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Clinical Trials Specialist Jobs

Remote Clinical Trials Manager - 210641
By Medix™ At United States
Possess a minimum of 7 years of clinical trial management experience, with a focus on recent Oncology trials.
Train team members and partners, maintain study files, provide regular updates to management, and ensure compliance with GCP.
Lead study teams, foster relationships with external partners (CROs, labs, IRBs, sites), and identify/manage risks.
Assist in site selection, create RFPs, negotiate contracts, manage budgets, and oversee invoicing.
Show experience in international trials and managing external providers, including CROs.
Efficiently oversee clinical trials, managing multiple studies within a development program.
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
Clinical Trials Document Specialist Ii
By Fred Hutch At Seattle, WA, United States
Minimum 3 years of document management experience.
5+ years of document management experience
Experience working with clinical electronic databases, preferably Medidata Rave
Experience in organizing documents for internal and external audits
Facilitate the design and development of data collection forms, instructions and procedures.
Develop and maintain flow diagrams developed to document coding processes around eligibility and randomization.
Oncore Compliance Analyst (Varying Levels - Remote), Clinical Trials
By University of Virginia At National, MD, United States
Experience working with a clinical trial management system (CTMS)
In addition to the above job responsibilities, other duties may be assigned.
Experience in clinical research and/or clinical compliance
Aid in executing compliance program components, including protocol review, record keeping, reporting, and evaluation.
Perform preliminary review of protocols and identify potential concerns, reporting them to supervisor.
Work with study teams to build calendars within research systems based on research protocols.
Clinical Trials Manager/Sr Clinical Trials Manager
By Medix™ At Gaithersburg, MD, United States
At least 5 years of clinical trial management experience; Recent Oncology trial
Effective trial management of a clinical study or multiple studies within a clinical
Management of the study team for assigned studies or programs and of relationships with
Provide management with routine updates regarding the status of ongoing studies
Understanding of cross-functional areas including data management / biostatistics,
Brochures, Study Manuals, Statistical Analysis Plans, CRFs, Data Management Plans, and
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.
Clinical Trials Nurse – Sarcoma Outpatient Setting, Nyc
By Memorial Sloan Kettering Cancer Center At , New York, 10017 $87,300 - $139,800 a year
Perform patient assessment, offer patient education and patient/family support
Three years clinical Nursing experience
Clinical research nursing experience preferred but not necessary
Providers of compassionate, evidence-based nursing care to Oncology patients and families living with cancer in a healing and innovative environment
Action-oriented and eager to embrace new opportunities and tough challenges with a sense of urgency, high energy, and enthusiasm.
A good decision-maker, with proven success at making timely decisions that maintain high standards of nursing care within the organization.
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.
Senior Project Manager, Rwe Clinical Trials, Remote
By WALGREENS At , Deerfield, 60015 $143,460 - $196,010 a year
Bachelor’s degree in Life Sciences or related field and at least 4 years of clinical research and project management experience
Knowledge of clinical trials, and experience applying applicable clinical research regulatory requirements (ie. GCP and ICH guidelines)
Knowledge of project finances including experience managing, contractual obligations and implications
Knowledge of EDC systems and technology enabled solutions (EMR/Health Record Experience, Hybrid trials) with respect to use in clinical trials.
May manage a team as and when required
Identify changes in scope and manage the change control process, as necessary
Clinical Trials Operations Specialist
By McInnis Inc. At United States
Desired Experience, Skills and Abilities:
Enter country level information in BI Clinical Trial Management System (CTMS) and related systems.
Under the direction of the CTL/CTM or Feasibility Manager (depending on the task/activity), the CTO will:
Create trial specific slide decks, training material, etc. in accordance with BI requirements.
Excellent communication skills (written and oral)
In addition to the CTO responsibilities and duties, they may provide assistance in leading the trial team:
Clinical Trials Research Nurse
By Premier Health At , Centerville, 45459, Oh
Current CPR certification required at the time of hire.
1 - 3 years of job-related experience
Effective interpersonal and communication skills
Must be able to multitask with constant interruptions while maintaining a pleasant demeanor.
CLINICAL TRIALS RESEARCH NURSE / RN
Full Time 8am-4:30pm / 80 Hours per Pay
Project Manager, Rwe Clinical Trials (Remote)
By Walgreens At Deerfield, IL, United States
Bachelor’s degree in Life Sciences or related field and at least 2 years of clinical research and project management experience
Knowledge of clinical trials, and experience applying applicable clinical research regulatory requirements (i.e. GCP and ICH guidelines)
Knowledge of project finances including experience managing, contractual obligations and implications
Knowledge of EDC systems and technology enabled solutions (EMR/Health Record Experience, Hybrid trials) with respect to use in clinical trials.
Identify changes in scope and manage the change control process, as necessary
Experience collaborating with others to deliver results to meet timeline, metrics and budget.
Clinical Trials Research Assistant - Pediatric Neonatology
By University of Iowa At Iowa City, IA, United States
Bachelor’s degree in a related field or an equivalent combination of education and/or related experience.
Communicates with Research Manager and PIs about the status of the research projects.
Communicates with Research Manager and PI about the status of the research projects.
Excellent written and verbal and interpersonal communication skills.
Ability to manage complex information with attention to detail and a high level of accuracy.
Six months to one year of experience in clinical research
Administrative Services Coordinator - Clinical Trials Unit
By Kennedy Krieger Institute At Baltimore, MD, United States
Schedule meetings as requested by the Manager of Medical Program Operations, faculty members, and CTU staff.
Develops, implements, and maintains efficient and effective systems for handling departmental administrative and clerical functions.
High School diploma or GED required.
AA or equivalent college-level program, business school degree, preferred.
Clinical Trials And Site Operations Manager
By Re:Cognition Health At Chicago, IL, United States
Operations Management: 2 years (Required)
The successful applicant will have access to all Re:Cognition Health’s benefits.
Chicago, IL 60611: Reliably commute or planning to relocate before starting work (Required)
Clinical Trials Coordinating: 3 years (Required)
Clinical research: 4 years (Required)
The post holder is responsible for:
Clinical Trials Specialist Jobs
By Vitalief Inc. At New Brunswick, NJ, United States
Needs to be communicative and responsive and know when to escalate and communicate issues to management.
Oncology clinical research experience is required.
Any experience working with solid tumors is a big plus.
Demonstrated computer skills with Microsoft Office applications.
Vitalief is offering a $3,500 sign-on bonus for this position!
You'll impact clinical research in various therapeutic areas, including oncology, and improve outcomes for diverse populations.
Travel & Trials Event Specialist
By Kirkland & Ellis At Los Angeles, CA, United States
Manage and effectively communicate Firm’s travel needs to vendors/resources.
Work on developing internal processes to enhance travel experience for attorneys and staff.
A minimum of 5 years of experience in travel or hotel sales and a Bachelor’s Degree.
Establishment and promotion of strong working relationships with external contacts and suppliers to ensure the Firm’s needs are understood and met.
Creation and dissemination of travel resource communication to the Firm.
Develop relationships with paralegals to assist with their trial related travel needs including contracting hotel guest room and meeting space.
Clinical Trials Data Specialist
By Stanford University School of Medicine At Stanford, CA, United States
Knowledge, Skills And Abilities (required)
Experience with Electronic Data Capture (EDC)
Some knowledge of medical terminology
Strong clerical, interpersonal, and organizational skills.
Ability to exercise judgment and employ basic reasoning skills.
Extraction and entry of required clinical data from medical records and patient research charts/reports to Clinical Research Forms (eCRFs/CRFs).
Farm Trials Coordinator Jobs
By GrowUp Farms At Sandwich, MA, United States
Liaising with the Leaf Lab and Data teams to improve data collection and monitoring capabilities at the farm.
£30,000 onwards depending on experience
Employee benefits programme with Bravo Benefits.
All The Responsibilities We Will Trust You With
You understand commercial plant and food production environments.
You can plan, implement, and collect data from trials.
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

