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Clinical Research Trials Coordinator Jobs in Union, Arkansas

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 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 (Dr. Jessica Robinson-Papp's Lab) - Neurology
By Mount Sinai Health System At United States
Bachelors degree in science or related field preferred or a combination of relevant research experience and education
0-2 years of research/human subjects experience
Assists in the collection, analysis and review of experimental data for publication and presentation.
May secure and ship clinical specimens as required by the protocol.
May assist in the preparation for regulatory agency site visits.
Inspiring and fostering an environment of anti-racist behaviors among and between departments and co-workers.
Clinical Research Coordinator Ii-Msh-Cs03-12118-013
By Mount Sinai Health System At United States
Analyzes moderately complex clinical research data; Assists in interpreting clinical research data.
Coordinates the clinical assessments of the study subjects including but not limited to screening and evaluation of the study subjects.
Prepares and ensures grant applications, IRB/GCO documents are submitted.
Ensures accurate and complete compilation of subject data through chart reviews.
Independently obtains informed consent for other clinical studies.
Mentors Clinical Research Coordinators in training.
Clinical Research Coordinator I-Personalized Med
By Mount Sinai Health System At United States
Obtain informed consent and educate participants regarding study requirements.
1-2 years clinical research experience
Pristine attention to detail and ability to manage time appropriately, able to multitask in a fast-paced environment
Collect and record study data and input all information into a database.
Assist in IRB/GCO applications as needed.
Collect, process, deliver and ship clinical specimens as required by the protocol.
Clinical Research Coordinator-Msh/Qhc-14100-018
By Mount Sinai Health System At United States
Bachelors degree in science or related field preferred or a combination of relevant research experience and education
0-2 years of research/human subjects experience
Assists in the collection, analysis and review of experimental data for publication and presentation.
May secure and ship clinical specimens as required by the protocol.
May assist in the preparation for regulatory agency site visits.
Inspiring and fostering an environment of anti-racist behaviors among and between departments and co-workers.
Clinical Research Coordinator I-12910-049
By Mount Sinai Health System At United States
Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.
1-2 years of research experience
Collects and records study data. Inputs all information into database.
Assists in preparing grant applications, IRB/GCO for submission and filings.
Secures, delivers and ships clinical specimens as required by the protocol.
Bachelors or Masters degree in Science or closely related field.
Clinical Research Coordinator - Medicine Clinical Trials Office
By Mount Sinai Health System At United States
Bachelors degree in science or related field preferred or a combination of relevant research experience and education
0-2 years of research/human subjects experience
Assists in the collection, analysis and review of experimental data for publication and presentation.
May secure and ship clinical specimens as required by the protocol.
May assist in the preparation for regulatory agency site visits.
Inspiring and fostering an environment of anti-racist behaviors among and between departments and co-workers.
Clinical Trials Associate - Early Phase
By Worldwide Clinical Trials At United States
Generate and distribute minutes for a range of project related meetings, including Sponsor and Internal Management
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
Knowledge and understanding of ICH, GCP, and FDA or EU directive regulations (as applicable)
Clinical Research Coordinator Jobs
By Advarra At United States
Remote, onsite, and hybrid opportunities available
Clinical Research Coordinators II/III roles are consulting (contractor) roles. These are not permanent position with benefits.
The benefits of enjoying the Advarra team include:
•Current training in human subjects protection education, Good Clinical Practice, and HIPAA Privacy
Potentially higher hourly pay rate than working direct
Clinical Research Coordinator I (All Of Us)
By Mount Sinai Health System At United States
Strong communication and organization skills
Obtain informed consent and educate participants regarding study requirements.
1-2 years clinical research experience
Pristine attention to detail and ability to manage time appropriately, able to multitask in a fast-paced environment
Background in clinical research or closely related field
Passion for patient care and clinical research
Clinical Research Coordinator - Seaver Center For Autism
By Mount Sinai Health System At United States
Bachelors degree in science or related field preferred or a combination of relevant research experience and education
0-2 years of research/human subjects experience
Assists in the collection, analysis and review of experimental data for publication and presentation.
