8 Clinical Internship jobs in Egypt

OneHealth is a world-class healthcare provider present in Egypt, Nigeria & expanding in Africa; offering high-quality medical services alongside a unique customer journey. The goal is simple - to revolutionize the healthcare industry through a seamless customer experience, whether it is in physical branches via state of the art medical centers or virtually through 24/7 access to teleconsultation via digital channels.

With a global mindset that aims at elevating the customer healthcare journey, OneHealth medical centers offer one-stop-shop healthcare services by providing access to over 30 medical specialties and sub-specialties, advanced diagnostics, laboratory services, and electronic medical records for all customers, which makes going to the medical center or consulting a doctor virtually, a medical experience like no other!

OneHealth is owned by AXA Group and is on a mission to provide exceptional healthcare solutions in emerging markets serving both insured and non-insured customers; and to make healthcare an affordable, trusted and above all convenient experience that all clients deserve.

**Clinical Psychologist**

**We are hiring for A Medical Center In Saudi Arabia (Riyadh & Dammam) a "Clinical Psychologist"**

**Main Details;**
- **Full Time job - Onsite**
- **Open for Any nationality yet must speak English fluently**
- **Age is not more than 45 Years Old**
- **Package is negotiable**
- **Preferable HAVE EARNED HIS/HER DEGREE / TRAINING ABROAD (BACKGROUND TRAINING ABROAD IN UK, USA OR AUSTRALIA)**

**Role**:

- Clinical Psychologists diagnose, evaluate, and manage various mental health disorders. In a variety of contexts, they deal with individuals, including children, adolescents, and adults, as well as families, couples, and groups.
- They also communicate with other experts, such as psychiatrist to address the challenges of clients.

**Summary**
- Clinical Psychologists assess patients and provide diagnoses of mental, emotional, behavioral, educational, and developmental issues.
- Psychological treatments and procedures are used by clinical psychologists to help patients with a wide variety of mental health issues, such as depression, anxiety, and difficult behavior.
- After conducting an assessment and discussing the client's treatment objectives, clinical psychologists design individualized treatment programs. The treatment can be administered individually or in groups.

**Duties & Responsibilities**

**Diagnosis & Therapy**

1- Identifies and diagnoses psychological, emotional, and behavioral disorders in clients utilizing a variety of assessment approaches such as individual interviews, family interviews, Psycho metrics / assessments, and other appropriate tools. The Medical Director or a recognized international agency must approve all evaluation procedures and tools.

1- Creates and implements treatment plans based on evaluation results to assist the Client in meeting their treatment objectives. To obtain client acceptance on the treatment plan, the treatment plan must be disclosed to the client in the second session but no later than the third session. In the HIMS system, the plan must be clearly recorded.

2- Assessing the effectiveness of programs and making changes as needed.

3- In consultation with the direct Supervisor, provides crisis intervention in cases requiring urgent psychological care.

4- Empathize with a diverse spectrum of people and focus on clients' needs by providing suitable guidance for good behaviors and preventative measures to boost overall mental health.

5- Demonstrate Superior communication abilities to discover complex mental health conditions.

**Administrative & Communication**

1. Manage own schedule, plan appointments for own clients, and maintain a high client retention rate by providing the finest service possible and continually outlining the outcomes obtained so that the client is completely aware of the psychologist's accomplishments.

2. Calls prospective clients to welcome them, answer their inquiries, and persuade them to sign up as RRC clients.

3. Adopts a "Can do" mentality when managing new and evolving jobs to support the efficient running of RRC's many activities, including but not limited to: Administrative tasks, Customer care tasks, and any other task from time to time as per the business needs.

4. Take part in unusual actions as directed or necessary by RRC Management.

**Training & Education**

1. Stay current by continually updating information, performing research, and producing RRC material.

2. Participates in educational programs, in-service meetings, clinician meetings, workshops, research, and report writing to advance professional growth. Provide psychology instruction and training to other team members.

3. Provide clinical supervision to less experienced psychologists and multidisciplinary team members.

4. Create client training programs in partnership with internal teams to improve the attractiveness and delivery of various therapies.

**Documentation & Confidentiality**

1. Ensures that documentation of therapy is completed in compliance with applicable policies and procedures pertaining to medical records; develops, executes, and adheres to policies that ensure the confidentiality of patient information. ensuring that accurate program and client records, in addition to any other papers that may be relevant, are kept and stored in a secure location.

