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Clinical Trial Management Associate Jobs in Union, Arkansas

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
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 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
Clinical Trial Supply Associate
By Mindlance At United States
· SAP software based computer systems experience.
· MS Office and MS Teams experience.
·SKYPE Meeting or Virtual Meeting software experience.
·GMP and Pharmaceutical Industry Regulations knowledge.
Job Title:Clinical Trial Supply Chain Specialist
·Additional services provided include Product Complaint evaluation, classification, and notification, temperature excursion evaluation and processing.
Clinical Trial Associate Jobs
By NuWest Group 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 Supply Associate, Budget Management
By Watton Hall At United States
Working with vendors and vendor managers to ensure efficient collection of requirements for clinical supply chain functions.
Develop budget overviews based off vendor management, clinical systems and logistics team inputs.
Relevant degree or equivalent education within business or finance area.
Ideally experience working within pharmaceutical or biotech environment, or alternatively working within a supplier or procurement group.
Experience within budgeting and invoice tracking.
Some knowledge of supply chain processes would be advantageous.
Clinical Trial Document Management (Ctdm) Specialist
By Alcon At United States
Enter and maintain site information and document tracking in current clinical trial management systems.
Travel Requirements: minimal to no travel if located in Fort Worth; less than 10% if remote
Bachelor’s Degree or Equivalent years of directly related experience (or high school +8 yrs; Assoc.+4 yrs)
Basic knowledge of clinical trial processes
Alcon provides a robust benefits package including health, life, retirement, flexible time off, and much more!
Benefit from working in a highly collaborative and diverse environment, as well as within a welcoming and empowered team.
Clinical Trial Coordinator/Associate
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
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
Senior Clinical Trial Associate
By Translational Drug Development (TD2) At United States
Minimum of four years of experience in an administrative role.
At least four years of experience in support of clinical research with preference to oncology research.
Advanced written and verbal communication skills
Knowledge of GCP, ICH guidelines and clinical trial regulations
Experience managing Trial Master Files and/or Investigative Site Files.
Draft project plans and create project documents for review prior to Sponsor review, as assigned.
Global Clinical Trial Associate
By ICON Strategic Solutions At United States
Benefits of Working in ICON:
Organizes Study Team meetings and prepares meeting minutes
Assists with organizing Investigator Meetings
Assists with preparation and review of study documents
Ships study documents and supplies to investigational sites and tracks delivery
Submits study documentation to Trial Master File
Clinical Trial Associate - Remote
By Atlas Search At United States
Support Clinical Project Management team in communication to CRO, Vendors and Investigator Sites.
Assist Clinical Project Management team in the collection, review and filing of site Essential Documents, and maintenance of the TMF.
Minimum of 2+ years of industry experience
Participate in regular team meeting / teleconferences; CRO, Vendor and Investigator Site meetings as necessary; and Investigator Meetings, as necessary.
Bachelor’s Degree in health science or related field
Ability to travel as required.
Intern, Clinical Trial Associate
By Viatris At United States
Upload documents into electronic document management system (Documentum, D2/eTMF).
Knowledge of ICH E6 Good Clinical Practices (GCP) and clinical trial research preferred but not required.
Must possess excellent computer skills to include MS Office specifically (MS Word and MS Excel) and Adobe.
Access – Providing high quality trusted medicines regardless of geography or circumstance;
Leadership – Advancing sustainable operations and innovative solutions to improve patient health; and
Partnership – Leveraging our collective expertise to connect people to products and services.
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 ...