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Clinical Trial Management Associate Jobs

Clinical Trial Associate (Cta) - Remote, Us
By ICON Strategic Solutions At United States
Management/reconciliation, and accruals in support of the CTM and Finance.
Responsible for data entry into Clinical Trial Management Systems.
management/reconciliation, and accruals in support of the CTM and Finance.
Supports and/or tracks external access rights to Clinical Trial Management Systems.
Manage and track clinical and non-clinical supplies.
Bachelor’s degree or equivalent undergraduate degree with science or healthcare experience preferred
Sr. Clinical Trial Associate
By Omeros Corporation At , $75,000 - $90,000 a year
Experience and knowledge of ICH GCP and eTMF management
Education, Experience, Knowledge, & Skills Required:
Assists with site management at the direction of other clinical personnel
Assists with the management and tracking of study projects using the CTMS or other electronic means
Previous CTA experience working with CROs and vendors
Demonstrated experience working effectively in a fast-paced team environment
Associate Clinical Trial Transparency Associate
By ICON At , Remote
Experience in the use of Doc base system or similar Electronic Document Management system is a plus
Participates in user acceptance testing (UAT) testing, document/data management/clean-up projects, audit preparation and participation when applicable
Experience or general understanding of the European Medicines Agency's (EMA) and/or Health Canada publication of clinical information requirements.
Experience or general understanding of US and EU clinical trial disclosure requirements
Demonstrated good judgment and independent decision-making abilities, as well as strong follow-up skills
Supports trial transparency processes. Responsibilities may include any of the following:
Clinical Trial Associate Jobs
By Catalyst Clinical Research At Raleigh, NC, United States
Participate in or manage non-study related projects or initiatives.
Manage and oversee process implementation and collect feedback.
Excellent written and verbal capabilities that facilitate internal and external communications.
Employee may be office or remote based.
Participates in the hand over meeting from feasibility team member.
Maintenance and coordination of the logistical aspects of clinical trials according to GCP and ICH relevant SOP’s.
Bilingual Associate Clinical Trial Manager
By Novocure At , Portsmouth, 03801
Global trial management experience preferred
Supports the development and management of the project timeline, forecasting and tracking milestones
Performs risk management, including identifying, tracking, and evaluating potential risks and mitigation strategies; maintains risk log and implements risk responses
Collaborates internally to oversee clinical supplies and device management
Supports protocol deviation management, including tracking and routine review
Oversees clinical monitoring and site management; reviews monitoring visit reports and conducts co-monitoring visits
Clinical Trial Transparency Associate
By ICON plc At ,

The Clinical Data Disclosure & Transparency (CDD&T) Disclosure Specialist will support the client’s clinical trial transparency processes in compliance with trial transparency laws and ...

