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Clinical Trials Management Associate Jobs

Clinical Trials Associate - Neuroscience
By Worldwide Clinical Trials At United States
Degree level qualification or equivalent experience plus a minimum of one years’ experience in a related role
Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.)
Strong organizational and problem-solving skills
Excellent skills in MS Office applications including Outlook, Word, Excel and PowerPoint
Skill sets and proven performance equivalent to the
Maintain and quality audit to assure the most recent revisions of documents are on project portals
Research Associate Ii / Lvn, San Diego Clinical Trials (Durational W/Benefits)
By Kaiser Permanente At , San Diego $63,500 - $82,060 a year
Must be able to work in a Labor/Management Partnership environment.
Adheres to compliance and privacy/ confidentiality requirements and standards. Adheres to GCP and compliance regulations for clinical trials.
Acquires and maintains knowledge of KP systems and databases.
Minimum one (1) year of experience coordinating research projects under specific guidance.
Minimum one (1) year of training and/or experience in research methodology/research study design, hypothesis testing; OR
Minimum one (1) year of experience in clinical trials protocols involving research methodology/research study design, and hypothesis testing; OR
Project Associate (Remote), Clinical Trials Office
By University of Virginia At National, MD, United States
Experience with the following computer applications: OnCore, EPIC, Advarra EDC, other clinical trial management systems and electronic data capture system.
Assist PI and CTO Project Managers in incorporating multi-site requirements/aspects into a developing protocol.
Supporting CTO Project Managers With Study Study Monitoring and Management:
Manage SAE/DLT information. Prepare and submit reports to the FDA, drug manufacturer and/ or participating sites, as applicable.
2-4 years of experience as a Clinical Research Coordinator (CRC), Clinical Research Associate (CRA) and/or Research Project Associate.
Working knowledge of state and federal guidelines as they apply to the conduct of clinical research.
Project Associate (Remote), Clinical Trials Office
By The Rector & Visitors of the University of Virginia At , $65,000 - $75,000 a year
Assist PI and CTO Project Managers in incorporating multi-site requirements/aspects into a developing protocol.
Supporting CTO Project Managers With Study Study Monitoring and Management:
Manage SAE/DLT information. Prepare and submit reports to the FDA, drug manufacturer and/ or participating sites, as applicable.
2-4 years of experience as a Clinical Research Coordinator (CRC), Clinical Research Associate (CRA) and/or Research Project Associate.
Working knowledge of state and federal guidelines as they apply to the conduct of clinical research.
Knowledge of GCPs governing clinical research.
Clinical Trials Associate - Cancer Institute
By Bayhealth At Dover, DE, United States
Evaluates patients’ progress toward attaining expected outcomes. Demonstrates the ability to reflect knowledge of current professional practice standards, laws and regulations.
All other duties as assigned within the scope and range of job responsibilities
Education Master Degree Master Degree Master Degree Science Health Care Related field
Credential Certified Clinical Research Associate
Clinical Trials Research Associate - Cancer Center
By University of Iowa At Iowa City, IA, United States
Minimum 1 year of clinical research experience or medical research data management experience.
Bachelor’s degree or an equivalent combination of education and experience.
Assists in the design, development, execution and administration of data entry for protocols and clinical studies.
Follows study participants; manages collection of data including maintaining records of patient visits/interviews.
Excellent verbal, written and interpersonal communication skills.
Ability to manage complex information with attention to detail and a high level of accuracy
Clinical Research Associate I - Clinical Trials Office
By Cedars-Sinai At West Hollywood, CA, United States
Participates in required training and education programs
1 year Clinical Research Related Experience preferred
Evaluates and abstracts clinical research data from source documents.
Ensures compliance with protocol and overall clinical research objectives.
Completes Case Report Forms (CRFs).
Enters clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors.
Clinical Trials Associate - Early Phase
By Worldwide Clinical Trials At United States
Generate and distribute minutes for a range of project related meetings, including Sponsor and Internal Management
Degree level qualification or equivalent experience plus a minimum of one years’ experience in a related role
Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.)
Strong organizational and problem-solving skills
Excellent skills in MS Office applications including Outlook, Word, Excel and PowerPoint
Knowledge and understanding of ICH, GCP, and FDA or EU directive regulations (as applicable)
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 Trials Associate- Oncology
By Worldwide Clinical Trials At United States
Generate and distribute minutes for a range of project related meetings, including Sponsor and Internal Management
Degree level qualification or equivalent experience plus a minimum of one years’ experience in a related role
Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.)
Strong organizational and problem-solving skills
Excellent skills in MS Office applications including Outlook, Word, Excel and PowerPoint
Knowledge and understanding of ICH, GCP, and FDA or EU directive regulations (as applicable)
Associate Director, Clinical Data Management
By IQVIA At , Remote

