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Clinical Research Protocol Specialist Jobs

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 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
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 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
Protocol Administrative Assistant (Junior)
By Metropolitan Transportation Authority At Washington, DC, United States

Protocol Administrative Assistant (Junior) - Contingent Upon Contract Award MTA, Inc is a Woman-owned Small Business with headquarters located in Huntsville, AL providing a broad range of professional ...

Clinical Research Operations Specialist
By Fred Hutch At Seattle, WA, United States
Experience with Clinical Trials Management System (i.e., OnCore, Velos, etc.)
Organize and manage time and tasks independently
2 years of health care operations experience preferably in clinical research
Demonstrated skills in critical thinking and problem solving
Strong written and verbal communication skills
2 years of clinical research experience
Research Specialist (Clinical Sciences And Advanced Medicine))
By University of Pennsylvania At Philadelphia, PA, United States
Your responsibilities as the Research Specialist will include:
To learn more, please visit: https://www.hr.upenn.edu/PennHR/benefits-pay
Cell processing and tissue culture. Isolate and process fibroblasts from murine skin samples. Maintain cell cultures for differentiation assays.
Maintain mouse colonies (set up breeding, monitor health and maintain records).
Perform in vivo wound healing or tumor studies in mice.
Perform tissue fixation, embedding and sectioning for histology.
100%Remote Role || Clinical Research Specialist
By Cloud Space LLC At United States
Skills & Experience (top 3 skills):
•Quality Management System/Regulatory Compliance Program
Location:100% remote – EST support Henry Ford in Detroit (Remote)
Work Experience (do not edit):
•Regulatory certification from AAAHRP, SOCRA, PRIM&R or similar organizations
Insert major accountabilities in chart
Clinical Research Specialist, (Hybrid, Irvine)- Tmtt
By Edwards Lifesciences At Irvine, CA, United States
Experience in site monitoring/central monitoring skills, site qualification, and site training
Data management experience or analytics
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
Remote Clinical Research Specialist
By Comrise At California, United States
REMOTE Clinical Research Specialist ( Medical Device)- 6 months contract- May go perm
o Preferred, experience with electronic file system, Medidata and Sharepoint & Smartsheet.
5 + years, BA required. o Working as CRA (clinical research associate.)
o Familiar GDP (good documentation practices)
o Filling clinical trial documents ETMF
Clinical Research Specialist Jobs
By Roth Staffing At United States
Roles typically require a university degree or an extensive amount of practical knowledge gained through experience.
Must have knowledge in reference to good clinical practices regulations and standard operating procedures.
The job requires the ability to make judgements based on practice and previous experience.
Preferred, experience with electronic file system, Medidata and SharePoint & Smartsheet.
Coordinates activities of associates and investigators to ensure compliance with protocol and overall clinical objectives.
Maintains a high level of professional expertise through familiarity with clinical literature and participates in project team meetings.
Clinical Research, Imaging Specialist
By University of Chicago At Chicago, IL, United States
Manages the analysis of complex imaging data.
Coordinates and may participate in quality assurance reviews conducted by study sponsors, federal agencies, or specially designated review groups.
Analyzes study-related documentation, such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, or progress reports.
Performs other related work as needed.
Motor Vehicle Record Inquiry Required
Clinical Research Protocol Specialist
By Frederick National Laboratory At ,
Previous study coordination and/or project management experience in clinical research
To be considered for this position, you must minimally meet the knowledge, skills, and abilities listed below:
Knowledge of regulatory requirements and guidelines for facilitating clinical human subjects research, including Health and Human Services (HHS) regulations
Serves as the point-of-contact and project manager for an assigned portfolio of projects
This position is located in Rockville, Maryland. Remote work is possible.
Strong collaborative skills with ability to build relationships within multiple groups