Clinical Trial Associate Jobs
By ICON Strategic Solutions At Palo Alto, CA, United States
Support clinical trial registration and disclosure on websites per applicable regulatory requirements
At least 1 year experience as a CTA, CRC, or other role in clinical trials.
Proven organizational and presentation skills
Ability to manage multiple tasks with meticulous attention to detail
Excellent written and verbal communication skills
Good knowledge of the ICH/GCP
Clinical Trial Associate Jobs
By DynamiCure Biotechnology At Massachusetts, United States
Other projects/duties as assigned for the overall benefit of the organization Required Education, Experience, Skills, and Competencies
Liaise with Clinical Sample Management for the tracking and coordination of biomarker testing with 3rd party labs
At least 2 years of experience in a clinical research environment
Willingness to learn, able to take direction and ability to manage multiple tasks
Outstanding organizational, critical thinking, and problem-solving skills
Excellent written and verbal and communication skills
Clinical Trial Associate Jobs
By Collabera At North Chicago, IL, United States
Identifies conflicts and resolves or elevates them to management to ensure resolution.
2 years of writing experience preferred
Completes activities to assist in ensuring timely disclosure of accurate, consistent, aligned and complete information globally.
Communicates deliverables, process and timelines effectively across functional areas and within department to accomplish project objectives.
Coordinates the review, approval, and other appropriate functions.
Exhibits a moderate level of technical competencies and requires a low level of counsel and guidance.
Clinical Trial Associate Jobs
By Randstad Life Sciences US At Raleigh-Durham-Chapel Hill Area, United States
Identifies conflicts and resolves or elevates them to management to ensure resolution.
Responsibilities will be focused on supporting EU CTR applications and documentation.
2 years of writing experience preferred
Familiarity with clinical study and site start up documentation is preferred.
Completes activities to assist in ensuring timely disclosure of accurate, consistent, aligned and complete information globally.
Communicates deliverables, process and timelines effectively across functional areas and within department to accomplish project objectives.
Clinical Trial Disclosure Associate
By Randstad USA At North Chicago, IL, United States
Identifies conflicts and resolves or elevates them to management to ensure resolution.
2 years of writing experience preferred
Completes activities to assist in ensuring timely disclosure of accurate, consistent, aligned and complete information globally.
Communicates deliverables, process and timelines effectively across functional areas and within department to accomplish project objectives.
Coordinates the review, approval, and other appropriate functions.
Exhibits a moderate level of technical competencies and requires a low level of counsel and guidance.
Clinical Trial Disclosure Associate (Clinical Trial Registries)
By Rangam At United States
Identifies conflicts and resolves or elevates them to management to ensure resolution.
Responsibilities will vary based upon business need.
2 years of writing experience preferred
Candidates can be remote, located anywhere in the US.
Completes activities to assist in ensuring timely disclosure of accurate, consistent, aligned and complete information globally.
Communicates deliverables, process and timelines effectively across functional areas and within department to accomplish project objectives.
Clinical Trial Associate - Oncology
By BioSpace At New York, NY, United States
Knowledge of clinical trial regulations, guidelines, and best practices, including ICH-GCP and FDA requirements
Strong organizational skills and attention to detail, with the ability to manage multiple tasks and prioritize workload effectively
Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems
Excellent written and verbal communication skills, with the ability to effectively interact with study team members and internal / external stakeholders
Mental health and wellness benefits
Support the organization and conduct of investigator meetings, study initiation visits, and other trial-related meetings
Project Manager – Clinical Trial Management Systems
By OSI Engineering At Oakland, CA, United States
Previous clinical trials experience in a similar role providing project management, solutions management, and IT solutions to a clinical trials program.
IT project management experience related to implementing and optimizing components in clinical trial digital ecosystems.
5+ years of experience in system design/ architecture project manager/ related position.
Provide support and manage areas of System Design/ Architecture.
Experience working with Tableau or similar analytic reporting software.
Experience working on any kind of benchmarking and/ or milestone reporting software to show metrics and progress.
Sr. Clinical Trial Associate
By Randstad USA At New Jersey, United States
Update the clinical trial management system (CTMS) for assigned trials with updates working with the trial manager.
Manage internal study meetings inclusive of setting agendas, recording and distributing minutes.
4+ years of clinical trial experience, with 2+ years of industry experience supporting clinical studies at a CRO or pharmaceutical company
1+ years of experience working directly for a sponsor is also preferred
Excellent written and verbal communication skills.
Support the clinical operations team with all aspects from study start-up, maintenance and close-out.
Clinical Trial Associate Jobs
By Skills Alliance At United States
• Excellent communication, time management and organizational skills
• Work with the clinical operations team to prepare metrics and updates for management
• 2+ years of experience in a clinical operations role in the biopharmaceutical industry
• Experience planning and tracking deliverables and timelines
• Take ownership of assigned responsibilities, with guidance
• Specific experience in Lymphoma or CAR T trials
Clinical Trial Associate (Contract)
By Clora At United States

Location: Remote w/ US travel

Vice President Clinical Trial Management
By Apsida Life Science At United States
Experience in successfully leading global CRO Project Management or Clinical Trial Management teams.
Previous experience and proven ability to lead staff, think strategically, and execute organizational strategy.
Masters or PhD in life sciences/medical field;
Clinical Trial Associate/Coordinator
By EG Life Sciences At United States
Liaise with Clinical Sample Management for the tracking and coordination of biomarker testing with 3rd party labs
Infectious Disease, Vaccines, CRO Management, Unblinded
3+ years of Clinical Research Experience:
ADDITIONAL QUALIFICATIONS / NICE TO HAVES
Maintain clinical trial files (including eTMF), project processes, tracking systems, and other utilized study or departmental systems
Coordinate Project Team and departmental meetings, including associated documentation
Associate Clinical Trial Leader / Clinical Trial Leader - Dual Posting
By Novartis At East Hanover, NJ, United States
Support the implementation of best practices and standards for trial management, including sharing lessons learned.
Contribute to the implementation of best practices and standards for trial management, including sharing lessons learned.
4+ years technical, operational, managerial experience planning, executing, reporting & publishing clinical studies in pharmaceutical company or contract research organization
Basic knowledge of Good Clinical Practice and scientific principles
Advanced degree or equivalent education/degree in life science/healthcare
Knowledge of Good Clinical Practice, clinical trial design, statistics, regulatory processes & global clinical development process