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Clinical Research Coordinator Associate Jobs in Montgomery, Maryland

Clinical Research Coordinator Jobs
By CAMRIS At Bethesda, MD, United States
Knowledge of clinical quality management and systems (such as Veeva, Master Control, etc.) is preferred.
Assist in the management of Division contract records. Tasks include the following:
CAMRIS International LLC offers competitive salaries and comprehensive benefits. Please submit your resume online at
Minimum of five (5) years of experience in clinical research or a related field.
Excellent communication, grammar and writing skills required.
Demonstrated superior knowledge of research protocols and clinical, scientific and/or medical terminology.
Clinical Research Coordinator Jobs
By Axle Informatics At Rockville, MD, United States
Supports the creation and management of clinical websites and web-based tools.
Manages conflicts issues that arise in clinical research setting, by utilizing strong communication and collaboration skills.
Educational Benefits for Career Growth
Assist researchers with study testing, observations data entry and other duties associated with study sessions. 5
Assesses ongoing consent through discussions with participants and reinforcement of education
Create mock ups and visualizations to illustrate to web developers how to execute web enhancements or new web requirements.
Clinical Research Associate Jobs
By Jobot At Germantown, MD, United States
Strong Benefits And Compensation Package
Clinical Research Associate opportunity in the oncology space!
Want to learn more about this role and Jobot?
Clinical Research Associate Jobs
By Technical Resources International, Inc. At Maryland, United States
Provides site management and monitoring support for sponsored clinical studies; primarily Phase I and II, with limited Phase III and IV.
Appropriately resolves issues related to trial monitoring and management with guidance from Project Manager or Clinical Trial Manager.
Performs on-site pre-study/qualification, initiation, routine, and close-out visits. Prepare site visit reports and provide assistance to site staff in resolving deficiencies.
Develop and demonstrate understanding of and apply therapeutic area knowledge to assignments and project-related issues.
Decisions are made independently and with some supervision from Project Manager or Clinical Trial Manager.
Four years of pharmaceutical, clinical, or biological research experience with at least 2 years of CRA experience
Research Associate- Communications Coordinator
By Westat At Maryland, United States

For more information, see below:

Clinical Research Associate Jobs
By Parsons At , , Md
BS in a biological science with knowledge of developing and conducting experiments involving high complexity assays.
Minimum 2 years’ research laboratory experience
4+ years research laboratory experience
Experience conducting research in entomology or related field.
Understanding of microscopic examination of specimens, preparation of laboratory reagents, sterile techniques, and basic tissue culture techniques.
This position shall be required to work weekends
Clinical Research Associate Jobs
By iCell Gene Therapeutics At Stony Brook, NY, United States
At least two years of experience as a clinical research associate
Excellent writing, editing, and communication skills
Strong Administrative and Organizational skills to support several team members
A bachelors degree in Health Sciences, Nursing or Medical Biotechnology, or Biological Sciences
Familiarity with various computer document formats, styles, and standards
· Collecting, analyzing, and recording data
Clinical Research Associate Jobs
By Integrated Resources, Inc ( IRI ) At Mountain View, CA, United States
The Clinical Research Intern will apply analytical, project management skills and enthusiasm for healthcare and commitment to improving healthcare through research.
The candidate will Product practical experience within the Clinical Research operations at ***.
Complies with established policies, health and safety regulations and requirements, procedures, and department objectives.
Bachelor's Degree in biological or life sciences or health related field OR attending/completed a clinical research certification program.
Proficient computer skills using Microsoft Office products.
May assist with follow up and closing of clinical studies.
Clinical Research Associate Jobs
By Juno Search Partners At Greater Philadelphia, United States
Able to manage multiple and competing priorities through effective organizational management skills.
Effective interpersonal skills; able to build effective relationships with study management team colleagues and business partners.
Excellent time management skills; able to accomplish established goals efficiently.
Supply chain management support may include:
Support Trial Management team member with assigned study specific projects and tasks.
Two years Clinical Research work experience, or relevant experience
Clinical Research Coordinator Jobs
By SRG At Springfield, Illinois Metropolitan Area, United States

Job Title: Clinical Research CoordinatorLocation: Springfield, IL Worksite: OnsiteJob Type: Permanent Full-Time We are searching for a permanent full-time Clinical Research Coordinator who has ...