1. Ensure that all services are carried out in accordance with the applicable ethical and professional standards of care.

2. Ensure that all necessary clinical documentation is completed in a timely and correct manner.

**Required Knowledge, Skills, and Abilities**

1. Understanding of the administration, scoring, and interpretation of psychological tests.

2. Understanding of crisis intervention tactics.

3. The ability to monitor, appraise, and record symptoms, emotions, and progress, as well as make individual adjustments.

4. The ability to successfully communicate therapy information, test results, diagnoses, and/or planned treatment to the client in an understa

**Careers that Change Lives**

Medtronic is looking for an Clinical Research Monitor! Be a part of a company that thinks differently to solve problems, make progress, and deliver meaningful innovations.

The Clinical Research Monitor is responsible for the oversight of clinical research conducted at investigational sites to ensure compliance with study protocols, applicable regulatory standards, Ethics Committee/Institutional Review Board (EC/IRB) policies and procedures and business policies. This position works under supervision as needed, working closely with study teams, site personnel, Medtronic field personnel and monitoring supervisor for resolution of site issues.

**A Day in the Life**

We offer you a position where your responsibilities may include the following and other duties may be assigned:

- Perform site monitoring visits in accordance with the study Monitoring plan to ensure compliance with the Investigational Plan, Monitoring Plan, applicable regulatory, IRB/EC, and Medtronic standards, guidelines and policies
- Communicate visit findings with site personnel and complete a written letter for distribution to the principal Investigator and appropriate site personnel for follow-up
- Prepare site visit reports and correspondence for all visits conducted in accordance with the study monitoring Plan
- Identify site needs, provide solutions to facilitate the clinical trial process
- Act as a primary point of contact for study sites as requested
- Assist in initial and ongoing site personnel training as required
- Identification and escalation of protocol deviations, discrepancies in data,and non-compliance to study protocols, applicable regulations, Good Clinical Practices and Standard Operating Procedures
- Collaborates with monitoring management and study team personneltowards securing Investigator compliance
- Understand the study protocol and accompanying backgroundinformation (e.g., Investigator Brochure, Report of Prior Investigations etc.)
- Possess a working knowledge of disease state and investigational product
- Possess understanding of regulatory requirements
- Attend internal department and team meeting as requested
- Adhere to all applicable Medtronic policies and procedures

In addition, the Clinical Research Monitor may:

- Attend Investigator and/or Coordinator meetings
- Provide input into final study site selection
- Be involved in site management activities
- Be assigned lead monitor responsibilities which include but are not limited to:

- Providing input on study protocol, CRFs and other study documents
- Authoring or assisting in the creation of Monitoring Plans, monitoring section of Data Management Plans, and source document worksheets
- Assisting in the creation of corrective and preventive action plans and trending reports
- Managing site assignments in collaboration with manager
- Facilitating communication and information flow between assigned project teams and assigned monitors on project
- Ensuring monitors are trained, current with project requirements and understand study milestones
- Overseeing action item tracking and resolution status
- Performing co-monitoring visits as needed
- Ensuring Monitoring Plan requirements are being met and escalates risks
- Attending Core/Study team meetings

**Must Haves**
- Bachelor or Master degree in life sciences, nursing or other health related disciplines
- Fluent in English and Arabic
- Two (2) years of Clinical Research monitoring experience preferred
- Capable of clearly and effectively communicating verbally and in writing
- Excellent interpersonal skills
- Ability to work in a fast paced environment
- High attention to detail and accuracy
- Excellent problem solving skills
- Competencies and essential skills in the following: cross functional relationships, decision making, execution/results/process improvement, customer satisfaction
- Basic understanding of any applicable regulations (e.g., Good Clinical Practices, ICH guidelines, FDA CFR, ISO, clinical research ethics, HIPAA and patient privacy laws, EU Directive, etc.)
- Regulations/standards training (FDA, ISO, GCP and other country specific training as applicable)
- Ability to handle and prioritize multiple therapeutic areas and projects simultaneously
- Demonstrated ability to maintain composure in difficult circumstances and to identify and adapt to shifting priorities and competing demands
- Experience of conducting clinical research activities in a regulated environment
- Availability for national and international traveling up to 70% of time.

