clinical research associate jobs in qatar

Clinical Research jobs in Qatar

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Clinical Nurse - OPC (Genetics)

Sidra Medicine

MAMMOGRAPHER Clinical Imaging Technologist I - Radiographer - Grade 110 - Doha, Qatar

Global Medical Recruiting

• Doha, Qatar

Consultant Clinical Scientist or Physician - Microbiology and Virology

Clinical nurse - picu, mri clinical imaging technologist i - radiographer - grade 110 - doha, qatar, clinical pharmacist specialist (pharmd with expertise: mental health / addiction treatment) - grade 113 - doha, qatar, clinical exercise physiologist.

Power International Holding

Manager - Respiratory Services

Technologist ii - ultrasound (breast ultrasound), respiratory therapy specialist (acute care) - grade 112.

• QAR 19,650 per month

Dietetics Team Leader

Molecular diagnostics technologist, it administrator - hpc, medical surgical nursing manager, technologist i- pathology.

United for Manpower Solutions

Head of Quality Improvement (Healthcare) - Grade 113

Technologist 1 – pulmonary function lab, registered dietitian ii, technologist - eeg, staff scientist - assistant level (bioinformatics), get email alerts for the latest jobs in qatar.

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Clinical Research Jobs in Qatar

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Assistant- Research Laboratory Management

Executive Assistant

Manager - respiratory services.

Clinical Nurse - OPC (Genetics)

Clinical nurse - picu, staff scientist - assistant level (bioinformatics), director - nursing critical care, patient care partner- peds emergency, technologist - eeg, registered dietitian i, consultant clinical scientist or physician - microbiology and virology, social worker ii, senior physiotherapist.

Clinical Nurse Manager - Dialysis / Nephrology / Transplant

Hospitalist - pediatric anesthesiology, patient care partner - fc202170 (unit 7a).

Clinical Research Jobs in Qatar

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Clinical research coordinator.

Day to Day: This opportunity will be part of the clinical trials in a pharmacy. Bringing the trials to the people at their local pharmacy. The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of clinical trials, recruitin More...

Clinical Research Associate

Location: Doha,QADepartment Name: Clinical and Applied Health Research Department QU Health is seeking a full time Research Associate to lead the designated research project in Clinical and Applied Health research field. The individual hired will supervise a small team at the Centre a More...

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Duties & Responsibilities Contribute significantly in designing and implementation of researchmethods and protocols; design safety procedures; adopt new processes,techniques, or instrumentation relative to research procedures. Oversee general laboratory work relevant to assig More...

Clinical Research Nurse

Must Haves: 2+ years of RN experience, preferably in Oncology and/or Clinical Research (clinical preferred over bench, checking in patients, critical thinking, working in ER/ICU, no home health and hospice experience as it doesn't translate well) Graduated from an accredited More...

Clinical Research Associate Cancer Research Uk

What skills will I need? Biological Sciences degree OR equivalent nursing qualification/experience. Working knowledge of ICH/GCP, EU legislation and clinical trial methodology. Proficient in the use of Microsoft Office (TM) - Word, PowerPoint and Excel. Flexible and proactive More...

Research Coordinator

The Research Coordinator provides support to the research Investigator’s projects. (S)he is primarily responsible for the coordination between the various stakeholders of the research projects at Sidra and externally specifically with regard to research subjects recruitment samp More...

Clinical Nurse

Identifies outcomes with regard to patient care delivery and timely care. Assures quality of care by adhering to therapeutic standards, measuring health outcomes against patient care goals and standards; making or recommending necessary adjustments; following hospital and nursing div More...

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Clinical Lead

Mind Institute, an independent, state-of-the-art special needs center in Qatar is dedicated to providing comprehensive care and support to individuals with diverse needs. Our center is committed to enhancing the quality of life for our clients and their families through personalized c More...

Clinical Specialist

KEY DUTIES AND RESPONSIBILITIES: Deliver clinical facilitation to customers at conferences, clinical workshops, training meetings and in-clinic. Work with AMI Lead to determine clinical needs and provide facilitation to customers accordingly. Formulate clinical development plans fo More...

