• Responsible for providing the sales team with the necessary technical expertise to enable them to sell the product. This involves printed and electronic promotional material, product training, and relevant clinical papers.• Responsible for reviewing product data to ensure that the field force is kept up to date on new developments regarding the companies or competitors products.• Act as point of first reference for all product related enquiries and work collaboratively with colleagues in Clinical Research and Regulatory to address any issues that may arise.• Close liaison with the field force to assess the response to and suitability of current promotional material and to ensure that the printed promotional material is being used optimally.• Design market research projects to assess customer attitudes to the current product range and new product introductions. Either conduct this research with in-house staff or manage an outside agency ie initial identification of suitable partner, definition of responsibilities, communication plan, divisions of responsibility, milestones, contract with company, review transcripts and reports, and recommend action plans from the research.• Assist with the development of the annual marketing plan and for controlling advertising, promotion and sales aids in accordance with the annual marketing plan.• Responsible for preparing product forecasts, and constantly monitoring inventory levels including liaison with production to ensure supply timelines.• Liaise with the advertising agency regarding the product campaign including journal advertising, direct mail and conferences.

Assisting in dossier filing and preparation for Pharma and Nutraceutical products. Assisting BD in molecule identification and analysis.

-Clinical study monitoring-Discuss any significant findings/issues, including those related to subject safety and those that could impact the over all integrity or progress of the study with relevant members of study team.-Ensures any further action required to complete records and address follow-up questions on SAEs, pregnancies and medical device incidents.-Ensure all completed CRFs/DQs are submitted to the designated data management centre according to study specific monitoring plan.-Updates or arranges update of the appropriate tracking system(s) to reflect study progress.-Prepares monitoring visit report.-Visit site(Hospital) for Source Document Verification(SDV).

4 Weeks Internship In Production & QAD Dept. In Abbott Laboratories (Pakistan) Landhi Plant.-Tablet manufacturing-Semi Solid Manufacturing -Liquid manufacturing -Validation Protocol-Sop's-In-Process analysis-GMP Regulations