Senior Clinical Development Specialist Job at Adtalem Global Education (Atlanta)

Senior Clinical Application Specialist

Looking for an exciting challenge? A change in pace using your Rad Tech skill to...

Location

Egypt , Cairo

Salary:

Not provided

PaxeraHealth

Expiration Date

Until further notice

Requirements

Excellent English Language
Experience as a radiology technologist or in similar clinical role
A deep understanding of medical imaging and the challenges faced by professionals in this industry
A Bachelor’s degree in Radiology, Biomedical Engineering or similar field
Strong presentation skills with sales ability
Ability to absorb and convey highly technical information
A hands-on and customer-centric approach
Must be able to travel to demonstrate to clients and to trade shows on occasion
Good time management skills and ability to prioritize tasks
Ability to work as part of a team

Job Responsibility

Serve as a software expert to clients and internal team members
Conduct webinars and workshops to demonstrate and provide technical expertise, support and training to clients as it relates to PaxeraHealth applications remotely and on-site
Create presentations, videos and other training materials as required for webinars, workshops and training sessions
Interfaces between clients/potential clients and company development team, skillfully forwarding pertinent suggestions and ideas to development for inclusion in future enhancements of software
Participate in the product development process
Develop and manage software documentation and technical support content including user manuals video-based tutorials and training tools
Attend conferences and exhibitions, meet with clients and demonstrate PaxeraHealth medical imaging solutions
Help with the product setup process as well as provide product presentations to customers and visitors during trade shows
Work together with technical teams and user groups to solve clients’ problems with available technology including hardware, software, databases and peripherals

Fulltime

Senior Specialist Education

Senior Specialist Education who excels in this role collaborates with nurse mana...

Location

United States , Martinsville

Salary:

Not provided

Copper Springs East

Expiration Date

Until further notice

Requirements

Current VA RN (or compact state) License
Graduate of a professional school of Nursing
Master's degree or currently enrolled in Master's in Nursing program required
Basic Life Support certification is required
Minimum two (2) years of clinical experience in an acute care hospital setting required
One (1) year of formal/informal teaching experience preferred
One (1) year of management experience preferred

Job Responsibility

Collaborates with nurse managers and staff to assess the learning needs and competencies of staff
Designs, delivers, and assesses learning activities and curriculums related to clinical competencies, departmental/organizational policies, regulatory requirements, and the use of clinical information technologies
Serves as a consultant/mentor for staff in areas of program development, clinical practice, and professional development
Participates in the development, coordination, and delivery of new staff orientation and education activities
Assists in development and implementation of educational programs/learning aids for clinical and non-clinical associates
Plans, coordinates, organizes, implements, and evaluates orientation programs, continuing education, and in-services that enhance associate job performance
Keeps appropriate educational records
Maintains A-V equipment, books, and educational supplies
Prepares schedules as needed for educational in-services and coordinates with persons involved
Conducts and assists others in orientation, in-services, continuing education, or workshops

What we offer

Multiple levels of medical, dental and vision coverage
Medical plans starting at just $10 per pay period
Tailored benefit options for part-time and PRN employees
Life, accident, critical illness, hospital indemnity insurance
Short- and long-term disability
Paid family leave
Paid time off
Higher education and certification tuition assistance
Loan assistance
401(k) retirement package and company match

Fulltime

Clinical Development Nurse

As a Divisional Clinical Development Nurse (RGN) at Barchester, you’ll lead, sup...

Location

United Kingdom , Hull

Salary:

60000.00 GBP / Year

Barchester Healthcare

Expiration Date

January 19, 2026

Requirements

Registered Nurse (RGN) with a current NMC registration
Evidence of continued professional development
Strong understanding of current regulatory requirements
Experience working in a Mental Health Hospital environment
Confident clinical mentor, including with newly-qualified nurses
Leadership skills
Sharp analytical mind
Ability to share knowledge, build relationships, and deliver on action plans
Willingness for regular travel

Job Responsibility

Lead, support and continuously improve the clinical governance and quality of care for patients in six Mental Health Hospitals across England
Support the performance of each hospital ensuring it performs to the highest clinical standards
Review the clinical governance database and KPIs of each home every month
Analyse results and identify practical strategies to ensure all regulations are met and care is continually improved
Work closely with the Director, improvement specialists and senior clinical staff in each service
Support the continual improvement of standards and help implement key actions to address any issues
Organise new training
Help attract key senior clinical staff
Deliver clinical investigations

What we offer

Company car or car allowance, mobile phone and laptop
Annual bonus
A range of holiday, retail and leisure discounts
Learning and development opportunities

Fulltime

Senior Study Specialist, Global Study Operations

The Sr. Study Specialist (SS) significantly contributes to or leads tasks relate...