**Nice to Haves**
- Knowledge of any other language
- Proficient knowledge of medical terminology
- Scientific/clinical knowledge needed to adequately monitor the trial (e.g. general therapeutic area education and training)
- Business knowledge or experience with the medical/healthcare industry
- Experience working in a team/matrix environment requiring strong working relationships

**About Medtronic**

Together, we can c

Manage assigned data management project and provide leadership to the data management teams.
- Provide staff training for all projects to which assigned.
- Reviewing data for completeness and consistency
- Ensure adequate QC checks and Database Quality Assessments on the clinical databases
- Ensure timely database locks for all assigned projects.
- Designing CRF as per the sponsor protocol
- Developing Data Validation Plan
- Validation/Discrepancy Management
- CRF annotation
- Coordination of data management and biostatistics activities within a project
- Mentoring and training less experience/Data Administrators
- specific coding tools - MedDRA, WHO drug dictionary and other recognized pharmacopoeia to ensure correctness of coding
- Write clear and concise queries for coding clarification
- Identify the need of study specific coding conventions
- Create and maintain study specific coding conventions when required
- Assist and support clinical data managers in order to identify the specific coded panels and dictionaries / versions to be used
- Coordinate with clinical data managers regarding timing of import / exports of data to the client
- Review coding listings to ensure accuracy and consistency of coded data
- Participate in internal project team meetings and facilitate efficient project communication
- Participate in database lock process and snapshots and ensures that all coding steps prior to locking the database are complete
- Prepare Data Cleaning Specification. Review the Data Validation Specification
- Develop or provide input to project specific guidelines, e.g. SAE handling
- Initiate the running of study specific programs
- Identify and report protocol violations
- Lock site(s) within EDC system - remove user's data modification privileges. Interact with site (via mail) as required
- Perform early and final database QC activities
- Update all relevant tracking system on an ongoing basis
- Keep Manager informed about work progress and any issues to avoid surprises. Requires some interaction / supervision by Manager or assigned mentor.
- Provide consultation, facilitate metrics collection and develop action plans in conjunction with Management to keep project on time and within budget.
- Resolve escalated quality issues.
- Represent Operations Quality Management in audits and inspections as required.
- Perform other duties as assigned.

**Qualifications**:

- Education: Pharmacist / Medicine / Dentist.
- Experience: at least 2 years in Data manager

**Job Overview**
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.

**Essential Functions**:

- Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
- Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
- Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
- Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
- Collaborate and liaise with study team members for project execution support as appropriate.
- If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.

**Qualifications**:

- Bachelor's Degree Degree in scientific discipline or health care preferred. Req
- Requires at least 2 years of year of on-site monitoring experience.
- Equivalent combination of education, training and experience may be accepted in lieu of degree.
- Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.
- i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Good therapeutic and protocol knowledge as provided in company training.
- Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
- Written and verbal communication skills including good command of English language.
- Organizational and problem-solving skills.
- Effective time and financial management skills.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world. Learn more at

