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Clinical Study Specialist Jobs

Clinical Study Manager - Ivd/Medtech - Remote
By NAMSA At United States
Act with integrity in everything we do.
Develop superior talent and deliver expertise.
Respond with agility and provide timely results.
Embrace collaboration, diverse perspectives and ideas.
Come and work for an organization with the:
Clinical Study Assistant Jobs
By Kelly Science, Engineering, Technology & Telecom At Irvine, CA, United States
Run reports including training matrix reports, metrics for management reviews
Support management of IRB/IEC renewal compliance.
Work with management group to help achieve department goals.
Requires experience and knowledge working with computer systems (Microsoft office –
Assist in payments/tracking for patient reimbursements. Performs data entry in systems
Is responsible for ensuring appropriate level of communication with managers, project leaders, and team members.
Clinical Specialist Jobs
By ImpactBio At Los Angeles Metropolitan Area, United States
Outstanding customer-focused and account management skills.
Become an expert at understanding the Healthcare Partner’s unmet needs related to the management and protection of closed surgical incisions.
Effectively communicate the clinical, ease-of-use and cost-savings benefits of NPseal® compared to traditional dressings and NPWT competitive offerings.
Develop and manage relationships with Key Customer decision-makers including Physicians, Nurses, decision makers, and Operating Room staff.
Manage travel and expenses per approved budget and timelines.
Other responsibilities as necessary to perform position.
Clinical Specialist Jobs
By ImpactBio At Greater Pittsburgh Region, United States
Act as the Clinical Expert in the field focusing on education, pull-through and workflow.
Experience in a sales or customer-facing role in Diagnostics, Life Sciences or the Medical Device Industry is required.
Experience working in a HIPAA and CLIA regulated environment preferred.
Excellent written and verbal communication skills.
Proficiency using a CRM system, Salesforce experience preferred.
Experience working in an environment with defined Service Level Agreements and Key Performance Indicators.
Clinical Specialist Jobs
By Abbott Neuromodulation At Chicago, IL, United States
Excellent organizational, time management and prioritizing skills.
EDUCATION AND EXPERIENCE YOU’LL BRING
Provides technical, clinical and programming assistance, primarily in support of 1-2 Territory Manager(s).
Assist Territory Managers in after hours call support and activities.
Works seamlessly with Territory Manager(s) allowing them increased selling time.
Will begin to conduct PCP work and educational in services, as directed.
Clinical Study Manager, Clinical Operations
By Daiichi Sankyo, Inc. At United States
Note that vendor management is not limited to the CRO, but includes ancillary vendors (e.g. translations, trial insurance, and central laboratory).
Ensure DS internal tracking systems are updated (e.g. Global Project Management System, GPMS).
Education Qualifications (from An Accredited College Or University)
Associate degree or with a nursing diploma with substantial experience preferred.
4 or More Years relevant experience is required with a BS preferred.
Bachelor's Degree in the Sciences preferred.
Clinical Study Nurse Coordinator
By University of Nebraska Medical Center At , Omaha $66,000 - $99,000 a year
Required Additional Knowledge, Skills and Abilities:
Preferred Additional Knowledge, Skills and Abilities:
If any experience is required, please specify what kind of experience:
If yes, what is the required licensure/certification?
Nursing experience in oncology and/or clinical research.
If yes, what is the preferred licensure/certification?:
Clinical Study Support - Icf
By ICON At , Remote
Bachelor’s Degree in business administration, finance, science or related field or equivalent experience.
Central Services Specialist - ICF Management
Co-manages maintenance of the centralized Informed Consent Form mailbox.
Minimum of three years of relevant experience in the biopharmaceutical/CRO industry.
Experience in negotiating vendor contracts/budgets.
Proven ability to effectively manage change.
Sr Clinical Study Coordinator- Full Time -Cancer,Clinical & Translational Research
By Henry Ford Health At , Detroit
Analyzes protocol specific requirements and implements quality assurance measures to ensure physician, patient, and clinician compliance.
