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Remote Clinical Research Associate Jobs in Union, Arkansas

Clinical Research Associate Ii (Home-Base)
By Talentify.io At United States
Utilize systems and technology for account management tasks
Remote work-from-home position with flexible schedules
Comprehensive benefits package including medical, dental, vision, and life insurance
Excellent communication skills, both written and oral
Basic knowledge of Microsoft Office Suite and Windows operating system
Strong problem-solving and conflict resolution skills
Research Analyst - Partial Remote ($70000.00 - $80000.00 / Year)
By Talentify.io At United States
Execute all phases of customer experience, including communication, project management, and negotiation of renewals and upsells.
3-5 years of experience in Customer Success or Account Management.
Excellent time management and organizational skills with strong attention to detail.
Manage a book of business, focusing on revenue growth and retention while providing exceptional customer experience.
Excellent communication skills, both written and verbal, with strong presentation abilities.
Generous stock option package, unlimited paid vacations and sick leave policies, and medical/dental benefits.
Clinical Research Monitor (Remote, Southwest Region) Tmtt
By Edwards Lifesciences At Pueblo-Cañon City Area, United States
3 years of previous clinical research field monitoring experience OR, quality assurance/control and regulatory compliance experience, required
Experience working in a medical device or regulated industry, preferred
Experience with electronic data capture, preferred
Excellent written and verbal communication skills, presentation skills, interpersonal skills, and analytical skills are required
Demonstrated problem-solving and critical thinking skills
Understanding of medical device regulatory requirements and documents, device accountability and adverse events reporting
Clinical Research Associate I
By Exact Sciences At United States
Excellent organizational, time management, and problem-solving skills.
Support and comply with the company’s Quality Management System policies and procedures.
Basic proficiency of ICH GCP and monitoring practices with a track record for ensuring quality data and performing outstanding site management.
Supports the Clinical Study Manager to develop study-specific training materials.
Conducts thorough site qualifications visits. Ensures all required information concerning site/staff qualifications is clearly documented and communicated to project teams.
Works with clinical study manager to manage vendors (ie. Central Laboratory, CRF printers, CROs, etc).
Clinical Research Associate Jobs
By Pragmatic At United States
Extensive knowledge of clinical trial procedures, GCP, and regulatory requirements
Excellent attention to detail, strong multitasking abilities, and effective communication skills
Experienced CRA Consultant - Midwest Region | Join a Leading Medical Devices Research Team!
Manage adverse events and ensure proper reporting according to industry standards
Stay abreast of the latest clinical trial processes, GCP, and regulatory requirements
Minimum of 5 years' experience as a CRA, preferably in medical devices
Clinical Research Associate - Southeast (Remote) ($88480.00 - $139100.00 / Year)
By Talentify.io At United States
Skilled in calendar management and scheduling
Knowledge of internet marketing including email and forum management
Possess strong administrative and organizational skills
Ability to multitask and perform data entry and analysis
Experience in minutes and notes taking
Knowledge of telephone and conference calling
Clinical Research Associate - Southeast Region (Remote) ($88480.00 - $139100.00 / Year)
By Talentify.io At United States
Develop and implement contract management policies and procedures
Manage contracts, global IP portfolio, and litigation matters
Register copyrights and manage annuity payments
Manage all aspects of legal holds and maintain reporting on litigation matters
Manage relationship with insurance providers about claims
Completion of paralegal school/certification highly desired
Lead Research Associate-Public Health - Remote
By Talentify.io At United States
Project Management Professional (PMP) certification
Organization skills, including time management ability and attention to detail
Demonstrated communication and collaboration skills with teams, managers, and/or clients
Demonstrated experience in program evaluation and health equity, engaging community members and partners, and/or community organizing
Professional or personal experience in/with Tribal or Indigenous communities or other marginalized populations
Experience working on federally funded projects or collaborating with academic institutions
Research Analyst - Clinical Research - Remote
By Talentify.io At United States
Strong organizational and time management ability.
Manage the study website, update content, and respond to queries from external investigators and NIH clients.
Prepare documents and power points, draft reports, and manage IRB submissions for multiple sites.
Minimum of 2 years of job experience in clinical/scientific research.
Excellent communication and collaboration skills.
Support research committees by organizing virtual and in-person meetings, preparing agendas, materials, meeting minutes, and action items.
100%Remote Role || Clinical Research Specialist
By Cloud Space LLC At United States
Skills & Experience (top 3 skills):
•Quality Management System/Regulatory Compliance Program
Location:100% remote – EST support Henry Ford in Detroit (Remote)
Work Experience (do not edit):
•Regulatory certification from AAAHRP, SOCRA, PRIM&R or similar organizations
