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Clinical Trial Researcher Jobs in Arkansas

Remote - Senior Clinical Trial Specialist
By Beacon Hill Staffing Group At United States
5+ years previous clinical research experience in clinical trial coordination, site management, and or vendor management.
Must have the ability to build and maintain positive relationships with management and peers
Manage the collection, review and approval of regulatory documents from clinical sites
Manages and tracks study specific payments
Manage ancillary vendors, such as a specialty lab
Review site visit reports, under the direction of the Clinical Program Manager or designee
Clinical Trial Monitor Jobs
By Medasource At United States
Monitor clinical trial progress through a combination of remote data review and on site monitoring visits. Some travel will be required.
3+ years of progressively responsible clinical trials experience with 2+ years of monitoring experience.
Assist in the development and writing of clinical trial monitoring plans.
Provide recommendations and guidance to study specific monitoring teams and assist in audit readiness and preparation.
Participate in regular monitoring team group meetings.
Bachelor's degree in a field relevant to research compliance
Clinical Trial Assistant Jobs
By Advanced Recruiting Partners At United States

Support for Study Start-up and Close-out: Contribute to study start-up and close-out activities, including site initiation, investigator meetings, and archiving processes.

Clinical Trial Monitoring Specialist
By Infosoft, Inc. At United States
3-5 years of experience required
Experience with medical device monitoring is required.
Experience with cardiac trials and/or blinded trials is preferred.
Experience with Medidata RAVE and Medidata CTMS is preferred.
Remote with frequent travel to clinical sites (Pacific or Mountain Time Zone)
remote and onsite monitoring activities
Clinical Trial Supply Chain Specialist
By Mindlance At United States
SAP software based computer systems experience.
MS Office and MS Teams experience.
SKYPE Meeting or Virtual Meeting software experience.
GMP and Pharmaceutical Industry Regulations knowledge.
Ability to learn multiple computer systems.
Clinical Trial Liaison Jobs
By Mirum Pharmaceuticals, Inc. At United States
Clinical site management experience, with an understanding of the operational aspects of clinical research and clinical development outsourcing
Excellent written and verbal communication skills - able to interact with all levels of internal and external management
Self-motivated with proactive issue monitoring and management including risk assessment and contingency planning
Other tactical or strategic requirements in line with the study team
5 years’ experience in clinical research in Pharma, Biotech or CRO or related experience
Demonstrated experience of working directly with clinical sites and investigators
Sr Consultant, Clinical Trial Compliance, Audit, & Inspection Readiness
By EG Life Sciences At United States
5+ years of Global Pharmaceutical Clinical Study Management:
1) 10+ years of Clinical Research Experience:
Audit & Inspection Readiness Experience:
ADDITIONAL QUALIFICATIONS / NICE TO HAVES
1) GCP and Clinical Quality experience
Sr Consultant, Clinical Trial Compliance, Audit, & Inspection Readiness
Clinical Trial Project Manager
By SRG At United States
3 years of relevant clinical research and project management experience with a CRO, pharmaceutical, biotechnology / device company
Strong project management skills including client management, fiscal / contract management, and quality management
Perform contract and financial management activities for assigned trials and serve as central point of contact with sponsor for project updates
Oversee all aspects of clinical research projects to assure applicable regulations, standard operating procedures, and sponsor requirements are met.
Bachelor’s Degree or equivalent experience
Good knowledge of FDA guidelines and review processes, IND and NDA processes, and GCPs
Clinical Trial Coordinator - Monitoring (Remote)
By Merck At United States
Effective time management, organizational and interpersonal skills, conflict management
Clinical supply & non-clinical supply management, in collaboration with other country roles
Manage Labeling requirements and coordinate/sign translation change request, in collaboration with other country roles (if applicable)
Ensure proper provisioning for Learning Management System (CLMS) for all study site staff.
Credit Management within Learning Management System
Excellent negotiation skills for CTCs in finance area
Clinical Trial Manager Jobs
By Advanced Recruiting Partners At United States
· Maintains compliance in assigned region or project for performance, deliverables, and associated KPI’s.
· Ensures alignment of clinical activities to budget, including identification of out of scope activities.
· May participate in business development proposals, defense meetings and proposal development.
Clinical Trial Specialist Jobs
By Hawthorne Effect, Inc. At United States
Strong organization skills with experience with balancing priorities and resources.
Visit Management: Support logistics and visit scheduling teams by communicating relevant study information to Clinical Success team
Clinical Trial Experience is highly preferred but not required.
Strong skills in the use of technology, tools, operating systems, and software and is comfortable using these daily.