We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe

Clinical Trials Research Associate - Gastroenterology/Hepatology
By The University of Iowa At , Iowa City, Ia
Protocol Development/ Management and Study Responsibilities:
Excellent time management skills and the ability to perform detail oriented work independently is required
Experience with following specific protocol techniques and management is desirable.
Manage and organize regulatory documentation from sites and regulatory authorities.
Manage and organize regulatory documents from sponsors and CROs.
Excellent written and verbal communication skills are required.
Associate Director, Clinical Data Management
By Lyra Therapeutics At Watertown, MA, United States
Professional communication skills, and excellent problem-solving, organizational and project management abilities
Strong computer skills, including database management software, reporting tools, medical coding tools, etc.
Proven competence in managing delivery of multiple projects/programs independently through full data management study life cycle
Develop a strong partnership with vendor Lead Data Managers to ensure program level deliverables are on track
Prior inspection and major (vendor) audit experience a plus
Experience with EDC and ePRO systems/devices and the implementation of such systems
Clinical Trials Manager Jobs
By SPARK Neuro At United States
● Knowledge of clinical operations, project management tools and processes.
● Delegates and manages tasks and responsibilities to other team members assigned to the study
● In collaboration with data management, facilitates ongoing data review in preparation for interim,
judgment along with the ability to recommend business alternatives to senior management
This is a remote position with occasional travel.
● At least 6 years of clinical research experience including at least three (3) years having effectively
Clinical Trials Administrator Jobs
By Weill Cornell Medicine At , New York, 10065, Ny $86,200 - $110,600 a year
Experience with regulatory, data management, and billing compliance aspects of clinical research.
Approximately 3 years of experience in health-related role, in clinical or research setting.
Experience with conducting and carrying out protocols and research coordination.
As required under NYC Human Rights Law Int 1208-2018 - Salary range for this role when Hired for NYC Offices
Serves as liaison with the Food and Drug Administration (FDA), as indicated, to obtain Investigational New Drug (IND) number or exemption.
Assists leadership with developing and implementing strategies to build and grow the program's clinical research portfolio.
Clinical Trial Associate (Site Management Associate) - Home-Based
By ICON At , Remote $57,800 - $83,200 a year
Typically requires 2 year of relevant work experience in the biopharmaceutical industry, or the equivalent combination of education and experience.
Basic working knowledge of GCP, CFR and ICH guidelines and clinical trial operations
Written, verbal and interpersonal skills to exchange straightforward information
Organizes Study Team meetings and prepares meeting minutes
Assists with organizing Investigator Meetings
Assists with preparation and review of study documents
Principal Biostatistician - Respiratory / Asthma Clinical Trials (Remote, Europe/South Africa)
By Cytel, Statistical Serv and SW UK Limite At , New York, Ny

Minimum Education and Work Requirements:

Clinical Trials Nurse Ii - Cts
By Memorial Sloan Kettering Cancer Center At , New York, 10017, Ny $87,300 - $139,800 a year
Perform patient assessment, offer patient education and patient/family support
A minimum of 2-5 years of oncology nursing experience required
Clinical research nursing experience highly preferred
Providers of compassionate, evidence-based nursing care to Oncology patients and families living with cancer in a healing and innovative environment.
Committed and eager to embrace new opportunities and tough challenges with a sense of urgency, high energy, and passion.
A good decision-maker, with proven success at making timely decisions that maintain high standards of nursing care within the organization.