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Clinical Project Specialist Jobs

Clinical Specialist - Southern California
By Vertos Medical At , Irvine, Ca $80,000 - $90,000 a year
Experience in pain management, spinal surgery, or related specialties.
Operating room procedural knowledge, etiquette, and experience.
Relevant industry, healthcare, marketing, or medical education experience where there is specific focus on clinical case support and education.
High level of organization and prioritization regarding schedule management and follow-up.
Ability to interact cross-functionally and proactively escalate issues with integrity to appropriate levels of management in the organization.
Positive attitude and passion for working within the pain management and anesthesiology field.
Clinical Project Manager Jobs
By Albion Rye Associates At Boston, MA, United States
Preferably two or more years of project management experience.
Bachelor’s degree in biological science or other related field and/or a combination of education and experience.
Builds the electronic Trial Master File (eTMF) for the project; oversees and manages the collection and filing of essential trial documents.
Clinical Project Manager $105,000 - $135,000 year
Preferred 2 years experience as a CPM
Experience monitoring or overseeing clinical trial sites are required.
Clinical Specialist - Orlando, Fl
By Vertos Medical At , Orlando, Fl $80,000 - $90,000 a year
Experience in pain management, spinal surgery, or related specialties.
Operating room procedural knowledge, etiquette, and experience.
Relevant industry, healthcare, marketing, or medical education experience where there is specific focus on clinical case support and education.
High level of organization and prioritization regarding schedule management and follow-up.
Ability to interact cross-functionally and proactively escalate issues with integrity to appropriate levels of management in the organization.
Positive attitude and passion for working within the pain management and anesthesiology field.
Clinical Specialist/Bcba Jobs
By Journey Found At , Manchester, 06042, Ct
The Clinician’s Knowledge, Skills, Abilities & Responsibilities:
BCBA | Experience with Electronic Health Record Software
Our Next Clinical Specialist has these Characteristics:
These Competencies are Helpful & Preferred:
Project Specialist Jobs
By IRIS USA, Inc. At Greater Phoenix Area, United States

Responsibilities • SUMMARY: Coordinates, supervises, conceptualizes, designs, implements, tests, documents, and supports new and existing software and systems • Takes an active role in problem solving ...

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