Insert major accountabilities in chart
Senior Clinical Research Associate
By Apsida Life Science At United States
• Great career progression opportunities into management roles.
• Must be detail-oriented and efficient in time management;
This organisation will offer you the following and much more:
• Limitless training and development programs to benefit career advancement
• Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol
• Assessing the clinical research site’s patient recruitment and retention success and offering suggestions for improvement
Clinical Research Associate Ii
By Reflow Medical At United States
SPECIAL SKILLS, ABILITIES, AND REQUIREMENTS
Coordinates and manages the activities of investigative sites to ensure compliance with study protocol requirements
Supports device management, including device accountability, at the site and Sponsor level
Advanced knowledge and experience with GCP/ICH and local regulations
Experience in web-based data collection applications, knowledge of key areas of Compliance
Previous field monitoring experience required, monitoring of device trials in the cardiovascular space preferred
Research Associate - Communications Coordinator - Remote ($63100.00 - $74800.00 / Year)
By Talentify.io At United States
A minimum of 5 years of demonstrated experience with project coordination and/or project management.
Working experience with content management.
Organization skills, including time management ability
Collaboration with teams, managers and/or clients
Subject To Plan Requirements, Employees May Participate In
Provide logistic support to meet various client requests.
Associate Project Research Manager - Remote ($67800.00 - $133100.00 / Year)
By Talentify.io At United States
Coordinate data collection activities, including subcontractor contracts, finances, performance management
Manage project plans, timelines, financials (revenue, invoices, budget,) scope, quality, and compliance
Provide timely and accurate status reporting of milestones, risks, and finances to key stakeholders
3+ years in a client-facing, project managemen
Act as primary coordinator for study sponsor, study team and other internal/external third parties (e.g., research partners, IRB, vendors, clinicians)
Identify all necessary reviews and approvals and facilitate study submission in collaboration with project team
Clinical Research Associate Jobs
By Mindlance At United States
Education, Qualifications, Skills and Experience
• Good financial management skills.
• Basic change management skills.
• Support SMM in different initiatives (local, regional or global) as agreed with the SMM Line Management.
• Excellent understanding of Clinical Study Management and study start-up
• Bachelor degree in related discipline, preferably in life science, or equivalent qualification.
Clinical Research Associate I-Neurosurgery-13001-001
By Mount Sinai Health System At United States
Work with ARO data management team to ensure that all external sites have appropriate access to REDCap and Florence eBinders
1-2 years of relevant clinical research experience, preferably at least 1 year clinical trial monitoring or CRC experience
Background in clinical trial experience required
Experience working with CTMS and eTMF systems
Meet expected timelines for completion of monitoring activities and submission of written monitoring reports
Provide recommendations and guidance to study specific teams and assist in audit readiness and preparation
Research Associate-Healthcare Communications (Remote) ($70000.00 - $88500.00 / Year)
By Talentify.io At United States
Previous experience leading communications tasks for federal research contracts and/or health services research projects, and project management skills.
Project or task management experience demonstrating the ability to lead work activities.
Organization skills, including time management ability.
At least 3 years of work experience in relevant areas.
Skillful using MS Office software (Word, Excel, PowerPoint)
Excellent communication and interpersonal skills.
Contract Clinical Research Associate
By EPM Scientific At United States
Ensure protocol and regulatory compliance, quality of data, and clinical site staff training, manage study sites
Knowledge of GCP and ICH guidelines required
The CRA should have the following Qualifications…
Bachelor’s degree in a relevant scientific discipline or equivalent
Job Title: Contract Clinical Research Associate
Salary: $70 USD - $85 USD Per Hour
Research Associate I/Research Associate Ii (Remote)
By OCHIN, Inc. At United States
Demonstrated experience in complex project management and working on a project team.
Working knowledge of research and project management software preferred (e.g., REDCap, EndNote, Zotero, Smartsheet, Microsoft Suite, Twilio, etc.).
Detail-oriented and organized approach to project management.
Manages day-to-day operations of research projects and networks under the supervision of Project Director and/or Lead Investigator.
Manages day-to-day operations of complex research projects and networks. Exercises judgement in taking independent action and seeks advice when appropriate.
Working knowledge of medicine, public health, and health services issues relevant to the application of research.
Remote Claims Research Associate ($16.50 / Hour)
By Talentify.io At United States
1-2 years prior customer facing experience required
Excellent verbal and written communication skills
Establish fair market value of vehicles assisting insurers in claim settlement
Update vehicle information and determine the availability and price of new or used vehicles
Some outbound calling (non-sales related) required to automobile dealerships and adjusters
Maintain relationships with dealers and claim adjusters