Account Coordinator/Manager, Clinical Research
By Clinitiative Health Research At Dallas, TX, United States
Works on client clinical trial pipeline to secure study award
Persists to locate appropriate contacts for trial updates and outreach
Demonstrates basic understanding of clinical research
Acts on behalf of sites to sponsors to ensure consideration for feasibility and award
Communicates study updates to sites and other staff members
Completes multiple competing tasks in expected timelines
Clinical Research Associate Jobs
By Talencio At Greater Minneapolis-St. Paul Area, United States
Clinical Trial Collaboration: Work alongside our clinical team, focusing on site qualification, initiation, management, and data integrity.
Data Management: Oversee data activities, generate, and resolve queries, and report on study metrics including enrollment and adverse events documentation.
Regulatory Oversight: Manage investigational product accountability, monitor IRB requirements, and ensure prompt processing of regulatory documents.
Bachelor’s degree in a medical/scientific field, with 4+ years of clinical research experience (Master’s degree can substitute for 1 year).
Strong organizational, multitasking, and relationship-building abilities.
Effective communication skills and keen attention to detail.
Clinical Research Coordinator Ii
By UAMS - University of Arkansas for Medical Sciences At Little Rock, AR, United States
Bachelor’s degree plus 3 years general research experience w/demonstrated proficiency in study planning/development, study coordination/management, and/or data collection, or
Associate’s degree plus 5 years clinical research experience, w/demonstrated proficiency in study planning/development, study coordination/management, and/or data collection, or
High School diploma/GED plus 7 years clinical research experience w/demonstrated proficiency in study planning/development, study coordination/management, and/or data collection
UAMS offers amazing benefits and perks
Education discount for staff and dependents (undergraduate only)
Career Training and Educational Opportunities
Clinical Research Associate Jobs
By Lumicity At Austin, TX, United States
5+ years of CRA experience.
3+ years of experience working on oncology studies.
BS in a relevant scientific discipline.
Ability to travel and be on-site. (Austin, TX or Portland, OR).
6-month contract. - 40 hours per week. - Monday to Friday.
Austin, TX or Portland, OR
Clinical Research Coordinator Jobs
By Medasource At New York, United States
1+ years of Clinical Research Coordination experience
Resilient in recovering from setbacks and skilled at finding detours around obstacles.
Ensure data quality and integrity throughout the life of the study.
Collaborate with members of the research and care teams across MSK regarding data input.
Generate data reports and deliver to all necessary parties on the progress of the research project, database, or protocol.
Ensure all appropriate Institutional, State, and Federal regulations throughout the study are followed.
Clinical Research Coordinator Jobs
By SMCI At San Francisco Bay Area, United States
Education: BS/BA degree in a life science, health science, RN, or related field.
2+ years of professional working experience as a Clinical Research Coordinator.
Working knowledge of GCP and FDA Regulations.
Excellent oral and written communication skills.
Strong attention to detail and organizational skills.
Experience utilizing Electronic Data Capture (EDC) systems for clinical studies.
Clinical Research Coordinator Jobs
By SeattleNTC At Greater Seattle Area, United States
$25-$30 per hour depending on experience
2+ years of Clinical Research experience
Experience administering questionnaires (for example, WASI-II, other IQ assessments, MADRS, CAPS-5)
Experience with clinical research protocols, regulatory compliance, and submission processes
Mental health experience a plus
Seattle and Bellevue clinics (must be able to work at both)
Clinical Research Coordinator - Manager
By Medix™ At San Antonio, Texas Metropolitan Area, United States
Clearly and concisely document patient assessments, observations, test results and other study related information per federal regulations, protocol requirements and GCPs;
Obtain patient informed consent according to federal regulations, GCPs and IRB requirements;
Schedule and conduct patient visits according to protocol requirements and timelines;
Read, understand and is able to accomplish protocol specified patient visits and procedures;
Maintain accurate and complete written source documentation of patient visits and protocol related activities;
Accurately complete case report forms (CRFs &/or eCRFs) and/or worksheets generated by the sponsor;
Ophthalmology Clinical Research Associate
By SRG At United States
Minimum of four (4) years of experience in clinical research specifically in Ophthalmology surgical medical devices.
Experience in glaucoma devices is strongly preferred.
Knowledge of medical and ophthalmology terminology
Remotely monitor data and support clinical sites for protocol compliance and recruitment activities
Manage clinical trial close-out activities, including return of investigational product, final reconciliation of all required documentation, and EDC close-out
** Candidates must have experience in Ophthalmology Clinical Research trials to be considered!
Clinical Research Coordinator Jobs
By Yuma Clinical Trials At Yuma, AZ, United States

CRC

Clinical Research Associate Jobs
By Brain Tumor Network At Ponte Vedra Beach, FL, United States
• Maintains on-going professional education on clinical trials and research
• Minimum requirement: master’s degree in nursing/Healthcare related field
• Clinical work experience in oncology
• Excellent organizational and communications skills, with team-player proven ability to meet project deadlines
• Knowledge of data analytics
• Serves as a liaison to industry sponsored, consortium and Investigator initiated Brain Tumor Trials
Clinical Research Coordinator 046705 Jobs
By Wayne State University At , Detroit From $51,373 a year

H06 - School of Medicine

Hospital, outpatient clinic and office environments.

Clinical Research Associate Jobs
By AstraZeneca At , Wilmington, 19803
Good understanding of Clinical Study Management including monitoring, study drug handling and data management
1.5+ years of CRA experience in Cardiovascular/Metabolic, Respiratory and/or Immunology therapeutic experience
Fluent knowledge of spoken and written English
Excellent knowledge of international guidelines ICH/GCP, basic knowledge of GMP/GDP
Good knowledge of relevant local regulations
Good medical knowledge in relevant AZ Therapeutic Areas