Research Associate I - Health Research (Remote)
By The Henry M. Jackson Foundation for the Advancement of Military Medicine At Bethesda, MD, United States
Required Knowledge, Skills And Abilities
Assists with preparation of summary documents and reports in conjunction with Program Manager and Project Manager.
Strong communications and qualitative and quantitative analytical skills, sufficient to graph data and describe results clearly and accurately.
Experience within Health Services Research preferred.
Experience in biostatistics and epidemiology.
Minimum of 0-2 years’ experience required
Dps Clinical Research Assistant I - Outcomes Research
By City of Hope At Duarte, CA, United States
Experience may substitute for minimum education requirements
Basic education, experience and skills required for consideration:
Preferred education experience and skills:
Conducts protocol management for an assigned set of multiple research protocols.
Performs data management and data analyses, as required by the research study.
Identifies and communicates important protocol and data management issues or problem areas to supervisor.
Clinical Research Associate - Sponsor Dedicated
By IQVIA At , Remote
Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.
Effective time and financial management skills.
Alternatively, you should have an equivalent combination of education, training and experience
A Bachelor's degree in a health care or other scientific discipline or educational equivalent
Good therapeutic and protocol knowledge as provided in company training.
Written and verbal communication skills including good command of English language.
Clinical Research Associate I, Dcri
By Duke University At , Durham, 27710
Review education and training experience with line manager and complete identified training needs within designated time period.
*Basic knowledge of site management and clinical monitoring for clinical research studies
Maintain job knowledge and skills through independent self-study.
OR EQUIVALENT COMBINATION OF EDUCATION AND EXPERIENCE
None required beyond that described above. OR AN EQUIVALENT COMBINATION OF RELEVANT EDUCATION AND/OR EXPERIENCE
Perform assessment of site personnel and facilities for study conduct through feasibility and site telephone qualification
Clinical Research Coordinator I
By The Geneva Foundation At , San Antonio, 78234 $43,800 - $58,800 a year
Computer skills including at least intermediate level experience with Excel and other Microsoft Office Software
Bachelors degree or equivalent work experience required
2-4 years experience in clinical research preferred
2-4 years non-profit, research, or healthcare experience desired
Knowledge of CFR, GCP and ICH guidelines
Promote safety and confidentiality of research participants at all times
Clinical Research Coordinator I
By University of Alabama at Birmingham At , Birmingham
Be organized, show attention to detail, and have exceptional follow-through abilities.
Have clinical decision-making and assessment skills, enjoy face-to-face interactions with patients and study participants, and interfacing with investigators and clinicians.
Work Arrangement (final schedule to be determined by the department/hiring manager): Onsite
To collect and record preliminary data for clinical research programs.
To recruit and perform follow-up with research participants as protocols outline.
To schedule visits according to research protocols.
Research Associate I Jobs
By Drexel University At , Philadelphia, 19104
Experience with data management in a research setting, including but not limited to tools such as REDCap or Qualtrics.
Please review the Benefits Brochure for some information on our benefits offerings.
Help maintain and manage datasets, and maintain clear and detailed documentation necessary to maintain databases and analyses.
Manage multiple research projects’ data collection timelines to keep projects on track to meet goals.
Experience with data collection with autistic individuals and/or their families, broadly defined.
Experience conducting engagement or outreach activities with families, either in a clinical, research, school-based, or community setting.
Clinical Research Associate Ii - Phoenix / Tucson
By ICON At , Phoenix
Knowledge of ICH and local regulatory authority regulations regarding drug
Experience in monitoring all trial components (PSSV to COV)
Ability to travel as needed (greater than 40%)
Research Associate I Jobs
By BAXTER At , Round Lake $52,800 - $132,000 a year
Understand and apply applicable corporate and divisional SOPs. Maintain knowledge of relevant QSR and safety requirements.
Demonstrate working knowledge of basic technical theories and principles within area of expertise for routine tasks.
Develop knowledge and understanding of GxP and related regulations and guidance.
Bachelors degree in a science-related field with 0-1 years experience
Possess relevant laboratory (chemistry)/technical, writing, and computer skills.
Employ appropriate techniques and methods to successfully conduct specific assignments within negotiated deadlines after receiving general instruction.
Clinical Research Coordinator I
By Velocity Clinical Research, Inc. At Covington, LA, United States
The Clinical Research Coodinator I conducts and manages clinical trials in accordance with the study protocol,GCP, and Velocity’s SOPs.
Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and Velocity’s SOPs
Implement research and administrative strategies to successfully manage assigned protocols.
Create, collect, and submit regulatory documents to Sponsors and IRBs as required per protocol, GCP/ICH regulations, and IRB requirements.