A creative and resourceful problem-solver with strong critical thinking skills.
GCP and good documentation practice expertise is required
Clinical Trial Assistant / Trial Documentation (Tmf)
By Apex Systems At United States
1. Provide start-up and ongoing trial regulatory document management
5. Setup and manage regulatory document trackers/reports as assigned.
6. Maintain a professional approach respecting the dignity and confidentiality of associates, manager, and vendors.
11. Maintain CEUs for SOCRA or ACRP certification.
• Oncology experience preferred. Prior experience managing flow of clinical trial regulatory documents preferred
4. Ensure quality product deliverables at all times.
Clinical Trial Manager Jobs
By Astrix At United States
Strong project management and team leadership capability
Leads local trial team to ensure integrity of trial conduct, assurance of patient safety, in line with regulatory requirements
Leads the local trial team as an OPU Clinical Trial Manager (CTM) Trial Preparation, Conduct and Closeout
B.S., M.S., or PhD plus a minimum of 3 years of experience in clinical research in pharmaceutical industry
Knowledgeable across all aspects of clinical trial operations and execution.
In collaboration with Site Monitoring Lead and CRAs, ensure Trial contact for CRAs, investigators and site staff.
Clinical Trial Document Management (Ctdm) Specialist
By Alcon At United States
Enter and maintain site information and document tracking in current clinical trial management systems.
Travel Requirements: minimal to no travel if located in Fort Worth; less than 10% if remote
Bachelor’s Degree or Equivalent years of directly related experience (or high school +8 yrs; Assoc.+4 yrs)
Basic knowledge of clinical trial processes
Alcon provides a robust benefits package including health, life, retirement, flexible time off, and much more!
Benefit from working in a highly collaborative and diverse environment, as well as within a welcoming and empowered team.
Senior Clinical Trial Manager
By Tourmaline Bio At United States
Strong working knowledge of cGCP/ ICH guidelines, and US and international clinical regulatory requirements
Develop and manage clinical trial budget and facilitate contract review
Adhere to relevant company policies and SOPs, cGCP/ICH guidelines, QC/QA procedures, as well as relevant clinical regulatory requirements
Advanced degree or certification is a plus
5+ years of clinical trial operations experience in a biotech, pharmaceutical, CRO, clinical research site or related healthcare company
Experience working on a multi-phase clinical program is a plus
Global Clinical Trial Associate
By ICON Strategic Solutions At United States
Benefits of Working in ICON:
Organizes Study Team meetings and prepares meeting minutes
Assists with organizing Investigator Meetings
Assists with preparation and review of study documents
Ships study documents and supplies to investigational sites and tracks delivery
Submits study documentation to Trial Master File
Clinical Trial Manager Jobs
By Technical Resources International, Inc. At Washington DC-Baltimore Area, United States
Demonstrated task management skills, with senior team member oversight.
Ensures project quality and compliance with FDA regulations and ICH (R2) guideline, and with NIH policies or other sponsors-specific requirements.
Strong presentation, problem-solving, and conflict resolution skills.
Seasoned oral and written communication skills.
Drives innovative project and company performance improvement solutions and sharing of best practices, including corrective and preventive (CAPA) actions, as needed.
Contributes to Business Development and Corporate Initiatives, e.g., SOP development and proposals for government and commercial clients.
Clinical Trial Associate - Remote
By Atlas Search At United States
Support Clinical Project Management team in communication to CRO, Vendors and Investigator Sites.
Assist Clinical Project Management team in the collection, review and filing of site Essential Documents, and maintenance of the TMF.
Minimum of 2+ years of industry experience
Participate in regular team meeting / teleconferences; CRO, Vendor and Investigator Site meetings as necessary; and Investigator Meetings, as necessary.
Bachelor’s Degree in health science or related field
Ability to travel as required.
Clinical Trial Supplies Manager
By Mindlance At United States
• Proficient and strong Project management skills.
• Moderate / Strong knowledge of the global drug development process and global regulatory requirements.
• Proficient knowledge of import / export requirements.
• An equivalent combination of education and experience may substitute.
• Demonstrating strong knowledge when presenting clinical supply processes at cross-functional meetings and actively participates.
• Ability to coach new Trial Supply Managers on individual tasks.
Clinical Trial Lead Jobs
By Avania At United States
Ability to work concurrently on multiple protocols and procedures; organizational, time management skills and problem-solving abilities
RN or BA/BS degree in a science/life science, engineering or health-related field plus a minimum 4 years monitoring experience
Experience as mentor and trainer for new CRAs
Excellent communication skills; demonstrated professional writing proficiency
Experience generating project-specific training presentations and coordinating necessary training
Ability to generate monitoring tools; experience generating and giving professional presentations