Three (3) years of related experience required.
Organizational, analytical, and problem-solving skills required.
Demonstrated verbal and written skills at professional level required.
CERTIFICATIONS/LICENSURES REQUIRED: SOCRA or ACRP certification required.
education and training, the health system has trained nearly 40% of physicians currently practicing
Clinical Study Manager- Medical Devices
By Integrated Resources, Inc ( IRI ) At United States
Remote will be considered; however, Minnesota or central time zone will be preferred.
Familiarity with electrophysiology and/or cardiac arrhythmias is a plus.
Previous work history with CERs and EU MDRs
Previous work history in medical device or pharmaceutical research (i.e., no academia or research scientist candidate).
Previous work history in the cardiovascular space.
Minimum is BS + proven work history
Clinical Specialist, Cardiopulmonary Jobs
By LivaNova At Orlando, FL, United States
Perfusion education, Current or history of Clinical Certification or Licensure is required
Minimum Requirements And Qualifications (universal)
Develops and maintains product knowledge excellence of the LivaNova CP portfolio of products.
Develops and maintain an in-depth knowledge of assigned accounts and customers to include competitor activity.
Meet all requirements and maintain credentialing status in order to access accounts
Performs other related duties and responsibilities, on occasion, as assigned.
Clinical Specialist Jobs
By GS Medical USA At Irvine, CA, United States
• Experienced in data analysis and data insight skills
• Minimum of 4 years of professional experience or
• Strong interpersonal communication, influencing, critical thinking, and problem-solving skills required.
• Functional knowledge of human anatomy and physiology, basic knowledge of surgery
• Strong technical product knowledge of surgical instruments, procedures, protocols, and solutions preferred
• Provide Operating Room and Sterile Processing Department consultation.
Clinical Specialist (Wyoming) Jobs
By MedImpact Healthcare Systems At , Remote
Provides in-service education to PACs regarding topics such as PA guidelines, diagnoses commonly seen as part of the PA review process
This job has no supervisory responsibilities.
To perform this job successfully, an individual should have knowledge of Microsoft Office Suite Word Processing software.
Current, unrestricted Registered Pharmacist license in the United States as applicable to client requirement.
Responsible for providing clinical review support services to client plan(s) contracting for clinical services
This includes reviewing prior authorization requests and either deciding to approve or deny the request
Clinical Specialist - Minneapolis
By Relievant Medsystems, Inc. At Minneapolis, MN, United States
Strong organizational, planning, and time management
Acquires and maintains current knowledge of perioperative surgical technology practice and hospital policies and procedures
Develops technical acumen to a level to serve as an educational resource
Experience in minimally invasive spine procedures utilizing fluoroscopy, CT and MRI is essential.
Customer relationship and procedural skill development
High School Diploma or GED or Associate's Degree with a minimum 4 years of clinical or medical sales experience; or
Clinical Specialist Jobs
By Abbott At Pittsburgh, PA, United States
Provides insight, guidance, and feedback to management on market feedback and components of next generation of products.
Must apply engineering skills and abilities to interpret and solve complex clinical problems.
Assists Training and Education departments with advanced educational seminars, and the preparation of educational materials.
Performs related functions and responsibilities, on occasion, as assigned.
Bachelor’s degree in Bio-Medical Engineering, related field or equivalent healthcare experience required.
A minimum of two years increasingly responsible experience in the cardiac pacing and related industries.
Clinical Study Support- Icf
By ICON Strategic Solutions At United States
Co-manages maintenance of the centralized Informed Consent Form mailbox.
Minimum of three years of relevant experience in the biopharmaceutical/CRO industry.
Ability to manage multiple tasks simultaneously and meet deliverables in accordance with stated timelines.
MUST CURRENTLY WORK AT A CRO/PHARMA
Reviews and validates quality and accuracy of Informed Consent Form templates.
Supports development of Informed Consent Form templates.