Are you looking for a unique opportunity to make a difference in the healthcare industry? We are seeking a Remote Clinical Research Associate to join our team and help us develop innovative treatments for patients. You will be responsible for monitoring clinical trials, ensuring compliance with protocols, and providing support to investigators and sponsors. If you have a passion for clinical research and want to make a real impact, this is the job for you!

Overview A Remote Clinical Research Associate (CRA) is a professional who is responsible for the management and coordination of clinical trials. The CRA is responsible for ensuring that the clinical trial is conducted in accordance with the protocol, applicable regulations, and Good Clinical Practices (GCP). The CRA is also responsible for monitoring the progress of the clinical trial, ensuring that the data collected is accurate and complete, and reporting any adverse events or other issues to the sponsor. Detailed Job Description

The Remote Clinical Research Associate is responsible for the management and coordination of clinical trials. This includes:

• Developing and maintaining relationships with clinical sites and investigators
• Ensuring that the clinical trial is conducted in accordance with the protocol, applicable regulations, and Good Clinical Practices (GCP)
• Monitoring the progress of the clinical trial
• Ensuring that the data collected is accurate and complete
• Reporting any adverse events or other issues to the sponsor
• Assisting in the preparation of regulatory documents
• Assisting in the preparation of clinical study reports
• Assisting in the preparation of data for submission to regulatory authorities
• Assisting in the preparation of presentations for investigators and other stakeholders
• Assisting in the preparation of training materials for investigators and other stakeholders
• Assisting in the preparation of budgets and contracts
• Assisting in the preparation of study materials
• Assisting in the preparation of study protocols
• Assisting in the preparation of informed consent forms
• Assisting in the preparation of study reports
• Assisting in the preparation of study databases
• Assisting in the preparation of study manuals
• Assisting in the preparation of study monitoring plans
• Assisting in the preparation of study closure documents
Job Skills Required
• Excellent communication skills
• Strong organizational skills
• Ability to work independently and as part of a team
• Ability to manage multiple tasks and prioritize workload
• Knowledge of clinical trial regulations and Good Clinical Practices (GCP)
• Knowledge of clinical trial processes and procedures
• Knowledge of clinical trial data management
• Knowledge of clinical trial software
• Knowledge of medical terminology
• Knowledge of medical devices
• Knowledge of clinical research terminology
Job Qualifications
• Bachelor’s degree in a related field
• At least two years of experience in clinical research
• Certification as a Clinical Research Associate (CRA)
Job Knowledge
• Knowledge of clinical trial regulations and