The scope of responsibility, duties and accountability at the facility department and position levels including knowledge and practice of the clinical/technical skills necessary to the position consistent with the Qatar Council for Healthcare Practitioners (QCHP) Nursing/Midwifery Com More...

Clinical Pathologist

Requirements: ▪ Bachelor’s degree in related field ▪ Minimum of 3 years experience. Perform laboratory analyses regarding patient samples to aid in the diagnosis and monitoring of conditions. This includes hematological, biochemical, immunological, microbiological, and molecular More...

Identifies outcomes with regard to patient care delivery and timely care. Assures quality of care by adhering to therapeutic standards, measuring health outcomes against patient care goals and standards; making or recommending necessary adjustments; following hospital and nursing d More...

Specialist - Clinical Risk

Ensure statistical reports and data (from clinical risk key performance indicators, incident reports, sentinel events, claims, and complaints) are generated regularly to monitor compliance with the clinical risk program. Improvement action plans are implemented and monitored. Benchmar More...

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Clinical Nurse - Opc

Provides total individualized patient care and assumes accountability for assessing, planning, implementing and evaluating care, discharge planning for each patient and assessing for current and potential problems. Accurately, concisely and appropriately documents care, interventio More...

US Citizens ONLY! Must be able to get Public Trust Clearance.Government long-term contract! Qualifications: Bachelors Degree in a related field and 8-10 years of experience; Masters Degree and 6-n8 years of experience or high school diploma/equivalent and 12 minimum relevant More...

Clinical Specialist Fellow

Working in a multidisciplinary and unique multicultural environment, the Clinical Specialist Fellowship program includes educational and research opportunities as well as ongoing clinical mentorship to support well-rounded clinicians and future leaders in the field of sports medicine.

The Maintenance Engineer is responsible for proper functioning of Equipment’s in industrial workshops. The Maintenance Engineer leverages deep understanding of maintenance strategies in-order to contribute to day-to-day operational maintenance expertise and leadership and sup More...

Staff Clinical Consultant

Top skills to be successful: You are self-motivated and have an attention for detail You have a passion for healthcare and patient safety You have at least 5 years of pharmacy experience with at least 3 years of experience in a clinical position You can interpret and analyze m More...

Animal Research Technician

Specific Position Duties (responsibilities, Tasks, Essential Functions) . Daily animal care activities to include: feeding, animal observations/identification of clinical concerns, and nail trimming . Husbandry activities to include cage change/cleaning, use of power wash and chemic More...

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Division Chief - Clinical Biochemistry

Reporting to the Chair - Pathology, the Division Chief - Clinical Biochemistry provides clinical, education, research and executive management leadership In Clinical Biochemistry. The Division Chief is a clinical and managerial leader working with the Sidra executive team to develop a More...

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Clinical Research Associate

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Clinical Research Coordinator Associate

🔍 school of medicine, stanford, california, united states.

The Department of Pediatrics, Division of Endocrinology is seeking a Clinical Research Coordinator Associate to perform duties related to the coordination of exercise clinical studies.   Coordinate moderately complex aspects of one or more clinical studies.   Work under close direction of the principal investigator and/or study coordinator/supervisor. Applicants should have working knowledge of IRB application process and experience with common research platforms including, but not limited to: REDCap, Zotero, NVivo, Adobe Sign.

Duties include:

• Serve as primary contact with research participants, sponsors, and regulatory agencies.   Coordinate studies from startup through close-out.
• Determine eligibility of and gather consent from study participants according to protocol.   Assist in developing and implementing a variety of recruitment strategies.
• Coordinate collection of study specimens and processing.
• Collect and manage patient and laboratory data for clinical research projects.   Manage research project databases, develop flow sheets and other study related documents, and complete study documents/case report forms.
• Ensure compliance with research protocols, and review and audit case report forms for completion and accuracy with source documents.  
• Prepare regulatory submissions and ensure Institutional Review Board renewals are completed.
• Conduct study visits and semi-structured interviews, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, acting as primary contact.
• Monitor expenditures and adherence to study budgets and resolve billing issues in collaboration with finance and/or management staff.
• Interact with the principal investigator regularly, ensuring patient safety and adherence to proper study conduct.
• Ensure essential documentation and recording of patient and research data in appropriate files per institutional and regulatory requirements.
• Participate in monitor visits and regulatory audits.
• - Other duties may also be assigned

Stanford University provides pay ranges representing its good faith estimate of what the University reasonably expects to pay for a position. The pay offered to a selected candidate will be determined based on factors such as (but not limited to) the scope and responsibilities of the position, the qualifications of the selected candidate, departmental budget availability, internal equity, geographic location and external market pay for comparable jobs. The hourly pay range for this position working in the California Bay area is between $31.73 to $36.54 based on commensurate experience and background.