Are you looking for a challenging and rewarding career in clinical trials? We are seeking a Clinical Trials Specialist to join our team and help us develop and execute clinical trials that will make a difference in the lives of patients. If you have a passion for clinical research and a commitment to excellence, this could be the perfect job for you!

Overview A Clinical Trials Specialist is a professional who is responsible for the coordination and management of clinical trials. They are responsible for ensuring that the clinical trial is conducted in accordance with the protocol and applicable regulations. They are also responsible for the collection and analysis of data, and for the preparation of reports and presentations. Detailed Job Description A Clinical Trials Specialist is responsible for the coordination and management of clinical trials. This includes the development of protocols, the selection and recruitment of study participants, the collection and analysis of data, and the preparation of reports and presentations. The Clinical Trials Specialist is also responsible for ensuring that the clinical trial is conducted in accordance with the protocol and applicable regulations. Job Skills Required
• Knowledge of clinical trial protocols and regulations
• Excellent organizational and communication skills
• Ability to work independently and as part of a team
• Knowledge of data analysis and statistical methods
• Ability to manage multiple projects simultaneously
• Ability to work under pressure and meet deadlines
Job Qualifications
• Bachelor’s degree in a related field such as biology, chemistry, or health sciences
• Previous experience in clinical research or clinical trials
• Knowledge of Good Clinical Practice (GCP)
• Knowledge of medical terminology
• Knowledge of computer software programs such as Microsoft Office
Job Knowledge
• Knowledge of clinical trial protocols and regulations
• Knowledge of data analysis and statistical methods
• Knowledge of Good Clinical Practice (GCP)
• Knowledge of medical terminology
• Knowledge of computer software programs such as Microsoft Office
Job Experience
• Previous experience in clinical research or clinical trials
• Experience in project management
• Experience in data collection and analysis
Job Responsibilities
• Developing clinical trial protocols
• Recruiting and selecting study participants
• Collecting and analyzing data
• Preparing reports and presentations
• Ensuring that the clinical trial is conducted in accordance with the protocol and applicable regulations
• Maintaining accurate records of the clinical trial
• Monitoring the progress of the clinical trial