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Clinical Research Trials Coordinator Jobs in Erie, Ohio

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.
Clinical Research Coordinator Ii
By University of Alabama at Birmingham At , Birmingham

Work Arrangement (final schedule to be determined by the department/hiring manager): Remote/Hybrid Eligible

This position will be responsible for research activities and research documentation processes.

Clinical Research Coordinator I
By University of Alabama at Birmingham At , Birmingham, Al
Excellent organizational skills with great attention to detail.
Written and verbal Communication skills.
Effective interpersonal and communication skills.
Work Arrangement (final schedule to be determined by the department/hiring manager)
Recruits participants for clinical trial studies.
Performs quality analysis translates data for both internal and external stakeholders.
Research Data Assistant - Clinical Trials (Full Time, Day Shift)
By Nicklaus Children's Hospital At , Miami, 33155
High School education or equivalent
Assists study staff with any concerns or questions by promptly providing the information and feedback as requested
Enters data in databases, generates reports, performs data/database maintenance, performs data tracking, and performs queries.
Provides auditable trail of documentation with consistency among data base, records and required reports
Provides reports on grant progress and assists in troubleshooting
Serves as liaison for Research Institute with all departments involved with the study.
Clinical Research Coordinator Jobs
By Shriners Children's At Dayton, OH, United States

Shriners Children’s is a family that respects, supports, and values each other. We are engaged in providing excellence in patient care, embracing multi-disciplinary education, and research with global ...

Clinical Research Coordinator Jobs
By Actalent At New Hampshire, United States
Understands and supports all of aspects of the study operations (including subject management/regulatory) with oversight from the investigator or their designee.
Bachelors or equivalent years of experience
2 years of relevant research experience
SOCRA/ACRP Certification or eligible for certification preferred
May carry out study visit tasks such as administering Quality of Life (QoL) questionnaires under supervision of
Maintains study and regulatory documentation.
Clinical Research Program Coordinator
By Picture Health At Cleveland, OH, United States
Strong organizational and multitasking skills, with the ability to prioritize and manage multiple projects simultaneously.
Coordinate and manage multiple research projects simultaneously, ensuring adherence to timelines and milestones.
PhD in a relevant scientific discipline (e.g., molecular biology, life sciences, etc) or equivalent work experience.
Very strong computer application skills, including the ability to handle spreadsheets, data analysis, and new cloud based tools.
Excellent communication and interpersonal skills, with the ability to collaborate effectively with diverse stakeholders.
Act as the primary point of contact for academic labs and pharmaceutical companies involved in R&D collaborations
Clinical Research Associate Coordinator
By The Ohio State University At , Columbus, 43210, Oh
Organize and maintain project records in compliance with the University and College of Nursing data management and storage requirements
Assist and manage community-recruitment and advertisements
Collect study data, including psychophysics data, and manage REDCap data
Manage IRB interactions including continuing reviews and amendments
Experience in clinical or basic human research
assist and manage community-recruitment and advertisements
Clinical Research Coordinator Ii
By Vanderbilt University Medical Center At , Nashville, Tn

Aligning with Vanderbilt Health’s Strategic Directions

Clinical Research Coordinator Ii
By Velocity Clinical Research, Inc. At Cincinnati, OH, United States
Apply project management concepts to manage risk and improve quality in the conduct of aclinical research study
Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelinesand Velocity’s SOPs
Develop, coordinate, and implement research and administrative strategies to successfullymanage assigned protocols.
Create, collect and submit regulatory documents to Sponsors and IRBs as required perprotocol, GCP/ICH regulations and IRB requirements.
Bachelor’s degree and 2 years relevant experience in the life science industry OR
Associate’s degree with 4 years relevant experience in the life science industry OR
Clinical Research Coordinator Jobs
By Oregon Health & Science University At , Portland, 97239, Or
Computer skills; strong organizational abilities; strong data management skills; ability to work independently;
1-2 years of relevant experience including volunteer or educational
Chart review, clinical schedule review, data entry and database maintenance, communication with providers and staff.
Bachelors Degree (4 yr) with major courses in field of research /No Experience, OR
AA/RN (2 yr) and 3 years of relevant experience, OR
Identifying, consenting, and tracking participants for clinical studies, high-risk surveillance trials/registries, and other studies as developed.
Clinical Research Coordinator (Ft) 8A-5P Research & Academics
By Ballad Health At , Kingsport, Tn

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Clinical Research Coordinator 2 Jobs
By University of Miami At , Miami, Fl
Skill in completing assignments accurately and with attention to detail.
Ability to analyze, organize and prioritize work under pressure while meeting deadlines.
Ability to process and handle confidential information with discretion.
Ability to work evenings, nights, and weekends as necessary.
Commitment to the University’s core values.
Ability to work independently and/or in a collaborative environment.
Oncology Research Registered Nurse, Clinical Trials
By Miami Cancer Institute at Baptist Health At , Miami, Fl $38.04 - $50.59 an hour

Estimated pay range for this position is $38.04 - $50.59 / hour depending on experience.