DESIRED QUALIFICATIONS:

• Knowledge of Type 1 Diabetes
• Working knowledge of and interest in exercise and physiology
• Experience with common research platforms including, but not limited to: REDCap, Zotero, NVivo, Adobe Sign
• Working knowledge of insulin pumps and continuous glucose monitor (CGM) systems
• Comfort with technology and devices such as fitness trackers; ability to independently troubleshoot challenges with devices and provide guidance to study participants
• Experience and comfort in website development; superior written communication skills to write and develop content for website
• Comfort in conducting literature searches and critically reviewing scholarly literature
• Experience with Zoom; including moderation of Zoom sessions and troubleshooting with study participants

EDUCATION & EXPERIENCE (REQUIRED):

Two-year college degree and two years related work experience or a Bachelor’s degree in a related field or an equivalent combination of related education and relevant experience.

KNOWLEDGE, SKILLS AND ABILITIES (REQUIRED):

·          Strong interpersonal skills.

·          Proficiency with Microsoft Office.

·          Knowledge of medical terminology.

·          Superior attention to detail, time management skills, and ability to manage shifting priorities and deadlines

·          Strong written and verbal communication

CERTIFICATIONS & LICENSES:

Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred.

  PHYSICAL REQUIREMENTS*:

·          Frequently stand, walk, twist, bend, stoop, squat and use fine light/fine grasping.

·          Occasionally sit, reach above shoulders, perform desk-based computer tasks, use a telephone and write by hand, lift, carry, push, and pull objects that weigh up to 40 pounds.

·          Rarely kneel, crawl, climb ladders, grasp forcefully, sort and file paperwork or parts, rarely lift, carry, push, and pull objects that weigh 40 pounds or more.

* - Consistent with its obligations under the law, the University will provide reasonable accommodation to any employee with a disability who requires accommodation to perform the essential functions of his or her job.

WORKING CONDITIONS:

·          Position may at times require the employee to work with or be in areas where hazardous materials and/or exposure to chemicals, blood, body fluid or tissues and risk of exposure to contagious disease and infections.

·          May require extended or unusual work hours based on research requirements and business needs.

~ All members of the Department of Pediatrics are engaged in continuous learning and improvement to foster a culture where diversity, equity, inclusion, and justice are central to all aspects of our work. The Department collectively and publicly commits to continuously promoting anti-racism and equity through its policies, programs, and practices at all levels. ~

• Schedule: Full-time
• Job Code: 1013
• Employee Status: Regular
• Department URL: http://pediatrics.stanford.edu/
• Requisition ID: 104566
• Work Arrangement : Hybrid Eligible

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 School of Medicine, Stanford, California, United States

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Clinical Research Associate - Oncology experience required

• Location: London
• Categories Clinical Monitoring
• __vacancyopjusttionswidget.opt-Business Area__ ICON Strategic Solutions
• __vacancyopjusttionswidget.opt-Remote Working __ Remote

TA Business Partner

• Icon Strategic Solutions

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About the role.

Title: Clinical Research Associate (must have 2 years' experience monitoring Oncology studies within phases 1 and 2 as a minimum) 

Location: United Kingdom, nationwide travel required

Sponsor dedicated 

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

The primary responsibilities of this position include assessing qualifications of potential clinical study sites, implementing clinical studies at participating sites, managing the conduct of clinical studies at sites, ensuring the quality of site performance, and closing clinical studies. This individual will ensure that clinical trials are conducted according to the approved protocol/protocol amendments and complies with Good Clinical Practice (GCP), Company SOPs and all applicable regulatory requirements.