Location

United Kingdom , London

Salary:

Not provided

BioMarin Pharmaceutical

Expiration Date

Until further notice

Requirements

BA/BS or higher in nursing, life or health sciences is preferred
Industry or relevant experience in lieu of education is considered
Experience in a biotechnology or pharmaceutical company
Experience in oversight of external vendors including SOW, budgets, POs, and invoice management (e.g., CROs, central labs, imaging etc.)
Proficient knowledge and experience in Agility and Proactivity, Leadership, Communication and Collaboration, Study Management and Execution, Compliance and Quality, Drug Development and Study Design, Product and Therapeutic Area Knowledge

Job Responsibility

Develop study specific documentation, as delegated by the Study Manager
Contribute to the oversight of country and site feasibility assessment and site selection
Oversight of CRO for IRB/EC related submission/approval activities
Oversight of essential documents for study life-cycle management
Develop/Oversee site and investigator training materials
Present at investigator meetings as assigned
Ensure accurate and timely study entry and updates to ClinicalTrials.gov
Facilitate Screening Authorization Forms sign off and oversee tracking, where applicable
Process documents for signature in DocuSign
Oversight of Clinical Trial Insurance

Clinical Diabetes Specialist

As a Clinical Diabetes Specialist (CDS) you will partner with a Territory Busine...

Location

United States , Orlando

Salary:

Not provided

Sequel Med Tech

Expiration Date

Until further notice

Requirements

Valid professional license in one or more of the following fields: RN, RD, PA, NP, Pharmacist
Certified Diabetes Care and Education Specialist (CDCES) is preferred
2+ years of experience coordinating and conducting diabetes education with strong experience in the technical use of diabetes technology preferred
For Senior role: Certified Diabetes Care and Education (CDCES) certification required
4+ years of clinical diabetes education experience
Experience coordinating and conducting diabetes device education in the medical device industry preferred
Demonstrated history of high performance in previous roles
Excellent presentation skills and ability to respond to questions from patients and healthcare providers in real time
Strong data analysis, evaluation and problem-solving skills
Knowledge of diabetes products and therapies

Job Responsibility

Develop effective territory planning and strategies with TBL to meet/exceed territory goals
Execute clinical selling strategies within assigned accounts
Assess referrals for product use in people with diabetes to confirm criteria are met for product utilization
Facilitate product education and training for users of Sequel products
Drive healthcare provider adoption and confidence in Sequel products by promoting the clinical benefits of automated insulin delivery with Sequel products and conducting impactful product demonstrations
Certify healthcare providers to conduct product training for people with diabetes
Facilitate virtual product training and other educational webinars
Communicate user feedback cross-functionally to solve problems and improve product development
Collaborate with customer care and sales support to optimize the user experience
Consistently exhibit a high level of proficiency and expertise in discussing and demonstrating Sequel products, as well as expertise in diabetes and therapeutic options for diabetes care

What we offer

401k plan with a 6% company match and 100% immediate vesting
Capped out-of-pocket insulin costs and GLP-1 coverage across all plans
Multiple medical plans through Aetna, including a 100% company-paid high deductible plan paired with employer HSA contributions
Vision and dental plans
Employer-paid short-term disability
Voluntary options like accident and pet insurance
Flexible PTO and generous paid holidays

Fulltime

Enterprise Resilience Senior Specialist

As our Enterprise Resilience Senior Analyst, you'll be a seasoned expert leading...

Location

United States , Englewood

Salary:

41.14 - 61.20 USD / Hour

American Nursing Care

Expiration Date

Until further notice

Requirements

Bachelor's Degree, 4 to 6 years of applicable work related experience may be considered
Minimum five (5) years’ experience in Business Continuity, Cyber Resilience, and Disaster Recovery
Minimum three (3-5) years leading large-scale crisis and resilience programs and initiatives

Job Responsibility

Design, manage, and execute a comprehensive training and exercise program (tabletops, drills, functional and full-scale exercises) and lead after-action reviews to validate capabilities, identify gaps, drive remediation, and build system-wide response proficiency
Lead the enterprise business continuity program by planning, developing, and managing global risk, intelligence, and business continuity initiatives to ensure system‑level preparedness, response, and recovery capabilities are designed, implemented, and continuously improved
Serve as the senior subject matter expert and trusted advisor to executive leadership, clinical and operational leaders, cybersecurity, legal, and communications teams
provide guidance before, during, and after incidents and, when needed, act as incident commander, incident manager, or senior advisor to enable timely, coordinated decision-making and recovery
Coordinate cross-functional preparedness and resilience efforts across clinical, IT/cybersecurity, facilities, logistics, communications and other stakeholders, and advise on risk mitigation strategies, policies, processes, and technology improvements to reduce disruption impact
Establish metrics, reporting, and governance for resilience and business continuity planning
prepare briefings for senior leadership and governance committees and track corrective actions to closure to ensure continuous improvement and accountability
Maintain external partnerships and regulatory and industry awareness—public health, emergency management, regional healthcare coalitions, law enforcement, and vendors—and ensure all business continuity activities comply with organizational, legal, privacy, and security requirements

What we offer

medical, prescription drug, dental, vision plans, life insurance, paid time off (full-time benefit eligible team members may receive a minimum of 14 paid time off days, including holidays annually), tuition reimbursement, retirement plan benefit(s) including, but not limited to, 401(k), 403(b), and other defined benefits offerings

Fulltime

Senior Regulatory Specialist

The Senior Regulatory Specialist is responsible for planning, managing, and impl...

