28 Clinical Staff jobs in Egypt

Company Description

COB Solution empowers medical providers with efficient operations, optimized workflows, and innovative solutions to enhance patient care and accelerate growth. Our mission is to provide the tools and support necessary for healthcare professionals to thrive in today's dynamic medical environment. We focus on creating seamless experiences for both providers and patients, ensuring that the primary goal of exceptional patient care is always met.

Role Description

This is a full-time on-site role for a Clinical Assistant, located in Qesm El Maadi. The Clinical Assistant will be instrumental in providing the necessary on-the-ground leadership and operational support to drive our clinics' success. We believe this position will significantly improve our efficiency, accountability, and ultimately, our patient care.

Key Responsibilities:

Daily Operational Oversight:

Oversee the daily operations of up to six assigned clinics.

Ensure all physical therapists (PTs) and patient care coordinators (PCCs) are clocked in at the start of each day.

Proactively follow up on any staff absences or tardiness and implement immediate coverage.

Staff Coordination & Coverage:

Coordinate coverage for any staff members who call out or submit a request , working closely and efficiently with the central operations unit.

Act as the primary point of contact for staffing adjustments and emergency coverage needs within their assigned clinics.

Administrative & Scheduling Management:

Audit the PCC's daily tracker hourly, ensuring all appointments are accurately scheduled, correctly updated, and co-payments are collected in real-time.

Maintain frequent and proactive communication with assigned clinics to anticipate and resolve operational issues.

Ensure smooth patient flow and optimal scheduling practices.

Documentation & Compliance Support:

Provide timely reminders to PTs regarding the completion of documentation throughout the day, ensuring adherence to same-day completion policies.

At day's end, ensure all documentation is complete, the daily tracker is accurately filled out, upcoming appointments are scheduled for all patients.

Patient Retention & Experience:

Complete and maintain the retention sheet for PTs, meticulously noting reasons for patient non-return and identifying trends.

Actively track and work toward specific targets, including visit numbers, patient retention rates, Google reviews, and patient survey completion.

Perform quality assurance tasks, such as randomly calling patients for feedback, addressing any complaints promptly, and ensuring a positive patient experience.

New Staff Onboarding & Support:

Support new PTs and PT Assistants during their initial days in the assigned clinics, ensuring proper account and credential setups (e.g., WebPT access, email setup).

Familiarize new staff with clinic-specific operational procedures and protocols.

To answer all questions related to the operation and departments and help them submitting requests.

Performance Monitoring & Reporting:

Monitor and report on key operational KPIs for their assigned clinics, including visit numbers, retention rates, Google review accumulation, and patient survey scores.

Identify areas for improvement and propose solutions to optimize clinic performance.

Requirements:

Educational Background: Bachelor's degree required. A background in Physical Therapy (e.g., PT, PTA, or extensive experience in a PT clinic setting) is strongly preferred.

Experience: Preferred of 3-5 years of experience in an office management, operations, or supervisory role, preferably within a healthcare or physical therapy environment.

Language Proficiency: Excellent command of the English language, both written and verbal, is essential for clear communication with staff, patients, and management.

Communication Skills: Exceptional interpersonal and communication skills, with the ability to manage diverse personalities and situations professionally and effectively.

Organizational Skills: Superior organizational abilities, attention to detail, and capacity to manage multiple priorities simultaneously.

Technical Proficiency: Proficient in office software (e.g., Microsoft Office Suite) and experience with EMR/scheduling systems (e.g., WebPT) is highly desirable.

Leadership & Problem-Solving: Proven ability to lead, motivate, and problem-solve effectively in a fast-paced environment.

Accountability: Strong sense of ownership and accountability for clinic performance and staff adherence to policies.

Company Description

Talent Solutions plays a crucial role in supporting companies in optimizing their workforce and achieving business objectives through customized solutions. Our mission is to provide businesses with top-notch HR consultation services to help them optimize their workforce and create a positive and productive work environment. We offer a range of services including business consultation, workforce management solutions, hiring services, payroll services, performance management, training, and medical insurance. Our vision is to ensure that an organization's workforce is equipped to drive success and growth.