• Responsible for evaluating, initiating, monitoring and closing out clinical study sites.
• Documents all activities in clear, comprehensive and accurate Monitoring Visit Reports, Contact Reports and follow-up letters within required timelines.
• Ensures that the conduct of clinical studies at sites is in accordance with the protocol/protocol amendments, Good Clinical Practice regulations, International Harmonization Guidelines, applicable company Standard Operating Procedures (SOPs), and all applicable regulatory requirements.
• Properly trains/re-trains site personnel on the protocol/protocol amendments, systems utilized in the study, and all operational aspects of the trial.
• Serves as primary contact for site personnel, acting as liaison between site personnel and sponsor study team members.
• Develops patient recruitment strategies in conjunction with the clinical site to meet enrolment timelines.
• Ensures subjects’ rights, safety and well-being are protected.
• Ensures compliance with the procedures to apply in the event of adverse events and serious adverse events.
• Evaluates the quality and integrity of reported data, ensuring that sites enter data into EDC and resolve queries in a timely fashion.
• Assists and supports data validation and data cleaning procedures to ensure timelines are met.
• Identifies, assesses and resolves site performance, quality or compliance problems and develops an appropriate intervention plan for the avoidance of redundant errors and deviations.
• Communicates with Investigators, site staff, Sponsor Study Team Members, and/or QA on issues related to protocol conduct, subject recruitment and retention, protocol deviations, regulatory documentation, site audits/inspections and overall site performance.
• Maintains audit-ready clinical trial documentation. Collects, reviews, monitors, and files required regulatory documentation during study maintenance and at study closeout. Verifies investigator study records are reconciled with the contents of Sponsor files (Trial Master File).
• Verifies the receipt, handling, accounting, storage conditions and availability of study medications under investigation.
• Ensures availability of non-clinical materials for sites.
• Develops strong site relationships and ensures continuity of site relationships through all phases of the trial.
• Gains an in-depth understanding of study protocols and related procedures.

You must have the following to be successful in this role:

• Position requires BA/BS , preferably in the Life Sciences, or RN.
• Minimum of 2+ years of experience in the pharmaceutical / biotechnology industry monitoring as a Clinical Research Associate from study start-up to database lock.
• Strong Oncology monitoring experience in phase 1-3 pharmaceutical/ biotechnology clinical trials.
• Possess good understanding and working knowledge of ICH guidelines, Good Clinical Practices (GCP), PhRMA code, FDA CFR, clinical research ethics, HIPAA and patient privacy laws, and other relevant, local regulatory requirements.
• Good knowledge of concepts of clinical research and drug development.
• Strong working knowledge of EDC, IVRS and CTMS systems.
• Proficiency in the use of the Microsoft Office.
• Ability to handle and prioritize multiple studies and projects.
• Ability to work effectively in a team/matrix environment.
• Ability to understand technical, scientific and medical information.
• Demonstrated strengths in planning, organizational, project management, analytical, oral/written communication, effective time management, conflict management, problem solving, attention to detail, and interpersonal skills.
• Works with high quality and compliance mindset.
• Possess a valid UK driver’s license.
• Must be willing to travel and spend 6-8 days /month on site.
• Ex-US: Proficient in speaking and writing English and the country language when applicable.

What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs
• Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
• Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others

Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below. https://careers.iconplc.com/reasonable-accommodations Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

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To excel as a Clinical Research Associate (CRA) in a Clinical Research Organization (CRO), you need a combination of education, skills, and the right mindset. Brazil-based CRA II Debora shares her

Brazil-based CRA II Debora Oh shares her tips on how to become a great CRA and provides insight into life at ICON.

How to progress as a Clinical Research AssociateTo thrive as a Clinical Research Associate (CRA), it is imperative to cultivate a multifaceted skill set and demonstrate unwavering commitment to exce

 Senior CRA Yemi Moses recounts her development and shares her career ambitions with ICON plc.

Senior Clinical Research Associate Suzaita Hipolito talks about the satisfaction gained from working in Clinical Research. “What would it look like to wake up every day feeling happy and fulfilled?

Senior Clinical Research Associate, Suzaita Hipolito, talks about how working in Clinical Research gives her happiness and fulfilment.

Suzaita Hipolito

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