Senior Clinical Application Specialist Job at PaxeraHealth (Cairo)

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

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 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 Physician, Patient Safety

Join our dynamic Patient Safety team as a Senior Physician where you'll leverage...

Location

United States; Canada , Remote; Alberta

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Experience in clinical medicine (general or specialist qualifications) which is expected to be kept up to date
Good knowledge of drug safety and the drug development process
Good knowledge/understanding of medical terminology
Relevant experience in pharmacovigilance/ Drug Safety/ Clinical Practice
3 - 5 years previous experience in pharmacovigilance and/or medical monitoring is required
US Board Certification/board eligibility or regional equivalent for Canada
Bachelor of Medicine, Bachelor of Surgery (MBBS) / Doctor of Medicine (MD)/ Medically qualified from an acknowledged Medical School
Completion of at least basic training in clinical medicine (residency, internship etc.)
Demonstrated success in technical proficiency and scientific creativity
Good presentation and verbal/written communication skills

Job Responsibility

Maintaining a good working knowledge of the Adverse event/Safety profile of assigned products, labeling documents, data handling conventions, client’s guidelines and procedures, and global drug safety regulations and guidelines
Maintaining an awareness of global regulatory requirements, reporting obligations and organizing workload to ensure compliance with internal and regulatory timelines for adverse event reporting
Performing medical review of cases not limited to (including complex and challenging cases requiring expert judgement)), clinical trial, and literature cases including combination products {drug-device}) according to client/Parexel Standard Operating Procedures (SOPs
as applicable) and liaising with the client, as require
Writing Pharmacovigilance/Marketing Authorization Holder (MAH) comment and assessing company causality
Review appropriateness of medical content in narrative for medical coherence
Assessing seriousness, listedness / expectedness of reported events
Providing medical inputs to case processing team
Raising appropriate follow-up queries for relevant information from the reporter/HCP (Health Care Professional)
Review and verify appropriate selection of adverse events from source documents, assign appropriate Medical Dictionary for Regulatory Activities (MedDRA) code, review narrative

What we offer

Flexible approach to work that meets your personal needs
Work from home
Benefits vary by country
Investment in your professional and personal development

Senior Clinical Research Associate II - FSP

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...

Location

Turkey

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Extensive knowledge of clinical trial methodologies, ICH/GCP, Food and Drug Administration (FDA) and local country regulations
Monitoring Experience: Minimum 5 years relevant experience in clinical research site monitoring (preferably 3 years in Oncology)
Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
Global clinical trial experience
Must be fluent in English and in the native language(s) of the country they will work in
Significant travel (60-80%) within area is required. May require some international travel and some weekend travel
Valid driver’s license and passport required
Demonstrated knowledge of clinical research and development processes and ability to gain command of process details
Demonstrated knowledge of global and local regulatory requirements
Demonstrated understanding of key operational elements of clinical research (e.g., monitoring, data acquisition and cleaning, reporting, etc.)

Job Responsibility

Oversight of Monitoring Responsibilities and Study Conduct
Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and client standards to achieve project goals, timelines and quality
Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to database lock, ensuring relevant timelines and quality deliverables are met
During study conduct, serve as the primary point of contact for assigned investigator sites. Work in partnership with and/or escalate to the SCP to ensure quality of site delivery
Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites
Partner with SCP to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients
provide protocol training to, and address protocol related questions from the investigator site staff when required, including discussions on known/anticipated operational and clinical trial risks
Attend investigator meeting when required (virtual or F2F). Provide enrollment support and ensure progress by responding to site activation and recruitment issues from investigators. Partner with SCP and the study team to define and support recruitment initiatives at site level
Conduct onsite, remote/electronic monitoring as needed for study site initiation, routine monitoring and study site closure activities and ensure these are conducted accordance to the SMP, Standard Operating Procedures (SOPs) and commensurate with emerging issues and technologies
Monitor site level adverse events (AEs) and serious adverse events (SAEs) and collaborate with the Drug Safety Unit and follow-up with investigators sites, as needed, to bring SAE reports required information to resolution

What we offer

Flexible work arrangements
Career growth and development
Supportive and inclusive environment
Diverse therapeutic areas and project exposure
Advanced Technology

Life Science Administrator

Temporary Life Science Administrator role for a pharmaceutical organization work...

Location

United Kingdom , London

Salary:

14.20 GBP / Hour

Office Angels

Expiration Date

Until further notice

Requirements

Life Science background
Relevant Life Science degree
Strong knowledge of Microsoft Excel

Job Responsibility

Manage the agency database(s) and check consistency between public registers
Inputting applications on the Agency databases and supporting the application specialists with allocation of both clinical trials applications and monitoring of timelines
Assists with generating performance measures for UK trial, and trial registration and summary results posting
Work with the application specialists in data analysis, presentation of Unit metrics for reports and enquiries as required
Assist the Business Support Manager and Operations Lead in implementing Internal Quality Measures and Scientific Advice Meetings
Assist the Senior Safety Manager with finance aspects of new fees from clinical trial annual safety reports

What we offer

Weekly pay every Friday
Easy timesheet accessibility with mobile support
Up to 29 days annual leave
Perks at work and discount schemes for all major retailers and over 150 high street stores
Access to free eye-care vouchers and discounts towards glasses for VDU purposes
Access to well-being platforms
FREE access to online LinkedIn Learning courses
Temp of the Month awards
Dedicated consultant to support your job search and offer expert interview tips

Fulltime

Senior Specialized IT Consultant

Our client is looking for a Senior Specialized IT Consultant for a 12 month cont...

