Clinical Research Data Specialist
By Medasource At Nashville, TN, United States
2-3 years of experience in clinical research data entry
Strong organization and communication skills
Ensure data is correctly input into the system and quality of clinical research is maintained
Prepared for and participates in internal and external audits and action plans needed from these results.
Utilizes Query Trackers to reconcile, clarify, and complete data issues
Direct others with interpretations of rules and regulations
Clinical Research Support Specialist
By Ann & Robert H. Lurie Children's Hospital of Chicago At Streeterville, IL, United States
Supplemental Life, AD&D and Disability
Critical Illness, Accident and Hospital Indemnity coverage
Student loan servicing and support
Employee Assistance Program, and other specialized behavioral health services and resources for employees and family members
Discount on services at Lurie Children’s facilities
Clinical Research Lab Specialist
By AnMed Health At Anderson, SC, United States
Excellent computer and electronic database management skills.
Must possess excellent communication and interactive skills (both verbal and written), while also remaining flexible in responsibilities and work schedule.
Must maintain current certification for compliance and hazardous transport (IATA training).
Clinical Research Specialist, (Irvine)- Thv
By Edwards Lifesciences At Irvine, CA, United States
Experience in clinical site monitoring, site qualification, and site educational training
Partner with cross-functional team (e.g., clinical data management, field teams) with query management, data reviews and resolution
3 years of previous experience with regulatory documentation for clinical studies, required
Experience in cardiac clinical research
Sponsor industry experience with clinical trial operations/research
Experience in Medical device trial
Clinical Research Analyst *Remote*
By Talentify.io At United States
Communicate extensively with various stakeholders to manage research activities including billing compliance, budgeting, subject tracking, data collection, and sponsor invoicing.
Bachelor's Degree in a health-related field or 4 additional years of related experience.
Three years of IRB, regulatory, or research experience (4 years preferred).
Three years of relevant CTMS experience.
This is a remote position that can be based in any Providence state approved location in the US.
Review clinical research protocol documents and replicate the protocol schedule of events in Velos EResearch CTMS.
Clinical Research Trainer - Remote ($59000.00 - $91500.00 / Year)
By Talentify.io At United States
Deliver engaging and logical CRA-sponsored training remotely
Excellent planning and prioritization skills aligned with organizational goals
Develop and update CR education tools and course materials
Schedule MSK-wide CR educational courses for staff
High School Diploma and 2-5 years of relevant experience in training, mentorship, or clinical research
Knowledge of training design, medical terminology, and oncology concepts preferred
Health Disparities Clinical Specialist, Remote
By The ACI Group, Inc. At United States
Knowledge of care delivery transformation or practice redesign efforts to improve patient experience and outcomes, including ambulatory care settings
100% Remote (Must be able to work EST)
Due to our government client requirements, we can only consider US Citizens or a Green Card holders for this position
Experience with designing, implementing, or supporting clinical programs to support addressing SDoH
Knowledge of quality and utilization measure performance tied to payment
Knowledge of primary care delivery challenges and transformation opportunities
Research Specialist - Remote
By Talentify.io At United States
Opportunity to work with a full-service consulting firm that blends creative thinking with technical skills
Remote work with occasional travel to client office in Rockville, MD
Master's degree in behavioral or social science and 2+ years of experience in quantitative research field
US Citizenship required as part of client contract requirement
Experience supporting senior-level Federal civilian client and managing programs for a federal client
Strong organizational and statistical analytical skills
Clinical Research Data Entry Specialist I/Ii - Remote
By Frederick National Laboratory for Cancer Research At United States
Provides data entry and management support to an assigned caseload of research protocols
To be considered for this position, you must minimally meet the knowledge, skills, and abilities listed below:
Reviews study protocols and assists in the planning and implementation of the data management aspects of clinical research projects
Possession of a Bachelor's degree from an accredited college/university, or qualifying experience in lieu of required education
Cloud–based clinical data management systems (e.g., Medidata Rave) and enrollment tracking systems (e.g., OPEN)
Works collaboratively with VRS team members, site staff, and data monitors to meet program and protocol requirements, deadlines, and deliverables
Clinical Research Specialist Jobs
By Össur At , Irvine
2+ years experience with a documentation for regulatory compliance of medical devices, clinical research, project management preferred
All training related to the quality management system is done in accordance to the Training Management Process.
Medical writer qualifications or Certified Research Associate a plus
Experience with both qualitative and quantitative research a plus
Strong collaborative and teamwork skills
We provide a flexible work environment to offer work/life balance
Associate Clinical Research Monitor (Remote) Thv
By Edwards Lifesciences At , $64,000 - $91,000 a year
Excellent written and verbal communication skills, presentation skills, interpersonal skills, and analytical skills are required
Good problem-solving and critical thinking skills
Understanding of medical device regulatory requirements and documents, device accountability and adverse events reporting
Technical writing skills (protocols, CRF development, study tools)
Good computer skills in MS Office Suite, including Word, Excel, Adobe, and ability to operate general computer software and office machinery
Experience with electronic data capture preferred
Manager, Clinical Research Administration (Remote)
By WCG At , Madison $97,200 - $136,000 a year
Attend trainings to ensure growth in general management techniques and company‐specific knowledge, as required.
