Jobs updated



Editor – Biomedical Sciences, Physical Sciences & Humanities Dubai

Are you looking for a full time job opportunity that does not require you to travel?

At Cactus Communications, you can join a team of highly skilled editors who are experts in various academic fields. We’re currently hiring Editors on a full time work-from-home basis in the Biomedical Sciences, Physical Sciences and Engineering, and Humanities and Social Sciences.

• Edit manuscripts such that the final text is in standard scientific English and is free of unclear or unidiomatic sentences
• Adhere to job-specific instructions and format manuscripts according to the target journal when required 
• Understand client and industry requirements and adapt working approach accordingly
• Meet deadlines
• Receive training to become adept at the points mentioned above

• Flexibility. You can work from anywhere.
• You will receive training to become adept at editing.
• You will have unlimited access to exclusive interviews with industry experts, articles on the latest industry trends, and publication and writing tips on our learning and discussion platform.
• At CACTUS, you will be exposed to research carried out worldwide and will get an insider’s view of the burgeoning, multi-million-dollar publishing industry.

• A Bachelor’s/Master’s/PhD degree in any sub-specialization of medicine, life sciences, physical sciences, engineering or the humanities/social sciences
• Excellent written English skills and attention to detail
• Familiarity with MS Word, Excel, and PowerPoint


Biomedical Engineer Dubai

Urgently required Biomedical engineer having knowledge of Medical Equipments including (LAB, ENT, OPHTHALMIC, ENDOSCOPY, DENTAl, etc) & software used in healthcare; Minimum 2/4 yrs of experience.Email your CV

Chemist Dubai

Looking for Chemist who is having bachelors or masters in Chemistry,agriculture, candidates who is willing to attend municipality exam for the license. Freshers can also apply. 
preferred Indians. please send cv


Lab Chemist for a Lubricants Company in Ajman

Job Requirements:
- BSc. in Chemistry or Chemical Engineering or equivalent

- Extensive experience in a lubricant and petroleum industry.
- Wide range of knowledge in quality control
- Internationally established standard test methods / testing techniques and instrumental analysis
- Research applicable in particular to testing of crude oil / condensate & petroleum products
- At least should have been in a supervisory position

- Computer literate
- Very Good knowledge of English, both spoken and written
-Should be able to work independently
- High level of technical knowledge and interpersonal skills
- UAE Driving License is an advantage

Medical Technologist Dubai

Medical Laboratory Technologist - DHA licensed required. He/ She should be have excellent work experience in Microbiology , Chemistry and in general routine work

Job responsibilities include:
• Responsible for sample receipt, sample separation and performing a variety of standard sample processing ranging from, hematology, serology, microbiology, endocrinology and chemical laboratory tests when posted in a specific work area.
• Follows established laboratory procedures for specimen handling, processing, test analysis, and reporting. Performs a variety of determinations on different body fluids; confirms and verifies test results and reports findings to Section In-charge.
• Responsible for the accurate performance of assigned duties by supervision received from a higher level Laboratory Technologist or Section In-charge who reviews work for adherence to established policies and procedures.
• Process specimens for laboratory tests and examination in all sections of the laboratory information system; enters and forwards results for verification by the Section In-charge and authentication by Clinical Pathologist & Laboratory Director.
• Performs scheduled maintenance on all instruments; performs and reviews quality controls on testing and notifies Supervisor of any problems and corrective actions taken.
• Operates, calibrates, and conducts performance checks on clinical laboratory equipment.
• Participates in quality management system
Should have 3 to 5 years of work experience in the UAE

DHA License is a MUST.

Britannia Pharmaceuticals Ltd

Pharmaceuticals and Healthcare Analyst Dubai

Reference: JT-896202
Britannia Pharmaceuticals Ltd, the leading provider of global political, economic, industry, financial market and company analysis, requires a commercially astute biological science graduate with the skills and ambition to succeed as a Pharmaceuticals & Healthcare Industry Analyst.

Based in our United Kingdom headquarters, you will be contributing to our Industry service for Pharmaceuticals & Healthcare, providing opinion-driven, analytical research for senior decision-makers in financial institutions, consultancies, government agencies and large multinational corporations.

Britannia Pharmaceuticals Ltd

Clinical Research Associate - CRA Dubai

Reference: JT-896218
Job Summary:
We are urgently in need of a Clinical Research Associate - CRA.

Key Responsibilities

Ensures the integrity of clinical data and adherence to applicable regulatory, protocol and Company guidelines.
Ensures the rights, safety and wellbeing of clinical trial subjects is maintained.
In accordance with COMPANY SOPs, performs site management activities including:
site evaluation visits
site initiation visits
monitoring visits
closeout visits
Collaborates with the Core Project Team to drive subject recruitment
Establishes and maintains regular contact with Investigators, vendors and trial sites to ensure compliance with applicable regulations and the protocol.

Britannia Pharma

Clinical Data Analyst Dubai

Perform CRF/eCRF data validation to ensure data integrity and quality. 
Issuing data queries (DQs) manual or automated and maintenance of CRF according to DQ replies which may involve interpretation and decision making as to appropriate course of action. 
Run, review, action and resolve listings of errors/inconsistencies identified by validation checks. Validate and reconcile vendor data as needed. 
Reconciling the Serious Adverse Events in the CRF/eCRF and Clinical Database with the Central Safety Serious Adverse Events Database. 
Participate in the QC review of study data prior to study release. 
Assist with the review and evaluation of protocol against CRF. 
Report findings to senior staff to assure consistency and accuracy. 
Assist in the development of data validation specifications. 
May serve as initial customer contact by answering basic questions from customers. 
Effectively communicate w/ colleagues and customers to maintain a consistent approach in handling the work. 
EDC (Inform), oncology data management, local and central lab validation experience preferred.