Bachelor’s degree with 1 year of relevant experience in the life science industry OR
Associate’s degree with 2 years of relevant experience in the life science industry OR
Clinical Research Associate (Cra)
By Peachtree BioResearch Solutions At Atlanta, GA, United States
Work closely with the Site Management team and sponsor stakeholders so you can plan and manage your work most effectively
Work with Peachtree's Data Management team and sites to ensure all queries are resolved
1-5 years of experience working on clinical trials (CRO or Sponsor) as either a coordinator or CRA I
Experience with CNS, rare disease and/or oncology studies preferred
Experience working in a CTMS and EDC system
Excellent organizational and critical thinking skills
Clinical Research Associate I - Smidt Heart Institute
By Cedars-Sinai At Los Angeles, CA, United States
Participates in required training and education programs.
1-year Clinical Research Related Experience
Join our team and use your skills with an organization known nationally for excellence in research!
Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement study.
Evaluates and abstracts clinical research data from source documents.
Ensures compliance with protocol and overall clinical research objectives.
Predoctoral Research Associate I
By Fred Hutchinson Cancer Center At , Seattle $65,484 - $100,000 a year
Conduct and oversee data collection and management; help generate study reports
Help prepare research materials (such as study protocols, questionnaires, educational materials, and data collection instruments)
High level of attention to detail, excellent organizational skills.
Excellent written skills, including academic writing skills. Outstanding interpersonal and verbal communication skills.
Strong working knowledge of Microsoft Office applications, specifically Word, Excel, PowerPoint, and Outlook.
Experience working with qualitative and quantitative data collection and analysis.
Clinical Research Associate Jobs
By Candel Therapeutics At Needham, MA, United States
Knowledge of project management tools and practices, and proficiency in using normal office software; Microsoft Word, Excel and PowerPoint.
Participate in maintaining accuracy within clinical management systems and internal reports and trackers.
Able to manage multiple projects independently and use varying databases and management systems.
Minimum 1-3 years relevant clinical research experience.
Excellent verbal and written communication skills, good organizational and interpersonal skills, and a team drive.
Knowledge of GCP and FDA regulations related to clinical trial conduct and familiarity with industry best practices.
Associate Clinical Research Associate (Remote -West Region)
By Merck Sharp & Dohme At , Rahway, 07065, Nj $72,880 - $114,600 a year
Developing skills in Site Management including management of site performance and patient recruitment
Effective time management, organizational and interpersonal skills, conflict management
Able to work with other experienced research professions to develop skills across multiple protocols, sites and therapy areas.
Coordinates & manages various tasks in collaboration with other sponsor roles to achieve Site Ready.
Manages and maintains information and documentation in CTMS, eTMF and various other systems as appropriate and per timelines.
Good understanding and working knowledge of clinical research, phases of clinical trials, current GCP/ICH & country clinical research law & guidelines.
Clinical Research Associate, Sponsor Dedicated
By IQVIA At , Remote
Alternatively, you should have an equivalent combination of education, training and experience
A Bachelor's degree in a health care or other scientific discipline or educational equivalent
2 years of clinical research coordinator experience strongly preferred
While projects vary, your typical responsibilities might include:
We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe
Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
Clinical Research Coordinator I
By Seattle Childrens Hospital At , Seattle, 98105, Wa $55,765 - $83,637 a year
Bachelor's Degree in related discipline, or equivalent combination of education and experience.
Prior experience in research or a related field/setting.
Confirmed proficiency in a second language via successful completion of a language assessment may be required for certain departments.
Min to Max Hourly Salary$26. 81 - $40.21 /hr
Min to Max Annual Salary$55,764.80 - $83,636.80 /yr
The union pay ranges can be found on the Seattle Children's website here: -
Senior Research Associate I – Biologics Discovery
By Gilead Sciences At Foster City, CA, United States
Mammalian cell culture skills required. Transient protein expression experience is a plus.
Hands-on experience performing basic in vivo rodent studies.
Experience in flow cytometry required. Experience with single-cell FACS sorting or other single-cell technologies is a plus.
Experience in molecular cloning is a plus.
Strong written and oral communication skills, with an ability to work in a dynamic, collaborative, and evolving environment.
Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.
Clinical Research Associate I (Part-Time)
By Binghamton University At Stony Brook, NY, United States

In accordance with the Title II Crime Awareness and Security Act

Clinical Research Associate Jobs
By Lyra Therapeutics At Watertown, MA, United States

Lyra Therapeutics, Inc. is a clinical-stage biotechnology company developing novel, integrated drug and delivery solutions for the localized treatment of patients with chronic rhinosinusitis (CRS) ...