شركة ايكون لتصنيع المستحضرات الصيدلانية تعلن عن شواغر وظيفية لديها في الكويت للتخصصات ( الادارية

 

Kuwait Jobs Today: ICON Strategic Solutions Company announces new job opportunities. Are you looking for job opportunities in Kuwait? ICON Strategic Solutions Company announces the opening of recruitment for many jobs in various specializations in Kuwaiton today’s date. These opportunities are available to all nationalities. Learn about the available jobs and how to apply through the following advertisement. ↔️

≥3 years’ experience as medical writer or equivalent

Experience from the pharmaceutical industry or equivalent

Regulatory documents writing experience, submission documents writing experience is a must

Experience with a broad range of different medical writing tasks 

What You Will Be Doing

Support Study Clinical Scientist in medical surveillance and medical monitoring activities under the guidance of the Medical Monitor; conduct daily medical surveillance of laboratory & ECG alerts including review of eligibility criteria as appropriate.

Provides analytical support of clinical trial data, including assessment and follow-up of issues relating to protocol conduct and/or individual subject safety. 

Responsible for gathering, reviewing, and providing preliminary assessments of medical surveillance events to the Study Clinical Scientist and the Study Medical Monitor. Generate study safety events trackers, periodic medical monitoring reports and safety reviews in line with the needs of the study. 

Participate in cross-functional study execution team activities relating to clinical data review.

Contribute to ICFs, training documents, and other clinical and regulatory documents 

Interact with internal and external stakeholders (study sites, vendors, etc.) in support of clinical trial objectives related to subject safety and clinical data monitoring; responds to or triages medical and safety-related questions for appropriate actions. 

Sponsor/CRO GCP experience required (~7-10+ years in a Clinical Project Manager or QA role is ideal) 

Very Strong English Language proficiency required (written and verbal)

Strong operational understanding of Clinical Trials and GCP

Very strong Project Management experience is a must – this person will be managing deliverables that depend on other people

Exemplary organization, communication, and meeting facilitation skills – this is critical. This person needs to be able to clearly articulate concepts both verbally and in writing and facilitate meetings efficiently.

Exemplary QC skills – this person needs to be detail oriented.

Life Sciences degree

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