through innovative cell therapies and other modalities to deliver widely accessible cures. Patients are waiting What You'll Do The Clinical Research Associate (CRA) II will be the primary liaison between the Investigator sites and Nexcella, responsible for overall site conduct and establishing important relationships with key site personnel. The CRA will perform key job functions in accordance with ICH Good Clinical Practice (ICH GCP), FDA regulations, Nexcella SOPs and work practices while supporting the organizational mission to advance the development of promising oncology therapies and technologies to benefit patients. CRAs are expected to work in a hands-on, highly visible and autonomous role. CRAs must have the ability to be flexible and represent Nexcella in a positive and professional manner while collaborating across all levels with the clinical teams and Sponsors/vendors. Responsibilities : • Perform site selection, initiation, monitoring, and close-out visits of investigational sites for the Nexcella portfolio of clinical trials. • Manage the progress of assigned sites by tracking patient recruitment and enrollment, CRF completion and submission, source data verification, data collection, and data query generation and resolution. • Conduct monitoring activities, including, but not limited to the following: o Ensuring PI oversight of all trial activities o Source data review and verification with EDC fields o Essential documentation review and reconciliation o Investigational Product (IP) management and accountability o Lab/kit supply management • Develop collaborative relationships with investigative sites and personnel. • Maintain communication with sites through frequent contact to ensure site compliance, adequate enrollment, and understanding of study requirements. • Write and submit complete and accurate visit letters and reports of investigational site findings and update applicable CTMS. • Escalates observed deficiencies, issues, and corrective and preventative action plans as appropriate. • Participate in audit preparations and follow-up, as needed. • Review and address protocol deviations, data quality issues, and identify process improvements for assigned sites. • Be a collaborative member of the study team: provide insight, updates, and strategies to improve processes. • Ability to think critically while prioritizing tasks in an efficient manner to meet study deliverables. • Contribute to CRF development and perform User Access Testing, as requested. • Assist with other duties as assigned. Qualifications: • Bachelor’s degree in life science/biomedical/medical science with a proficient knowledge of the clinical/scientific terminology and methods common to the oncology therapeutic setting. • 2+ years clinical research experience is required. • 2+ years experience at a CRO or Sponsor required. • Independent field monitoring experience of oncology clinical trials is required. • Early phase oncology experience is preferred. • Proficient knowledge and practical utilization of ICH- GCP and applicable regulatory requirements. • Strong communication (written and verbal) and interpersonal skills. • Demonstrate effective presentation skills by clearly explaining complex concepts to a broad range of audiences. • Ability to independently prioritize tasks with excellent time management skills. • Highly proficient in computer applications including Microsoft suite of applications, EDC and CTMS applications. • Fluent in English (written and verbal) About Nexcella Nexcella Inc., a wholly-owned Immix Biopharma subsidiary, is a clinical-stage biopharmaceutical company trailblazing cell therapies in AL Amyloidosis and other serious diseases. Our lead candidate is sterically-optimized BCMA-targeted chimeric antigen receptor T (CAR-T) cell therapy NXC-201. Learn more at
