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Clinical Project Specialist Jobs

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 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.
Clinical Project Associate - Wfh
By Sarah Cannon At Tennessee, United States
Assist with confirming the qualifications of investigators and investigative sites throughout the conduct of the clinical trial
Set-up, document collection/upload of files to the TMF/eTMF
Perform initial quality review of documents prior to upload/filing in the TMF/eTMF
Partner with document specialist to maintain the Trial Master File (TMF) in “audit ready” condition from study start to completion
Review study documents to ensure they are current, complete and accurate
It’s More Than a Career, It’s a Mission.
Clinical Project Director Jobs
By Allucent At Cary, NC, United States
Extensive clinical project management experience, with at least 5 years of clinical project management experience
Responsible for overall quality and management of the delivery clinical trial projects and programs
Manages complex, cross-functional resource requirements in line with budgeted, time, scope, and quality expectations for project delivery
Ensures effective risk management across the project delivery lifecycle
Expert knowledge of ICH-GCP(R2), data and patient privacy practices, and applicable (local) regulatory requirements
Strong general administrative skills and experience
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 Supplies Project Specialist
By Moderna At Cambridge, MA, United States
1 - 3 years of clinical drug supply management, clinical supply chain, clinical supplies, hospital pharmacy, pharmacy experience or equivalent required
IRT design and management experience preferred
Experience with Clinical Supply Inventory Management systems preferred
Prior Cold Chain packaging, labeling, distribution experience preferred
Proficiency with word processing, spreadsheet, database, presentation software (MS Office skills such as Outlook, Word, Excel, PowerPoint, and SharePoint)
Experience in maintaining relationships with vendors preferred
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 Coordinator - 122977
By UC San Diego Health At San Diego, CA, United States
Strong knowledge of investigational protocols (data management, query resolution, protocol design and protocol implementation). Working knowledge of medical and scientific terminology.
Experience performing clinical research duties in a clinical research environment such as CRO, academic research institution, and/or a research hospital.
Strong experience with research protocol in order to screen patients for eligibility, initiate treatment plan, collect specimens, and orient participating physicians.
Strong knowledge of experimental protocols, data gathering, protocol design and evaluation.
Strong experience in clinical trials research.
Experience completing clinical trials case report forms via hard copy and online.
Clinical Office Specialist / Cna
By Tanner Clinic At Layton, UT, United States
CNA certification or 1 year medical office experience required.
Electronic Medical Records experience helpful.
Excellent verbal and written communication skills.
Excellent keyboarding and computer skills.
Receive phone calls and respond to patient concerns.
Obtain prior authorizations for prescriptions and procedures.
Project Specialist Jobs
By SPECTRAFORCE At Austin, TX, United States
Vendor PO management and tracking
Looking for a replacement candidate with tenure experience that can come in and hit the ground running.
Manage fixture demand planning spreadsheets and process
Location: Austin TX, (Hybrid Remote)
Ability to work in a fast-paced environment
Maintain internal database by ensuring correct information is entered into the system
Clinical Project Manager Jobs
By X4 Life Sciences At North Carolina, United States
5 Years of Project Management
If you think you have the right skills and experience, please apply for immediate consideration!
Ability to manage and execute complex trials
5 Years Oncology experience, Phase 1 experience required
Some day-to-day responsibilities may include:
Provide strong, independent Clinical Operations leadership
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
Clinical Specialist Jobs
By Johnson & Johnson At California, United States
Manage area operations while providing exceptional customer service and experience.
Experience in nursing science, preferably in the operating room, would be a definite asset.
Develop new growth opportunities and exceed customer expectations with Ethicon products and solutions
Execution of national/regional/local promotional activities and programs for Ethicon products.
Contribute to Ethicon's success by providing information on market, customer and environmental changes.
Develop strong clinical relationships with our most influential clients
Project Specialist Epmo Jobs
By Wellstar Health System At Marietta, GA, United States
Experience with project management and process improvement methodologies Required
Support the administrative and tactical management of projects from beginning to end through all administrative processes and tools available
In coordination with EPMO Manager, estimate resources and participants needed to achieve project goals, including management of vendors or consultant resources
Facilitate policies and procedures during the project needed to meet deliverables (contract facilitation/management)
Attend management, project team, and customer meetings as requested
Bachelor's Degree in Business or Healthcare Management Required or
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 ...

Specialist (Clinical Biologics) Jobs
By AstraZeneca At Gaithersburg, MD, United States
Serves as the “Subject Matter Expert” in unit operations to improve quality, ensure safety, and drive process efficiency and accuracy
Support process improvement initiatives and authors or revises standard operating procedures accordingly.
Monitors process parameters, contributes to investigations, troubleshoots during processing, and recommends potential solutions.
Reviews executed Production Records for accuracy and completion
Ability to use MS Office tools and AstraZeneca enterprise systems
Ability to work with others in a team environment and lead a team of peers
Project Specialist Jobs
By Monster Energy At Corona, CA, United States
Bachelor’s Degree preferred, applicable training certification, or equivalent work experience
Coordinating with cross discipline team members to make sure that all parties are on track with task requirements, deadlines, and schedules
Excellent interpersonal, written, and verbal communication skills
Strong computer skills and proficiency with Microsoft Office programs (Outlook, Excel, Word, Visio, etc.)
Coordination of task details, planning and execution
Coordinate meetings with internal and external project/tasks team members to identify and solve problems
Project Specialist Jobs
By CampusPoint At Seattle, WA, United States
Experience in project management and contract management strongly preferred
Working knowledge of Salesforce and Google Ad Manager strongly preferred
Assist Account Managers in confirming availability of underwriting and digital advertising inventory
Notify Sales Manager, Traffic Department, Accounting Department & Corporate Development Account Managers when make-goods are required
Experience with multi-platform marketing and advertising strongly preferred
Working knowledge of MS Office (Word and Excel) required

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