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Clinical Project Specialist Jobs in New Jersey

Clinical Project Associate Jobs
By Canfield Scientific At Parsippany, NJ, United States
Strong time management, problem-solving, and organizational skills
Provide project management and operational support to designated clinical project team ensuring that quality, timelines, and project specifications are met
Manage study documentation ensuring accuracy within the documentation while aiding in the preparation of supply shipments to study sites
Associate degree or at least 1 year work experience
Medical device/medical terminology and photography experience is advantageous
HIPPA/GCP guidelines knowledge is a plus
Clinical Project Director I
By TekWissen ® At East Hanover, NJ, United States
Drives functional excellence in education, implementation and compliance to best practices and shares lessons learned for trial management.
An onboarding partner in case of no prior people management experience.
Strong project management skills and demonstrated ability to meet timelines.
an onboarding partner in case of no prior people management experience.
Drives the implementation, maintenance and resolution of clinical trial quality risk management process within the CTT.
Leads development of clinical outsourcing specifications and management of interface with Contract Research Organization.
Director, Clinical Project Lead
By Genmab At Princeton, NJ, United States
Experience with operational management and budget planning
Ensure close and transparent communication between the CDT and the Clinical Management Team (CMT)
Minimum requirement of 12 or more years of experience in clinical operations
Significant experience in leading and managing complex clinical projects/programs
Significant experience managing/guiding internal (cross-functional) and external (CRO, regulatory authorities) teams
Global clinical program level experience required
Clinical Specialist Jobs
By Outset Medical, Inc. At Greater Minneapolis-St. Paul Area, United States
Outset also offers the following benefits:
Effectively work cross-functionally with Outset Team members to deliver an exceptional customer experience.
Manage administrative tasks; reporting of dialysis treatments, training information and treatment growth outcomes in assigned region.
2 years of clinical experience, ideally in Dialysis
2 years medical device, biotech or pharmaceutical experience preferred
Excellent interpersonal skills with the ability to persuade decision makers
Project Specialist Jobs
By ZTransform At Greater Seattle Area, United States

ZTransform is growing! I am seeking talented systems engineers, project managers, workflow specialists, and several other technical operations savvy team members. Welcoming full-time and project-based ...

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