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Clinical Research Associate Jobs in Union, Arkansas

Clinical Research Associate I- Principal
By i-Pharm Consulting At United States
Conduct all types of visits including, qualification, initiaiton, monitoring and close out
Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff
Ensure good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP, and applicable regulatory requirements
Minimum 1.5 years monitoring experience
Strong verbal and written communication skills
8-12 days on site per month
Ophthalmology Clinical Research Associate
By SRG At United States
Minimum of four (4) years of experience in clinical research specifically in Ophthalmology surgical medical devices.
Experience in glaucoma devices is strongly preferred.
Knowledge of medical and ophthalmology terminology
Remotely monitor data and support clinical sites for protocol compliance and recruitment activities
Manage clinical trial close-out activities, including return of investigational product, final reconciliation of all required documentation, and EDC close-out
** Candidates must have experience in Ophthalmology Clinical Research trials to be considered!
Clinical Research Associate/Site Manager
By Relmada Therapeutics, Inc At United States
·3+ years of clinical monitoring or site management experience.
Delivers high quality and timely reports following each site management or site monitoring visit.
May include managing query resolution process with clinical sites and data management groups.
·Thorough knowledge and understanding of ICH/GCPs and applicable regulatory requirements.
·Solid computer skills, including working knowledge of Microsoft Office applications (Word, Excel Outlook, etc.).
Prepares for and conducts site qualification and site initiation, visits. May also include interim and closeout monitoring visits.
Clinical Research Associate - Mid-West/Central - Cns/Gen Med - Home Based
By Worldwide Clinical Trials At United States
Excellent interpersonal, oral, and written communication skills in English
Superior organizational skills with attention to details
5+ years of experience as a Clinical Research Associate
Experience in CNS is required
Conduct study initiation visits (SIVs)
Ability to work with little or no supervision
Clinical Research Associate (Fsp) - Poland
By Parexel At United States
Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology.
Excellent time management and social skills
Minimum of 2 years of active independent field monitoring experience - all types of visits.
Strong interpersonal, written, and verbal communication skills within a matrixed team.
Experience working in a self-driven capacity, with a sense of urgency and limited oversight.
Benefits Of Working With Parexel FSP
Clinical Research Associate (Cra)
By LumaBridge At United States
Ability to independently prioritize tasks with excellent time management skills.
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans.
Perform other duties as assigned by management.
Excellent verbal and written communication skills and conflict resolution abilities.
Oversee and conduct monitoring activities, including remote monitoring and risk-based monitoring.
Lead assigned sites through regular contact to ensure site compliance, adequate enrollment, and understanding of study requirements.
Clinical Research Associate (Contract/Fulltime)
By ClinChoice At United States
· Prepares and attends assessment visits with less experienced CRAs, as required.
· Sound knowledge of medical terminology.
· Excellent communication in English in both written and verbal skills.
· Excellent interpersonal and organizational skills.
· Ability to manage more than 1 study simultaneously.
· Monitors activities at clinical study sites to assure adherence to GCP, ICH, SOPs, and study protocols.
Clinical Research Associate I - Hybrid/Remote
By Talentify.io At United States
Knowledge of clinical research study processes, protocol management, and regulatory guidelines.
Proficiency in medical terminology and computer skills.
Strong attention to detail and excellent written and oral communication skills.
Ability to manage multiple deadlines and prioritize tasks effectively.
Minimum three years of experience in conducting clinical research studies or verifying clinical data.
Knowledge across multiple therapeutic areas, including blood and marrow transplant.
In House Clinical Research Associate
By Premier Research At United States
Previous CRO experience preferred. An equivalent combination education and experience will be considered.
Prior experience in the conduct of clinical research including ICH-GCP requirements, drug/device development process, regulatory compliance, and study coordination preferred.
Strong written, oral communication, and organization skills and a strong attention to detail.
We are Built by You. Your ideas influence the way we work, and your voice matters here.
BS/BA degree (or its international equivalent) preferably in a scientific or health-related field.
Join us and build your future here
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
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
Senior Clinical Research Associate (Medical Device)
By ICON Strategic Solutions At United States

Ability to independently oversee sites and handle not only monitoring responsibility but also oversee site management activities

Ability to travel approximately 30% of the time nationwide

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
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
Senior Clinical Research Associate (Oncology)
By Allucent At United States
Can demonstrate experience and knowledge in the CRO industry that will support POI’s management of clinical trials.
Assist the Project Team with the day-to-day management of clinical studies as required.
Monitoring Visit Report (MVR) review, management, resolution and escalation as required.
Relevant life science degree / medical / nursing background, or combination of education and experience.
Proven organizational abilities, and excellent written and oral communication and presentation skills.
A thorough knowledge of regulatory submission and reporting requirements and guidelines.
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

Are you looking for a challenging and rewarding career in clinical research? We are looking for a Clinical Research Associate to join our team and help us develop and execute clinical studies. You will be responsible for managing clinical trials, ensuring compliance with applicable regulations, and providing support to investigators and sponsors. If you have a passion for clinical research and want to make a difference, this is the job for you!

Overview:

A Clinical Research Associate (CRA) is a healthcare professional who works in clinical research and is responsible for monitoring the progress of clinical trials. The CRA is responsible for ensuring that clinical trials are conducted in accordance with the protocol, applicable regulations, and ethical standards.

Detailed Job Description:

A Clinical Research Associate is responsible for the planning, coordination, and execution of clinical trials. This includes the development of study protocols, the selection of clinical sites, the recruitment of study participants, the collection and analysis of data, and the reporting of results. The CRA is also responsible for ensuring that the clinical trial is conducted in accordance with the protocol, applicable regulations, and ethical standards.

What is Clinical Research Associate Job Skills Required?

• Knowledge of clinical research principles, regulations, and guidelines
• Excellent organizational and communication skills
• Ability to work independently and as part of a team
• Ability to manage multiple tasks and prioritize work
• Attention to detail and accuracy
• Proficiency in Microsoft Office applications

What is Clinical Research Associate Job Qualifications?

• Bachelor’s degree in a related field
• Previous experience in clinical research or related field
• Certification as a Clinical Research Associate (CCRA) or Clinical Research Professional (CRCP)

What is Clinical Research Associate Job Knowledge?

• Knowledge of clinical research principles, regulations, and guidelines
• Knowledge of Good Clinical Practice (GCP)
• Knowledge of medical terminology
• Knowledge of clinical trial design and data analysis

What is Clinical Research Associate Job Experience?

• Previous experience in clinical research or related field
• Experience in monitoring clinical trials
• Experience in data collection and analysis

What is Clinical Research Associate Job Responsibilities?

• Develop and implement clinical trial protocols
• Monitor clinical trial sites to ensure compliance with protocol and applicable regulations
• Recruit and screen study participants
• Collect and analyze data
• Prepare and submit reports to regulatory agencies
• Maintain accurate and up-to-date records
• Ensure the safety of study participants