Opportunities for career development with on-the-job training, certification assistance, and continuing education reimbursement
Display integrity and positive attitude when dealing with employees, management, and clients.
Volunteer Time Off to benefit the community
Must have a bachelor’s degree from an accredited college or university, or an associate degree (AA) with equivalent work experience.
Experience in providing exceptional customer service in a fast paced, proactive, results-driven, and dynamic environment.
Senior Clinical Research Specialist
By Iterative Scopes At ,
Minimum 5 years of GI clinical research coordinator experience.
Experience coordinating, evaluating, and following patients’ participation through clinical trials.
Ability to manage multiple projects, meet deadlines, and adjust priorities appropriately.
Experience with CTMS systems - preferably RealTime, Clinical Conductor, or CRIO
Some of our benefits include:
Travel to customer sites to support study site activation, drive patient screening, and standby support for randomization activities.
Solution Specialist, Safety, Clinical Research
By Verily At , Remote
10+ years of relevant experience in Enterprise sales or business development focused on SaaS, Real Word Data and scientific services.
Experience selling complex solutions and driving significant revenue growth.
Excellent communication, presentation and analytical skills.
Proven ability to work with complex, technical software and service offerings, and processes involving multiple stakeholders.
Experience with Google suite of productivity applications (gMail, gCalendar, Sheets, Slides, Docs).
Build and maintain strong relationships with customers and partners.
Clinical Research Monitor (Remote) Tmtt
By Edwards Lifesciences At Albuquerque-Santa Fe Metropolitan Area, United States
3 years of previous clinical research field monitoring experience OR, quality assurance/control and regulatory compliance experience, required
Experience working in a medical device or regulated industry, preferred
Experience with electronic data capture, preferred
Excellent written and verbal communication skills, presentation skills, interpersonal skills, and analytical skills are required
Demonstrated problem-solving and critical thinking skills
Understanding of medical device regulatory requirements and documents, device accountability and adverse events reporting
Research Strategy & Programs Specialist **Remote Available**
By Vanderbilt University Medical Center At , Nashville, 37232
The responsibilities listed are a general overview of the position and additional duties may be assigned.
Bachelor's Degree (or equivalent experience) (Required)
2 year relevant experience (Required)
Provide research support consultation and services to all levels of research colleagues.
Collaborate with internal and external customers to evaluate current services for continual improvement and the development of new research services.
Educate the research community regarding resources available to clinicians and researchers to improve all aspects of the research enterprise.
Clinical Research Coordinator Crc - Remote | Wfh
By Get It Recruit - Healthcare At Pompano Beach, FL, United States

Are you passionate about making a difference in the field of healthcare? Do you thrive on engaging with patients and ensuring top-notch research protocols? We have an exciting opening for a Clinical ...

Senior Manager, Clinical Research Monitoring (Remote)
By Edwards Lifesciences At , , Wi $123,000 - $174,000 a year
Excellent written and verbal communication skills including negotiating and relationship management skills with ability to drive achievement of objectives
Ability to interact professionally with all organizational levels and proactively escalate issues to appropriate levels of management in the organization
Provide direction and guidance to execute project deliverables in collaboration with project managers
Experience with electronic data capture preferred
Excellent problem-solving, organizational, analytical and critical thinking skills
Expert understanding of clinical studies procedures while addressing issues with impact beyond own team based on knowledge of related disciplines
Clinical Research Monitor (Remote, Midwest/Northeast Region) Tmtt
By Edwards Lifesciences At Greater Owensboro Area, United States
3 years of previous clinical research field monitoring experience OR, quality assurance/control and regulatory compliance experience, required
Experience working in a medical device or regulated industry, preferred
Experience with electronic data capture, preferred
Excellent written and verbal communication skills, presentation skills, interpersonal skills, and analytical skills are required
Demonstrated problem-solving and critical thinking skills
Understanding of medical device regulatory requirements and documents, device accountability and adverse events reporting
Clinical Research Specialist Jobs
By Mindlance At Irvine, CA, United States
• Demonstrated experience in establishing and maintaining effective relationships with management, peers and subordinates and customers.
5) What are the top 5 skills/requirements this person is required have?
• Manage and prioritize work load, multi-task and manage a diverse mix of issues, responsibilities and challenges.
a. Required Skill 1: Organized and great attention to detail
b. Required Skill 2: Strong communication skills and intrapersonal skills
c. Required Skill 3: Takes initiative and works well alone and also within a team