Are you looking for an exciting opportunity to make a real difference in the world of clinical research? We are seeking a Clinical Trial Researcher to join our team and help us develop innovative treatments for patients. As a Clinical Trial Researcher, you will be responsible for designing and executing clinical trials, analyzing data, and reporting results. You will have the opportunity to work with leading medical professionals and be part of a team that is making a real impact in the medical field. If you are passionate about clinical research and want to make a difference, this is the job for you!

Overview:

Clinical Trial Researchers are responsible for the design, implementation, and analysis of clinical trials. They work with medical professionals to ensure that the trials are conducted in accordance with the highest standards of safety and efficacy. They also collaborate with other researchers to ensure that the data collected is accurate and reliable.

Detailed Job Description:

Clinical Trial Researchers are responsible for designing, implementing, and analyzing clinical trials. They work with medical professionals to ensure that the trials are conducted in accordance with the highest standards of safety and efficacy. They also collaborate with other researchers to ensure that the data collected is accurate and reliable. They must be able to interpret and analyze the data collected from the trials and present their findings in a clear and concise manner. They must also be able to communicate effectively with medical professionals, other researchers, and sponsors of the trials.

What is Clinical Trial Researcher Job Skills Required?

• Knowledge of clinical trial design and implementation
• Knowledge of medical terminology and clinical trial protocols
• Ability to interpret and analyze data
• Excellent communication and interpersonal skills
• Ability to work independently and as part of a team
• Ability to work under pressure and meet deadlines
• Proficiency in Microsoft Office Suite

What is Clinical Trial Researcher Job Qualifications?

• Bachelor’s degree in a related field such as biology, chemistry, or public health
• Master’s degree in a related field such as clinical research, epidemiology, or biostatistics
• Certification in clinical research (CCRP)
• Experience in clinical research or related field

What is Clinical Trial Researcher Job Knowledge?

• Knowledge of clinical trial design and implementation
• Knowledge of medical terminology and clinical trial protocols
• Knowledge of data analysis and interpretation
• Knowledge of regulatory requirements for clinical trials

What is Clinical Trial Researcher Job Experience?

• Previous experience in clinical research or related field
• Experience in data analysis and interpretation
• Experience in clinical trial design and implementation

What is Clinical Trial Researcher Job Responsibilities?

• Design and implement clinical trials in accordance with the highest standards of safety and efficacy
• Collaborate with medical professionals and other researchers to ensure accuracy and reliability of data collected
• Interpret and analyze data collected from the trials
• Present findings in a clear and concise manner
• Communicate effectively with medical professionals, other researchers, and sponsors of the trials
• Ensure compliance with regulatory requirements for clinical trials