Register
Recruit Create CV

Apex Clinical Research Associate Jobs in Union, Arkansas

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 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
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
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
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
Lead Clinical Research Associate
By Tourmaline Bio At United States
Assist the Senior Clinical Trial Manager in the review of Informed Consent Forms and other essential study documents
Certification as a Clinical Research Associate or Clinical Research Professional is highly desirable
3+ years clinical trial site monitoring experience in a biotech, pharmaceutical and/ or CRO company
Good understanding and working knowledge of clinical research and phases of clinical trials
Strong written and oral communication skills
Knowledgeable of Electronic Data Capture and other IT systems (CTMS, Microsoft Office, etc.)
Clinical Research Associate Trainee - Future Cra Academy
By Worldwide Clinical Trials At United States
Excellent planning and organizational skills with effective time management
Ability to work in a fast-paced environment and to comply with regulatory requirements and deadlines
1 year of experience working in Clinical Research required
Fluent in the local languages of the countries under responsibilities and proficient in both spoken and written English
Document site visit findings via written reports
Assess, monitor, and train study site staff on protocol adherence as required
Associate Director Clinical Research
By MSI Pharma At United States
We are looking for professionals with these required skills to achieve our goals:
• Experience in the clinical development/drug development/OTC Drug development process.
• Experience in the Pharmaceutical or healthcare industry. Consumer Health care experience is greatly preferred.
• Experience in regulatory / health authority interactions on clinical designs/submissions.
• Experience within Pain relief or OTC Drugs
• Demonstrated experience representing an organization with external stakeholders.
Clinical Research Associate (Medical Device)
By Rangam At United States
Responsible for implementing the stategic initiatives established by the business and the department.
Responsible for tactical components of creating and driving customer-centric relationships cross-functionally to support product developments throughout the product(s) life cycle.
Subject matter expert (SME) in the technical application of product portfolio.
Travel up to 30% of the time domestically and / or internationally.
Responsible for the execution of all aspects of clinical studies including but not limited to:

Are you looking for an exciting opportunity to join a dynamic team of clinical research professionals? Apex Clinical Research is looking for a Clinical Research Associate to join our team and help us make a difference in the lives of patients. As a Clinical Research Associate, you will be responsible for managing clinical trials, ensuring compliance with regulatory requirements, and providing support to clinical teams. If you have a passion for clinical research and want to make a difference, this is the job for you!

Overview Apex Clinical Research Associates are responsible for conducting clinical research studies in a variety of settings. They are responsible for collecting and analyzing data, preparing reports, and presenting findings to stakeholders. They must be knowledgeable in clinical research protocols and regulations, and must be able to work independently and collaboratively with other members of the research team. Detailed Job Description Apex Clinical Research Associates are responsible for conducting clinical research studies in a variety of settings. They are responsible for designing and implementing research protocols, collecting and analyzing data, preparing reports, and presenting findings to stakeholders. They must be knowledgeable in clinical research protocols and regulations, and must be able to work independently and collaboratively with other members of the research team. They must also be able to communicate effectively with research participants and other stakeholders. Job Skills Required
• Knowledge of clinical research protocols and regulations
• Ability to design and implement research protocols
• Ability to collect and analyze data
• Ability to prepare reports and present findings
• Ability to work independently and collaboratively
• Excellent communication and interpersonal skills
Job Qualifications
• Bachelor’s degree in a related field
• Previous experience in clinical research
• Knowledge of clinical research protocols and regulations
• Ability to design and implement research protocols
• Ability to collect and analyze data
• Ability to prepare reports and present findings
• Ability to work independently and collaboratively
• Excellent communication and interpersonal skills
Job Knowledge Apex Clinical Research Associates must have a comprehensive understanding of clinical research protocols and regulations. They must be knowledgeable in the design and implementation of research protocols, data collection and analysis, and report preparation and presentation. Job Experience Apex Clinical Research Associates must have previous experience in clinical research. They must be able to work independently and collaboratively with other members of the research team. Job Responsibilities
• Design and implement research protocols
• Collect and analyze data
• Prepare reports and present findings
• Communicate effectively with research participants and other stakeholders
• Ensure compliance with clinical research protocols and regulations
• Work independently and collaboratively with other members of the research team