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Clinical Project Specialist Jobs in Arkansas

Clinical Project Coordinator Jobs
By PCM TRIALS - Quality Mobile Research At United States
Manage Certified Mobile Research Nurse certifications.
Contribute to initiatives for continual improvement of clinician management and onboarding.
Perform additional duties and responsibilities as necessary.
Previous work experience in a clinical or research setting is preferred.
Excellent verbal and written communication skills.
Identify nurses from an established nurse database to cover study visits as directed by each project execution team.
Clinical Project Assistant - Internship
By DICE Therapeutics At United States
Completes a variety of other clinical trial and project management-related responsibilities as assigned and agreed upon with direct manager
Uses time efficiently, completes tasks correctly and on time, follows instructions and responds to management direction
Coordinates and assists with team finance meetings
Previous clinical experience a plus; basic understanding of clinical trial processes is required
Strong attention to detail and excellent communication and organizational skills
Strong computer skills required including MS Office (Word, PowerPoint, MS Project), including a high-level proficiency /expertise in Excel
Clinical Project Associate - Wfh
By Sarah Cannon At United States
You will assist with confirming the qualifications of investigators and investigative sites throughout the conduct of the clinical trial
You will set-up, document collection/upload of files to the TMF/eTMF
You will perform initial quality review of documents prior to upload/filing in the TMF/eTMF
You review study documents to ensure they are current, complete and accurate
It’s More Than a Career, It’s a Mission.
About Sarah Cannon Research Institute

Are you looking for an exciting opportunity to join a dynamic team in a fast-paced environment? We are seeking a Clinical Project Specialist to join our team and help us develop and execute clinical trials. You will be responsible for managing the day-to-day operations of clinical trials, including protocol development, data management, and regulatory compliance. If you have a passion for clinical research and are looking for a challenging and rewarding career, this could be the perfect job for you!

Overview A Clinical Project Specialist is a professional who works in the field of clinical research and is responsible for managing clinical projects. They are responsible for the planning, coordination, and execution of clinical trials and studies. They ensure that the clinical trial is conducted in accordance with the protocol, applicable regulations, and good clinical practice (GCP). Detailed Job Description A Clinical Project Specialist is responsible for the planning, coordination, and execution of clinical trials and studies. They are responsible for developing and managing project timelines, budgets, and resources. They are also responsible for ensuring that the clinical trial is conducted in accordance with the protocol, applicable regulations, and good clinical practice (GCP). They are responsible for the coordination of all activities related to the clinical trial, including the recruitment of study participants, data collection, and data analysis. They are also responsible for the preparation of regulatory documents, such as informed consent forms and study protocols. Job Skills Required
• Knowledge of clinical research and clinical trial processes
• Knowledge of applicable regulations and good clinical practice (GCP)
• Excellent organizational and project management skills
• 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 applications
Job Qualifications
• Bachelor’s degree in a related field
• At least two years of experience in clinical research or clinical trials
• Certification in clinical research or clinical trials (preferred)
Job Knowledge
• Knowledge of clinical research and clinical trial processes
• Knowledge of applicable regulations and good clinical practice (GCP)
• Knowledge of data collection and analysis methods
• Knowledge of medical terminology
Job Experience
• At least two years of experience in clinical research or clinical trials
• Experience in project management
• Experience in data collection and analysis
Job Responsibilities
• Develop and manage project timelines, budgets, and resources
• Coordinate all activities related to the clinical trial, including the recruitment of study participants, data collection, and data analysis
• Prepare regulatory documents, such as informed consent forms and study protocols
• Monitor the progress of the clinical trial and ensure that it is conducted in accordance with the protocol, applicable regulations, and good clinical practice (GCP)
• Analyze and interpret data from the clinical trial
• Prepare reports and presentations on the results of the clinical trial