Associate Director Clinical Study Management
By BeiGene At United States
Management experience of CROs, Vendors and Consultants preferred
Ensures the competencies and skills required for the Clinical team is consistent with the company defined requirements
Mentor junior team members to support development by delegating responsibilities, overseeing and supporting development plans
8+ years progressive experience in clinical operations preferably within the biotech, pharmaceutical, and/or CRO environment
Possess understanding of treatment landscape, standard of care, upcoming approvals, and good knowledge of KOLs and investigators
Experience developing trial plans including site monitoring, pharmacy and lab manuals, risk mitigation strategies, trial budgets and site selection/feasibility as required
Clinical Study Coordinator - Chatham, Ny
By Lightship At Chatham, NY, United States
Required knowledge, skills, and abilities
Supporting supply and inventory management, including:
Updating the inventory management system
Bachelor's Degree in Life Science or healthcare-related field, or requisite combination of education, training, and experience
Understanding and complying with all regulations, policies, and guidelines applicable to clinical research, including GCP, FDA, and IRB requirements
Collecting study data and completing data entry / case report forms in various electronic systems and on paper
Clinical Specialist Rvt - Louisville
By Boston Scientific At Louisville, KY, United States
Maintain current Customer Relationship Management (CRM) records
A working knowledge of GMP, ISO 13485 & MDD requirements.
Assist or act as Field Mentor when asked in the training and educational needs of incoming field personnel.
Facilitate the adoption of Varithena through education and awareness with RVTs
3-5 years of experience in a healthcare field
3-5 years of experience in the medical device industry as a clinical specialist or equivalent
Clinical Specialist Jobs
By Outset Medical, Inc. At New York City Metropolitan 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

Are you looking for an exciting opportunity to join a dynamic team of clinical research professionals? We are seeking a Clinical Study Specialist to join our team and help us advance our mission of improving patient care through clinical research. As a Clinical Study Specialist, you will be responsible for managing clinical studies, ensuring compliance with regulatory requirements, and providing support to clinical investigators. If you are passionate about clinical research and have the skills and experience necessary to succeed in this role, we want to hear from you!

Overview A Clinical Study Specialist is a healthcare professional who is responsible for the planning, implementation, and management of clinical studies. They work closely with clinical research teams to ensure that all aspects of the study are conducted in accordance with applicable regulations and protocols. Clinical Study Specialists are responsible for the coordination of all activities related to the study, including the recruitment of participants, data collection, and analysis. Detailed Job Description Clinical Study Specialists are responsible for the planning, implementation, and management of clinical studies. They work closely with clinical research teams to ensure that all aspects of the study are conducted in accordance with applicable regulations and protocols. Clinical Study Specialists are responsible for the coordination of all activities related to the study, including the recruitment of participants, data collection, and analysis. They are also responsible for the preparation of study documents, such as protocols, informed consent forms, and study reports. In addition, Clinical Study Specialists are responsible for the training of research staff, the monitoring of study progress, and the management of study budgets. Job Skills Required
• Knowledge of clinical research regulations and protocols
• Excellent organizational and communication skills
• Ability to work independently and as part of a team
• Ability to manage multiple tasks and prioritize effectively
• Proficiency in Microsoft Office Suite
• Knowledge of medical terminology
Job Qualifications
• Bachelor’s degree in a related field
• At least two years of experience in clinical research
• Certification in clinical research (e.g. CCRA, CCRP)
Job Knowledge
• Knowledge of clinical research regulations and protocols
• Knowledge of medical terminology
• Knowledge of data collection and analysis methods
• Knowledge of study design and implementation
Job Experience
• At least two years of experience in clinical research
• Experience in the preparation of study documents
• Experience in the training of research staff
• Experience in the monitoring of study progress
• Experience in the management of study budgets
Job Responsibilities
• Plan, implement, and manage clinical studies
• Ensure that all aspects of the study are conducted in accordance with applicable regulations and protocols
• Coordinate all activities related to the study, including the recruitment of participants, data collection, and analysis
• Prepare study documents, such as protocols, informed consent forms, and study reports
• Train research staff
• Monitor study progress
• Manage study budgets