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Clinical Research Coord Associate 220679 Jobs

Coord,Clinical Research Ii - 100% Remote
By Talentify.io At United States
Track and maintain study-related information in the data management system
Ensure adherence to study protocols and regulatory requirements
Bachelor's degree in a scientific or health-related field, or equivalent experience
1-3 years of related experience
Obtain consent of research participants in accordance with IRB approved protocols and regulations, including HIPAA
Schedule and conduct participant study visits, tests, interviews, and telephone follow-up calls
Clinical/Translational Research Coord I
By Vanderbilt University Medical Center At Nashville, TN, United States
Communicates a basic knowledge and understanding of the management and implementation of clinical/translational research operations
Procures equipment and supplies needed to fulfill project requirements
Participates in the determination of eligible candidates for study participation, assuring participants fulfill eligibility requirements
With supervision, develops and manages study budgets, monitoring efficient invoicing and taking appropriate action to maintain clinical trial billing compliance
Participates in and maintains certifications, licensure and credentialing as required by Vanderbilt, the department and Sponsor
Furthers knowledge base by attending a Basic Research 101 within first three months of employment date
Clin/Tran Research Coord Ii
By Vanderbilt University Medical Center At Nashville, TN, United States
Identifies and procures equipment and supplies needed to fulfill project requirements (locally and across multiple sites, if required)
The responsibilities listed are a general overview of the position and additional duties may be assigned.
Communication (Novice): Clearly, effectively and respectfully communicates to employees or customers.
Discover Vanderbilt University Medical Center:
Aligning with Vanderbilt Health’s Strategic Directions
Clinical Program Coord Jobs
By One Call At Jacksonville, FL, United States
Excellent time management skills with a proven ability to meet deadlines.
General Knowledge, Skills & Abilities
Associate’s degree is required; Bachelor’s degree is preferable; or the equivalent combination of education, training, and work experience.
Opportunities to work from home
Tuition Reimbursement Program including certifications
Communicates Gold Standard Review™ results to Adjuster and/or Case Manager, including any outstanding provider or reviewer requests for information.
Research Program Coord I
By Mount Sinai Health System At New York, NY, United States
Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.
Prior experience in clinical research and IRB protocol preparation will be preferred, but not required.
Excellent written and oral communication skills.
Collects and records study data. Inputs all information into database.
Secures, delivers and ships clinical specimens as required by the protocol.
Exhibits the results of the research studies to groups of people.
Research & Admin Coord In One Welfare & Sustainability
By The Ohio State University At , Columbus, 43210, Oh $32,025 - $42,675 a year
The targeted hiring range for this position is $32,025 - $42,675 annually, commensurate with education and experience
Excellent oral and written communication skills, ability to work cooperatively with faculty, staff, and external stakeholders
Experience managing administrative tasks associated with research and outreach
excellent oral and written communication skills, ability to work cooperatively with faculty, staff, and external stakeholders
experience managing administrative tasks associated with research and outreach
Advanced training (e.g. MS or a PhD) in a field relevant to the welfare of animals

Are you looking for an exciting opportunity to join a dynamic team of clinical research professionals? We are seeking a Clinical Research Coord Associate to join our team and help us make a difference in the lives of patients. This position offers a competitive salary and benefits package, and the chance to work with cutting-edge technology and innovative research. If you have a passion for clinical research and are looking for a rewarding career, this could be the perfect job for you!

Overview:

The Clinical Research Coord Associate 220679 is responsible for providing administrative and operational support to clinical research projects. This position requires excellent organizational and communication skills, as well as the ability to work independently and as part of a team.

Detailed Job Description:

The Clinical Research Coord Associate 220679 is responsible for providing administrative and operational support to clinical research projects. This includes developing and maintaining project timelines, coordinating meetings and conference calls, preparing and submitting regulatory documents, and managing project budgets. The Clinical Research Coord Associate will also be responsible for tracking and reporting project progress, and providing support to the research team.

What is Clinical Research Coord Associate 220679 Job Skills Required?

• Excellent organizational and communication skills
• Ability to work independently and as part of a team
• Knowledge of clinical research protocols and regulations
• Proficiency in Microsoft Office applications
• Ability to manage multiple projects simultaneously
• Attention to detail

What is Clinical Research Coord Associate 220679 Job Qualifications?

• Bachelor’s degree in a related field
• At least two years of experience in clinical research
• Knowledge of clinical research protocols and regulations
• Proficiency in Microsoft Office applications

What is Clinical Research Coord Associate 220679 Job Knowledge?

• Knowledge of clinical research protocols and regulations
• Knowledge of Good Clinical Practice (GCP)
• Knowledge of clinical trial design and methodology
• Knowledge of medical terminology

What is Clinical Research Coord Associate 220679 Job Experience?

• At least two years of experience in clinical research
• Experience in project management
• Experience in data management
• Experience in regulatory document preparation

What is Clinical Research Coord Associate 220679 Job Responsibilities?

• Develop and maintain project timelines
• Coordinate meetings and conference calls
• Prepare and submit regulatory documents
• Manage project budgets
• Track and report project progress
• Provide support to the research team