Location

United States , Burnsville

Salary:

100000.00 - 130000.00 USD / Year

Imricor Medical Systems

Expiration Date

Until further notice

Requirements

Bachelor of Science in a scientific discipline or equivalent education/ training
5+ years’ Regulatory and/or Compliance-related experience in a regulated industry
Previous experience with US and EU medical device regulatory requirements including Quality Systems and clinical investigations standards
Experience with preparation, submission, and approval for medical devices is required
Strong communication skills, both verbal and written
Strong analytical and problem-solving skills, as well as a good background in the medical device development process
Demonstrated ability to effectively manage multiple projects and priorities
Skills in multiple computer-based tools and software such as Word, PowerPoint, Excel, and Adobe Acrobat

Job Responsibility

Develops domestic and international strategies for regulatory approval of company products
Coordinates, compiles, and submits U.S. and international regulatory filings for new and modified products, including PMAs, 510(k)s, IDEs, CE Marking submissions, and other country-specific product registrations
Develops and maintains positive relationships with regulatory body reviewers through oral and written communications regarding clarification and follow-up of submissions under review
Reviews product and manufacturing changes for compliance with applicable regulations and impact on regulatory filings
Represents RA on cross-functional product development, manufacturing, and clinical support teams and provides regulatory leadership and feedback throughout the product development cycle. Provides recommendations for how to overcome regulatory barriers
Provides technical reviews of supporting documentation for inclusion in regulatory filings
Supports Medical Device Reporting (MDRs) and Medical Device Vigilance Reporting
Represents RA on other cross-functional projects, which may include process changes and continuous improvement efforts
Meets defined goals and objectives through own initiatives, activities, and available resources with minimal supervision
Performs other related duties and responsibilities, as assigned

What we offer

Medical
Dental
Vision
Health Savings Accounts
Health Care & Dependent Care Flexible Spending Accounts
Disability Benefits
Life Insurance
Retirement Benefits

Fulltime

Senior Systems Testing/QA Specialist

Our client is looking for a Senior Systems Testing/QA Specialist for a 3 month c...

Location

Canada , Toronto

Salary:

Not provided

Randstad

Expiration Date

February 10, 2026

Requirements

6+ years experience Hands-on experience with UI and Web Services automation tools such as SOAPUI, Selenium, Selenium WebDriver, JIRA, Dexter, Data Driven automated testing
6+ years experience Knowledge and hands-on experience with FHIR (Fast Healthcare Interoperability Resources) messages and data structures
Minimum 6 to 8 years’ experience testing and automating applications within electronic health-related projects, ideally with experience testing clinical software systems
Knowledge of the Provincial Consent Override Interface (PCOI) application, Consent Management Technology Asset (CMTA) application, Ontario Lab Information System (OLIS), Provincial Client Registry (PCR), SMILE/CMRO system and One Access Gateway (OAG)
Hands-on experience with UI and Web Services automation tools such as SOAPUI, Selenium, Selenium WebDriver, JIRA, Dexter, Data Driven automated testing
Experience working with ORACLE, ETL, SQL databases and queries
Knowledge and hands-on experience with HL7 messages and data structures
Knowledge and hands-on experience with FHIR (Fast Healthcare Interoperability Resources) messages and data structures
Experience with testing RESTful APIs
Experience with testing system accesses based on OAuth authentication/authorization and JWT tokens

Job Responsibility

Contribute towards development of testing strategy, test plans, the selection of testing tools, and the identification of resources required for testing
Provide test estimates to Test lead for assigned testing tasks
Develop and execute manual test cases and test data
Execute functional & system integration testing for UI (User Interface) and backend systems, connectivity/error handling testing, and other test types as defined in the test strategy/plan
Develop and execute robust and dynamic automated test scripts, parameterize test data, and integrate the scripts into an automated test suite
Maintain and update the automated test suite due to changes in functionality
Develop test plans, test scripts and test cases and execute these against the various components
Work with the testing lead and IT lead of each project as well as the project team members in the analysis, design, development, implementation and ongoing support of the required systems

What we offer

Earn a competitive rate within the industry

Senior Clinical Development Specialist

Adtalem Global Education

Location:
United States , Atlanta

Category:
Education

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
January 18, 2026

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Job Description:

Job Responsibility:

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Job Posted:
January 18, 2026