Warning: Undefined array key "rcommentid" in /customers/6/5/f/pcm.me/httpd.www/wp-content/plugins/wp-recaptcha/recaptcha.php on line 348 Warning: Undefined array key "rchash" in /customers/6/5/f/pcm.me/httpd.www/wp-content/plugins/wp-recaptcha/recaptcha.php on line 349
Warning: Undefined array key "direction" in /customers/6/5/f/pcm.me/httpd.www/wp-content/themes/linepress-2.8/single-vacancy.php on line 4 Warning: Trying to access array offset on value of type null in /customers/6/5/f/pcm.me/httpd.www/wp-content/themes/linepress-2.8/single-vacancy.php on line 4

Medical science liason

Submitted:
10 years
ago
Direction :

Submitted In:

Vacancy   :

The candidate will be responsible for company’s medical affairs tasks assigned by medical advisor/ manager to include medical information, medical training, clinical trials and drug safety. he will ensure that the company’s high standard is maintained as far as medical related issues to the company products are concerned and will maintain close contact with opinion physicians and medical departments of government institutions.

Duties & Responsibilities

Responsible for answering medical queries from the Field.Assists Product Managers to answer medical questions from authorities and generate public where appropriate.Maintenance of file copies of all promotional mailings, advertisements, slides, sales aid, gadgets and other material prepared and medically cleared according to IFPMA and local authorities’ guidelines.Identify and maintain strong scientific partnerships / business relationship with scientific leaders (SLs).Interact with SLs across entire range of potential interaction (lectures, congresses, research…etc)Provide SLs with various scientific updates e.g. new mechanisms of action, introduce new chemical entities with emphasis on Company pipe lineSupport sales and marketing teams through providing regular scientific updates and training sessions.Speakers’ management along with sales and marketing collaboration.Conduct presentations to HCPs using company approved slide setsAssist in preparation of protocols, trial drug logistics and the monitoring of the trials according to the required company and GCP standards and to the agreed budget and time table.Study proposal and recommended investigators given by the Product Manager of relevant product.Responsible for follow-up of clinical trials.Give advice and support to investigators running trials in order to optimize the quality of the proposed study.Ensure that guidelines on drug safety and adverse event reporting are in compliance with the company guidelines.Support SLs in developing Clinical Practice Guidelines

ESSENTIAL REQUIREMENTS

·         Should be physician with Two years experience in pharmaceutical/medical environment is preferred

·         Fluent and confident in English and computer literate

·         Strong presentation and communication skills.

Send CV to
Msljob04@gmail.com

Share This:
«

»
add Add a job vacancy