Role Description

This is a full-time on-site role for a Clinical Supervisor based in Cairo. The Clinical Supervisor will be responsible for overseeing clinical staff, providing clinical supervision, conducting case management, and applying behavior analysis. Daily tasks include supervising client assessments, developing and monitoring treatment plans, offering support and training to clinical staff, and ensuring all clinical practices comply with organizational policies and regulatory guidelines.

Qualifications

• experience in clinics management from 3 to 6 years
• Skills in Applied Behavior Analysis and Psychology
• Strong Supervisory Skills and experience in Clinical Supervision
• Proficiency in Case Management
• dentist doctor are preferred
• Excellent organizational and leadership abilities
• Master's degree in a related field such as Clinical Psychology, Social Work, or equivalent is a plus
• Relevant certifications are a plus
• Strong communication and interpersonal skills
• Ability to work effectively in a team environment

You will be a practitioner on our telehealth platform 'Intellect', where your role is to support our clients' mental health and personal growth based on the individual needs and goals. This is delivered primarily through scheduled 60-minute video sessions on our platform.

This is a freelance remote role with the flexibility to decide your business hours. Local candidates are preferred but others can still be considered. This role is a great opportunity to supplement your current job or private practice.

We're seeking to partner with Clinical Psychologists and Counsellors to be part of a community working collaboratively to bring greater mental health access to the public to provide mental health coaching

What You'll Do

• Provide 1-on-1 telehealth/or onsite mental health support for Intellect's clients
• Focus on clinical cases such as depression, anxiety, trauma, schizophrenia, eating disorders, addiction etc.
• Collaboratively work with the internal clinical team by suggesting improvements to the program and the platform

Requirements

Requirements

• Has a Masters in Counselling or Clinical Psychology
• Candidates must be skilled in Cognitive Behavioural Therapy or other evidence-based approaches (e.g. Motivational Interviewing, DBT, SFBT, etc.)
• Candidate must have at least 300 clinical hours post masters degree
• Candidate can communicate in English and their local language
• Candidates with prior experience in EAP, counselling working adults or coaching managerial roles is a plus
• Candidates who are open to working onsite if necessary is a plus

Our leading EMS organization is searching for an experienced and energetic nutritionist to join our dynamic team.

In this position, you will coach our precious clients with professional health and nutritional advice on how to implement and maintain a healthy lifestyle concurrently with the provided EMS sessions. As a specialist in food science and good nutrition, our clients will seek your guidance towards better eating and exercise habits to reach their ultimate goal of a better healthy life.

Nutritionist Responsibilities:

Evaluate the dietary needs of a client by assessing their health and exercise levels, sleep, and food habits etc.

Clarify information to clients and explain the effects of nutrients on their overall health conditions.

Keep knowledge of EMS features, techniques, and benefits of EMS training.

Demonstrate our EMS service features and benefits to clients and explain how it can serve their goals.

Provide comprehensive evaluation of clients past & present medical conditions to ensure their safety.

Coach clients and suggest positive alterations in nutrition to address clients ' dietary restrictions.

Create full and personalized nutrition plans that promote healthy lifestyles according to individual client's goal.

Set clear objectives, short and long-term goals. Maintain ongoing coaching follow ups with clients to ensure their progress is

on track.

Ensure being updated on the latest nutritional diets and trends

Nutritionist Requirements:

Bachelor's degree in nutritional science, dietetics, or relevant field.

A minimum of 2 years' experience as a professional nutritionist

In-depth knowledge of biochemistry, research methods, and human physiology.

Excellent communication and presentation skills.

A critical thinker with outstanding interpersonal skills.

The Clinical Project Lead (CPL) will work in the Clinical Operations with an emphasis placed on ensuring the highest ethical and clinical standards.