Location

Canada , Toronto

Salary:

Not provided

Randstad

Expiration Date

February 24, 2026

Requirements

5+ years experience Comprehensive understanding of health care sector workflows and source system technologies (such as HIS, EMR, LIS), along with hands-on experience working with Integration Engines
7+ years hands-on experience in delivering electronic health data integration projects or operations, including expertise in the acquisition, integration, and utilization of health data employing healthcare interoperability standards such as HL7 V2.x (mandatory) and V3
5+ years experience Applied knowledge of HL7 Health Standard message conformance tooling (e.g., Caristix, XMLSpy, 7Edit, Postman, etc.) for HL7 v2.x, v3, and FHIR
In-depth knowledge clinical workflow and technical processes within hospitals or other healthcare sector locations
with knowledge on the flow of information using HL7 standard-based messages
Minimum of 7 years of applied experience delivering electronic integration of health data related projects, including integration and adoption initiatives using applied knowledge of healthcare systems, healthcare integration standards such as HL7 V2, V3 and FHIR, XML messaging principles, techniques and technologies is mandatory
In-depth working and applied knowledge of healthcare systems, healthcare integration standards such as HL7 v2 & FHIR, XML messaging principles, techniques and technologies is mandatory (for example Meditech, Cerner, and Epic)
Applied use and knowledge of HL7 health standards, and the application of HL7 messaging standards (HL7 versions 2, version 3 and FHIR), HL7 v3 products including CDA, and related implementation guides from multiple standards development organizations
Applied knowledge of health standards validation & conformance tooling (e.g., Postman, Caristix, XML Spy, 7Edit, etc.)
Excellent verbal and written communication skills for effectively conveying Ontario Health's conformance testing and validation activities in data acquisition and integration projects to technical staff, project managers, and clinical SMEs

Job Responsibility

Performs as a Clinical Data Conformance & Integration Specialist supporting data adoption (contribution) and integration projects, working directly with Senior Project Managers and Product Teams
Provides oversight and HL7 v2 & HL7 FHIR subject matter expertise on Ontario Health data adoption and integration projects, focused on the expert guidance for the review, conformance testing, validation, and implementation of healthcare organizational patient data to Ontario Health clinical data repositories (e.g., ADT data, lab data, clinical data, etc.)
Leverages HL7 v2 & FHIR data standards expertise, clinical expertise and HL7 health information exchange standards experience to successfully evaluate and advise external clients and stakeholders’ technical development of their local interfaces, in readiness for contributing to, or consuming data from Ontario Health clinical data repositories or assets
Manages simultaneous work packages for data contribution projects, ensuring contributed data from external stakeholders adheres to HL7 v2 and FHIR standards, in alignment with the Ontario Health EHR input specifications and FHIR IG’s
Determines readiness of data submission to the EHR product repositories and assets, by conducting expert HL7 v2 & FHIR messaging standards review, evaluation and validation of data compliance, conformance, and readiness for data contribution
Acts as a senior specialist with external clients, stakeholders, partners, and data sources through a defined data integration methodology designed to measure data conformance and validation of contributed data to the EHR
Works with a medium-high level of autonomy based on direction from Leads and/or Management
as well as delivery against set objectives and support scenarios but proactively actioning and resolving issues with minimal supervision

What we offer

Earn a competitive rate within the industry

Fulltime

Senior Speech & Language Therapist

At Orchard Community Care (Disability Services) we are pleased to add to our Mul...

Location

Ireland , Sligo, Galway

Salary:

Not provided

Orchard Care Group

Expiration Date

Until further notice

Requirements

A recognised third level qualification in Speech and Language Therapy
A minimum of 3 years full time post-qualification experience, preferably working with children and young adults with disabilities
FEDS (Feeding, Eating, Drinking, and Swallowing), certification or significant experience with FEDS -related cases
Be registered, or be eligible for registration, as a Speech & Language Therapist by the Speech & Language Therapists Registration Board at CORU
Previous clinical experience in leading specialist referrals in FEDS and other medical conditions affecting swallowing
Strong clinical, communication and leadership abilities, with an Orchard Care Values approach
Must have valid Garda Clearance and valid Overseas Clearance (if applicant lived abroad for more than 6 months)
Full Drivers licence with eligibility to drive in Ireland & access to a vehicle
Be eligible to work in the state without restriction

Job Responsibility

Provide comprehensive speech and language therapy assessments and interventions to children and young people with complex disabilities focusing on enhancing their communication and functional abilities and participation in daily activities
Working with Person In Charge and frontline staff to develop accessible materials for information and social stories purposes
Demonstrates exemplary clinical skills in SLT assessment intervention and diagnostics to meet the specific needs of children and young people with a range of disabilities including physical, sensory, autism, etc
Provide a speech and language therapy service to include communication assessment, diagnostics and intervention, and ongoing service delivery to children and adults with a range of disabilities
Develop individualised treatment support plans based on evidence-based practices
For referred individuals evaluate swallowing function, provide strategies for safe and effective eating and drinking, lead onward specialist referrals in FEDS area and other medical conditions affecting swallowing
Collaborate with the multidisciplinary team other MDT members in an interdisciplinary model and support the Regional Directors to provide holistic care
Engage with families and care giving staff to provide education and support regarding their child’s supported individual communication needs
Participate in service development initiatives and quality improvement projects
Provide education, training, and support to team members providing care to empower them to facilitate the development of the people we support

What we offer

Comprehensive induction process
Extensive training programme
On-going mentoring and support
Continuous Professional Development support
Career progression opportunities
Orchard Values Champion Award
Refer a friend initiative
Working in a well-resourced environment with access to the multidisciplinary team
Employee Assistance Programme for staff and their families

Senior Clinical Application Specialist

PaxeraHealth

Location:
Egypt , Cairo

Category:
IT - Software Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
December 11, 2025

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