Clinical Research Coordinator Ii - Dr. Figueiredo
By CEDARS-SINAI At , West Hollywood, Ca $64,500 - $100,000 a year
2 (two) years of Clinical research related experience required
Organized, self-motivated with great interpersonal and communications skills; attention to detail; Excellent communication, writing and typing skills (spelling, grammar, syntax)
Conduct behavioral counseling/coaching with enrolled participants.
Maintain accurate and timely documentation (I.e. assessments, participant notes using REDCap)
Assist with the development and implementation of study protocols.
Monitor data and intervention dosage, fidelity and quality.
Clinical Research Coordinator 1 Jobs
By University of Miami At , Miami, Fl
Skill in completing assignments accurately and with attention to detail.
Minimum 1 year of relevant experience
Ability to analyze, organize and prioritize work under pressure while meeting deadlines.
Ability to process and handle confidential information with discretion.
Ability to work evenings, nights, and weekends as necessary.
Commitment to the University’s core values.
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 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
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 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 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 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 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 - 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;
Clinical Research Coordinator/Project Manager
By K2 Medical Research At Orlando, FL, United States
Strong time management and organizational skills In depth knowledge of industry regulations
Outstanding verbal and written communication skills
Excellent interpersonal and customer services skills
Prior experience in a clinical environment preferred. Experience in clinical research is ideal.
LPN, RN, or other medical licensure or certification preferred.
Strong working knowledge of GCP and FDA guidelines
Clinical Research Coordinator I
By Fred Hutch At Seattle, WA, United States
Liaise with investigators, industry sponsors, and other study teams to ensure each clinical trial under your management operates efficiently
Willingness to positively adapt to changing environments, data systems, compliance requirements and general competing priorities from internal and external sources
Minimum one year experience in a clinical research or cancer registry environment with regulatory or human research protections.
Demonstrated knowledge of how to synthesis study conduct.
Excellent organizational skills, attention to detail, ability to problem solve and to prioritize multiple competing tasks in a dynamic environment.
Collaborative focus is essential, as well as strong written and verbal communication skills, including computer skills.
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 Research Coordinator Jobs
By Yuma Clinical Trials At Yuma, AZ, United States

CRC

Junior Clinical Research Coordinator
By Axiom Resource Management At , Nellis Afb, 89191
Coordinate with study auditors, regulatory agencies, collaborators, and sponsors in management of research studies.
Must have current Basic Life Support (BLS) certification within 15 days of hire.
Superb organization skills with a high level of attention to detail.
Refined interpersonal and communication skills.
Experience working within the Military Healthcare System preferred.
Send resume and salary requirements to:
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 Coordinator Jobs
By Sundance Clinical Research At Greater St. Louis, United States

Experienced Clinical Research Coordinator (CRC)

Are you looking for an exciting opportunity to join a dynamic team of clinical research professionals? We are looking for a Clinical Research Trials Coordinator to join our team and help us develop and execute clinical trials for our cutting-edge medical products. As a Clinical Research Trials Coordinator, you will be responsible for coordinating all aspects of clinical trials, from protocol development to data collection and analysis. You will also be responsible for ensuring compliance with all applicable regulations and guidelines. If you are a detail-oriented professional with a passion for clinical research, this is the perfect job for you!

Overview:

A Clinical Research Trials Coordinator is responsible for coordinating and managing clinical research trials. This includes recruiting and enrolling participants, collecting and managing data, and ensuring compliance with all applicable regulations.

Detailed Job Description:

Clinical Research Trials Coordinators are responsible for the planning, implementation, and management of clinical research trials. This includes recruiting and enrolling participants, collecting and managing data, and ensuring compliance with all applicable regulations. They must also coordinate with other members of the research team, such as physicians, nurses, and other healthcare professionals. Clinical Research Trials Coordinators must be able to effectively communicate with participants and other members of the research team. They must also be able to interpret and analyze data, and provide feedback to the research team.

What is Clinical Research Trials Coordinator Job Skills Required?

• Excellent communication and interpersonal skills
• Strong organizational and time management skills
• Ability to interpret and analyze data
• Knowledge of applicable regulations and guidelines
• Ability to work independently and as part of a team
• Proficiency in Microsoft Office Suite

What is Clinical Research Trials Coordinator Job Qualifications?

• Bachelor’s degree in a related field
• At least two years of experience in clinical research
• Certification in clinical research (optional)

What is Clinical Research Trials Coordinator Job Knowledge?

• Knowledge of clinical research protocols and procedures
• Knowledge of applicable regulations and guidelines
• Knowledge of data collection and analysis
• Knowledge of medical terminology

What is Clinical Research Trials Coordinator Job Experience?

• Experience in clinical research
• Experience in data collection and analysis
• Experience in recruiting and enrolling participants

What is Clinical Research Trials Coordinator Job Responsibilities?

• Recruit and enroll participants for clinical research trials
• Collect and manage data for clinical research trials
• Ensure compliance with all applicable regulations and guidelines
• Coordinate with other members of the research team
• Interpret and analyze data
• Provide feedback to the research team