• The CPL assumes responsibility for an individual project or many projects, for one or more Sponsors and reports on the project level to the Account Operations Manager (AOM) responsible for that Sponsor's account.
• The CPL is the liaison with the Sponsor and communicates in an optimal way, making sure that the specific Sponsor's objectives are met.
• The CPL is the leader and the responsible for the project team. The CPL plays an active role in the planning and monitoring of the study.
• The CPL might be required to act as CRA III and act as back-up CRA where needed.

The Position is for MENA Region

Applicant should have as a minimum:

• 6 years of experience as a Clinical Project Lead
• Bachelor's degree in a health-related field
• Working knowledge of relevant regulations related to clinical research studies, ICH Guidelines and GCP
• Business proficiency in English & use of Office Suite
• Excellent organizational and communication skills
• Detail oriented

1. Provide technical and clinical expertise during the sales process by demonstrating the full range of ultrasound products including potential uses, product capabilities, and benefits to customers.

2. Develop and deliver product training to customers on equipment use.

3. Monitor customer installations of ultrasound products to improve customer satisfaction and maintain customer relationships.

4. Support trade shows and professional conferences by performing product demonstrations and customer training.

5. Support the development and execution of marketing strategy and plans. Coordination of internal supporting functions in order to ensure smooth implementation of marketing initiatives and key performance indicators. Work closely with sales manager for marketing planning and execution.

6. Key Opinion Leader (KOL) development and management.

7. Responsible for supporting content marketing. Organization of webinars, seminars, and other online and offline marketing activities.

8. Cooperate closely with global marketing and sales teams to develop new business opportunities and channel development initiatives.

Pharmaceutical Development Company is a leading clinical research organization, providing a Full-Service End-to-End Solution for Phase I to IV clinical trials and NIS /RWE studies in the Middle East and Africa region. Our clients include pharmaceutical, biotechnology, medical device industries, other CROs, and academic organizations. Our team is experienced in managing clinical projects from beginning to completion, PDC has been recognized among the leaders as Clinical Research Organization in the region.

Due to our successful development, we are looking for highly motivated and responsible candidates for the position of:

Name of position: Clinical Project Manager- Location: Egypt

Essential Functions and Other Job Information

1. Being and serve as the first point of contact to client.
2. Coordination and control over the feasibility, start-up, clinical and site-management activities related to a specific clinical trial within the Division.
3. Strict control over the compliance of study milestones: start, patients' enrolment (overall study) and timelines as per the contract obligations.
4. Control over budget, issue, task, and time management of the project/s under their supervision.
5. Oversights of submission/ approval process to EC/ RA.
6. Communication with sponsors, partner CROs, physicians, third parties and regulatory authorities.
7. Manages the process of creation, approval of all essential documents developed or tailored in-house as ICF, patient material and translated documents.
8. Responsible for distribution within the team of final approved version of all essential documents (Protocol, IB, CRF, ICF, etc.).
9. Initiate qualification and approval, ongoing management, oversight and dealing with all third parties involved in the study; complete re-assessment activities.
10. Develops and communicates all study specific plans as PMP, monitoring plan, TMF maintenance plan, communication plan, quality plan, project risk matrix (if applicable) as well as any other study-specific instructions and guidelines.
11. Ensures on time study team trainings, meetings, and customization of study-specific forms and plans.
12. Control over all logistic procedures related to the study.
13. Identify changes, work with team members to quantify financial/ time impact and communicate those changes to appropriate personnel.
14. Ensures the contracting process, when required.
15. Timely coverage of all assigned trainings.
16. Adheres to the rules and regulations of ICH-GCP and other regulatory and ethical guidelines and data protection regulations.
17. Coordinates activities between different stakeholders and determine interim study time points.
18. Providing any requested internal progress reports and completion of the relevant files.
19. Preparation and conducting of Investigator Meetings in close collaboration with the client.
20. Collaboration with internal/ external auditors, co-monitors, or regulatory inspectors in review of files and patient data.
21. Executes any activities in compliance with applicable SOPs, instructions, and principles.
22. Development and update of company SOPs and policies in close collaboration with Management.
23. Support Business Development activities in terms of meetings and budget development as applicable.
24. Supervises and assesses the performance of team members and provides feedback to respective line manager/ HR for appraisal.
25. Perform CPL activities as per assigned clinical trials in all cases as deemed necessary by superior management levels, while avoiding risk of conflict of interest.

