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Clinical Research Trials Coordinator Jobs in Lake, Illinois

Clinical Research Coordinator Jobs
By Sundance Clinical Research At Greater St. Louis, United States

Experienced Clinical Research Coordinator (CRC)

Project Manager, Rwe Clinical Trials (Remote)
By Walgreens At Deerfield, IL, United States
Bachelor’s degree in Life Sciences or related field and at least 2 years of clinical research and project management experience
Knowledge of clinical trials, and experience applying applicable clinical research regulatory requirements (i.e. GCP and ICH guidelines)
Knowledge of project finances including experience managing, contractual obligations and implications
Knowledge of EDC systems and technology enabled solutions (EMR/Health Record Experience, Hybrid trials) with respect to use in clinical trials.
Identify changes in scope and manage the change control process, as necessary
Experience collaborating with others to deliver results to meet timeline, metrics and budget.
Clinical Research Coordinator Jobs
By University of Chicago At Chicago, IL, United States
Analyzes protocols and advise treating physicians on appropriate dosage modifications or treatment calculations based on patient characteristics.
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.
Clinical Trials And Site Operations Manager
By Re:Cognition Health At Chicago, IL, United States
Operations Management: 2 years (Required)
The successful applicant will have access to all Re:Cognition Health’s benefits.
Chicago, IL 60611: Reliably commute or planning to relocate before starting work (Required)
Clinical Trials Coordinating: 3 years (Required)
Clinical research: 4 years (Required)
The post holder is responsible for:
Clinical Research Coordinator Ii
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 Coordinator - Chicago
By The IMA Group At Chicago, IL, United States
Coordinate clinical trials per FDA requirements and GCP guidelines per sponsor protocols.
Acquire detailed knowledge of the protocol and procedures associated with each clinical research study.
Maintain familiarity with each clinical research study’s requirements and apply all applicable regulations accurately.
Additional duties and responsibilities may be assigned as needed.
Strong follow through skills and ability to proactively identify and solve problems, demonstrated initiative is imperative.
Must have strong communication skills, speak, and listen respectfully with the public, physicians, and co-workers.
Clinical Research Coordinator Ii
By Ann & Robert H. Lurie Children’s Hospital of Chicago At , Chicago, 60611, Il
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
Medical, dental and vision insurance
Pediatric Clinical Research Coordinator 1
By The University of Chicago At , Chicago, 60637, Il
Strong data management skills and attention to detail.
Clinical research experience or relevant experience.
Ability to develop and manage interpersonal relationships.
Ability to learn and develop skills.
Knowledge of Microsoft Word, Excel and Adobe Acrobat.
Recruit and interview potential study patients with guidance from PI and other clinical research staff.
Clinical Research Coordinator I
By Ann & Robert H. Lurie Children's Hospital of Chicago At Chicago, IL, United States
Familiar with formulas in excel and advanced database management.
Bachelors with three to five years clinical research experience.
Strong oral and written communication skills in order to address large/diverse audiences. Strong customer service skills required.
Intermediate knowledge of Microsoft Office Suite (Excel, Work, Outlook, etc.).
Certification as a Clinical Research Professional (SOCRA) or Clinical Research Coordinator (ACRP) preferred.
Works collaboratively with all levels within the organization to advise on contractual negotiations, recommendations and processes.
Clinical Research Coordinator 2 Jobs
By The University of Chicago At , Chicago, 60637, Il
Clinical research experience or relevant experience.
Experience coordinating multiple studies (e.g., investigator initiated, industry sponsored, multi-site trials).
Ability to develop and manage interpersonal relationships.
Ability to learn and develop skills.
Recruit and interview potential study patients with guidance from PI and other clinical research staff.
Collect, process, ship and store specimens to appropriate laboratory according to established aseptic techniques.
Clinical Research Coordinator Jobs
By Ann & Robert H. Lurie Children’s Hospital of Chicago At , Chicago, 60611, Il
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
Medical, dental and vision insurance
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 Trials Manager/Sr Clinical Trials Manager
By Medix™ At Gaithersburg, MD, United States
At least 5 years of clinical trial management experience; Recent Oncology trial
Effective trial management of a clinical study or multiple studies within a clinical
Management of the study team for assigned studies or programs and of relationships with
Provide management with routine updates regarding the status of ongoing studies
Understanding of cross-functional areas including data management / biostatistics,
Brochures, Study Manuals, Statistical Analysis Plans, CRFs, Data Management Plans, and
Clinical Research Coordinator Jobs
By Rady Children's Hospital-San Diego At San Diego County, CA, United States

Job Summary: Initiates & manages multiple cooperative group trials such as Children's Oncology Group (COG) clinical trials related to pediatric cancer to include, but not limited to: execution ...

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