May secure and ship clinical specimens as required by the protocol.
May assist in the preparation for regulatory agency site visits.
Inspiring and fostering an environment of anti-racist behaviors among and between departments and co-workers.
Clinical Research Coordinator Ii-13400-043
By Mount Sinai Health System At United States
Analyzes moderately complex clinical research data; Assists in interpreting clinical research data.
Coordinates the clinical assessments of the study subjects including but not limited to screening and evaluation of the study subjects.
Prepares and ensures grant applications, IRB/GCO documents are submitted.
Ensures accurate and complete compilation of subject data through chart reviews.
Independently obtains informed consent for other clinical studies.
Mentors Clinical Research Coordinators in training.
Clinical Research Coordinator I - Personalized Med
By Mount Sinai Health System At United States
Obtain informed consent and educate participants regarding study requirements.
Strong communication and organization skills
1-2 years clinical research experience
Pristine attention to detail and ability to manage time appropriately, able to multitask in a fast-paced environment
Collect and record study data and input all information into a database.
Assist in IRB/GCO applications as needed.
Clinical Research Coordinator Ii-Psychiatry - Ism - Ft - Day
By Mount Sinai Health System At United States
Analyzes moderately complex clinical research data; Assists in interpreting clinical research data.
Coordinates the clinical assessments of the study subjects including but not limited to screening and evaluation of the study subjects.
Prepares and ensures grant applications, IRB/GCO documents are submitted.
Ensures accurate and complete compilation of subject data through chart reviews.
Independently obtains informed consent for other clinical studies.
Mentors Clinical Research Coordinators in training.
Clinical Research Coordinator I
By Mount Sinai Health System At United States
Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.
1-2 years of research experience
Collects and records study data. Inputs all information into database.
Assists in preparing grant applications, IRB/GCO for submission and filings.
Secures, delivers and ships clinical specimens as required by the protocol.
Bachelors or Masters degree in Science or closely related field.
Clinical Trials Associate- Oncology
By Worldwide Clinical Trials At United States
Generate and distribute minutes for a range of project related meetings, including Sponsor and Internal Management
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
Knowledge and understanding of ICH, GCP, and FDA or EU directive regulations (as applicable)
Clinical Research Coordinator - Hybrid/Remote - 122856 ($33.60 - $43.81 / Hour)
By Talentify.io At United States
Strong knowledge of investigational protocols (data management, query resolution, protocol design and protocol implementation).
Strong knowledge of investigational protocols especially with pediatric protocols (data management, query resolution, protocol design, protocol writing and protocol implementation).
Demonstrated experience in clinical trials research. Strong knowledge of experimental protocols, data gathering, protocol design and evaluation.
Demonstrated experience performing clinical research duties in a clinical research environment such as CRO, academic research institution, and/or a research hospital.
Experience in providing work direction and assisting supervisor in maintaining an efficient medical research team.
Experience with research protocol in order to screen patients for eligibility, initiate treatment plan, collect specimens, and orient participating physicians.
Clinical Trials Manager Jobs
By SPARK Neuro At United States
● Knowledge of clinical operations, project management tools and processes.
● Delegates and manages tasks and responsibilities to other team members assigned to the study
● In collaboration with data management, facilitates ongoing data review in preparation for interim,
judgment along with the ability to recommend business alternatives to senior management
This is a remote position with occasional travel.
● At least 6 years of clinical research experience including at least three (3) years having effectively
Clinical Research Regulatory Coordinator
By Medix™ At United States
Experience using standard word processing and data management software programs, including Word and Excel, in order to develop and prepare reports.
Experience creating Informed Consent Documents that comply with HRPP/ IRB policies and procedures, FDA regulations, and sponsor requirements.
Experience with editing, including summarizing information into concise and condense documents.
Knowledge of oncology and hematology.
Experience working with FDA regulations, NCI policies and procedures, and Good Clinical Practice guidelines for the conduct of clinical research.
Working knowledge of Human Research Protections Program (HRPP/IRB) policies and Procedures.

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