Education and Experience

• University degree with life science background or equivalent and relevant formal academic/ vocational

qualification.

• At least 6 years of experience in the field of clinical research; Managing at least 5 Interventional CT.

Knowledge, Skills, and Abilities

• Advanced knowledge of GCP guideline and all applicable clinical research requirements

• Proficiency in English language

• Leadership and good sense of teamwork

• Excellent analytical, organizational, negotiation and decision-making skills

• Ability to communicate information and ideas so others will understand; with the ability to listen to

and understand information and ideas presented through spoken words and sentences.

• Good time management and multitasking skills to coordinate several issues simultaneously.

• Solid interpersonal skills

• Ability to access and use a variety of computer software developed both in-house and off-the-shelf.

• Appropriate MS Office Skills

• May interact with others, relating and gathering sensitive information. Interaction includes diverse

groups.

• Performs a wide range of variable tasks as dictated by variable demands and changing conditions based on task prioritization.

• Ability to perform under stress.

• Regular and consistent attendance

Working Conditions and Environment

• Work is performed in an office or clinical environment with exposure to electrical office equipment.

• Often travels/ drives to site locations. Frequent travel both domestic and international.

The Company Offer:

• Job-specific training

• Work for successful international company, excellent career development opportunity in a perspective professional field

• Very competitive remuneration package

• Additional benefits related to work performance.

Website

The Assigned Country: Egypt

Only short-listed candidates will be contacted for interviews.

Note: By submitting your application, you agree that your personal data will be processed by PDC in accordance with the applicable Data Protection Law and in strictly keeping your confidentiality.

Job Overview

Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.

Essential Functions

• Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.
• Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
• Assist with periodic review of study files for completeness.
• Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
• Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
• Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
• May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.

Qualifications

• High School Diploma or equivalent Req
• 3 years administrative support experience.
• r.
• Equivalent combination of education, training and experience.
• Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.
• Written and verbal communication skills including good command of English language.
• Effective time management and organizational skills.
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
• Awareness of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training.
• Knowledge of applicable protocol requirements as provided in company training.

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

We're Hiring Join Our Team at GMC

Exciting opportunity GMC is looking for Senior Clinical Pharmacist

Responsibilities & Duties:

• Performing daily rounds on hospitalized patients and review patient profile, analyze all laboratory data and record all required patient information to identify, prevent, or mitigate drug-related problems, improper drug or dose selection, sub therapeutic dosage, over dosage, adverse drug reactions, drug interactions, failure to receive drugs, untreated indications, medication use without an indication, and treatment failures.

• Designs and implements stewardship activities and restriction/surveillance programs & ensures the appropriate compliance of healthcare staff to them.

• Develops staff training & orientation programs related to appropriate medication use to facilitate experiential education & practice advancement of healthcare staff.

• Attending the Daily Medical Meeting with physicians to review all clinical pharmacy daily activities & negotiate about any pending issues related to the patients' treatment plan.

• Planning for the clinical pharmacy schedule according to workload and expected flow of shifts to maintain all provided services with the same level of patient care.

• sharing and implementing GMC policies & procedures of medication monitoring and control and ensuring compliance to policies

Requirements:

• Bachelor's Degree in Pharmaceutical Sciences.

• Experience 1-2 years in hospital field in the same title.

• Pharm-D or Board of pharmcy specialties (BPS) is a Must.

• Very Good Excel.

• Interested candidates kindly send your updated CV at

• mentioning (Senior Clinical Pharmacist) in the subject.