**Aortic stenosis impacts millions of people globally, yet it often remains under-diagnosed and under-treated. Edwards' groundbreaking work in transcatheter aortic heart valve replacement (TAVR) pioneered an innovative, life-changing solution for patients by offering heart valve replacement without the need for open heart surgery. Our Transcatheter Heart Valve (THV) business unit continues to partner with cardiologists and clinical teams to transform patient care with devices supported by clinical evidence. It's our driving force to help patients live longer and healthier lives. Join us and be part of our inspiring journey.**
**How you will make an impact:**
+ Develops clinical education materials in connection with clinical investigations. Provides expertise and clinical insights on the device, procedure and protocol throughout the life cycle of the clinical investigation.
+ Responsible for certification of the centers, physicians and other related staff, as well as EW personnel and as outlined within EW SOPs
+ Interact with KOL and proctors
+ Provide education on all aspects of the device, device handling, implantation and troubleshooting techniques related to equipment, tools and products required for device implants.
+ Develop and continuously improve training curriculum, training materials and training tools, based on clinical trial experience, EW guidelines and SOP.
+ Business Intelligence
+ Educate and train physicians, hospital personnel and hospital staff on technical matters related to products and procedures through conducting and/or coordinating one-on-one ad hoc training sessions and in-service structured education programs.
+ Throughout commercial procedures, provide physicians and medical staff with required follow-up support to ensure continuity of education and technical support related to all aspects of patient outcome.
+ Plan and implement growth strategies within focused accounts in partnership with the Sales and Sales Management
+ Responsible for upselling in key strategic accounts working in conjunction with Business Managers
+ Learns the product(s), physiology, anatomy, applications of the market and Edwards Lifesciences
+ Reviews clinical support activities, changes in the market and assigned accounts, as well as, competitive activity with the NSM and the appropriate Sales Specialist.
+ Understand key market in structural heart business in Egypt
**What you'll need (Required):**
+ 2-3 years of previous related experience in medical device and/or clinical experience
+ Bachelor's Degree in related field
+ Willingness to travel
+ Good knowledge and understanding of cardiovascular science
+ Good understanding of cardiovascular anatomy, pathology and physiology
+ Good understanding of medical device regulatory requirements and documents, device accountability and adverse events reporting
+ Training experience in clinical / technical environment
**What else we look for (Preferred):**
+ Familiar with Cath lab environment
+ Transcatheter Structural heart therapies experience
+ Preferred Location: Cairo, Egypt
+ Proven expertise in MS Office Suite and ability to operate general office machinery
+ Good written and verbal communication skills, presentation, and interpersonal relationship skills including negotiating and relationship management skills
+ Good problem-solving and critical thinking skills
+ Ability to manage confidential information with discretion
+ Strict attention to detail
+ Ability to interact professionally with all organizational levels
+ Ability to manage competing priorities in a fast paced environment
+ Must be able to work in a team environment, including inter-departmental teams and representing the organization on specific projects
+ Ability to build productive internal/external working relationships
+ Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control

**Job Overview:**
Local Clinical Project Management services provides local management of a clinical trial (or Medical Affairs data generation activity) in a country or countries. Services/deliverables include operational oversight of assigned protocol(s) at the country level from start-up through to database lock and closeout activities. Further, services will ensure the local trial team is delivering quality data and trial documents/records that are compliant with the assigned clinical trial protocol, company Standard Operating Procedures (SOPs), International Conference on Harmonization for Good Clinical Practice (ICH-GCP), and regulatory requirements. Partners with the Clinical Trial Assistant (CTA)/Investigator Document Assistant (IDA), Site Manager (SM) and Central Trial Manager (CTM)/Global Trial Manager to ensure overall study delivery at the country level.
**Deliverables:**
+ Services rendered will adhere to applicable sponsor's SOPs, WIs, policies, codes of Good Clinical Practice (GCP), local regulatory requirements, etc.
+ Complies with relevant training requirements.
+ Contribute to quality Site Selection
+ Ensures local/country team is meeting recruitment targets with high quality data on time and within study budget
+ Act as primary contact for assigned trial at the country level, may attend/participate in Investigator Meetings as needed. May schedule and conduct a local/country investigator meeting.
+ Drive study compliance
+ Contribute to site level recruitment strategy and contingency
+ Delivers competent vendor management at the country level
+ Ensures high standards for study monitoring
+ Contributes to patient understanding of protocol and patient safety
+ Ensures trial subject safety
+ Ensures Inspection readiness
+ Keeps oneself inspection ready and knowledgeable for current work by complying with relevant training requirements and developing therapeutic knowledge enough for role and responsibilities.
+ With focus on quality and compliance, will work closely with CRAs to ensure CAPA is implemented for audits/inspections or any quality related visits. May conduct accompanied site visits with CRAs, if delegated by FM.
+ Ensure accurate finance reporting and trial delivered within budget
+ Keeps the trial in compliance with local regulatory requirements by organizing and ensuring IEC/HA approvals in cooperation with the local Start Up team, if as applicable.
+ May contribute as a trainer of systems/processes or provide input to functional area in process initiatives, if applicable.
+ Full utilization by timely and accurate time reporting.
+ Experience in management and startup of complex Early Phase trials projection with internal matrix clinical teams and sites, as applicable.
**Education and Experience Requirements:**
+ BA/BS degree.
+ Degree in a health or science related field.
+ 2 years of local trial management or mutually agreed clinical trial experience.
+ Fluency in Arabic and English
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
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