Product Management Specialist

Position Summary / Objective

• To coordinate and author documents needed for marketing, ensuring the coordination and integration of the scientific, medical, and regulatory input from cross-functional team members.

Position Responsibilities

• 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.
• Responsible for providing product details to the Website Developer team for Export Client.
• Design market research projects to assess customer attitudes to the current product range and new product introductions.
• Assist with the development of the annual marketing plan and for controlling advertising, promotion and sales aids in accordance with the annual marketing plan.
• Provide Product Training, handling product related questions. Providing with the Launch Material.
• Responsible for Product launch activities to support the distribution partner.
• Compilation of product pitch decks for new business development.
• Coordination with Export Client for Product related information and Artworks.
• Participate in relevant document sub team(s) and ensure effective planning and management of timelines for all components of assigned documents.
• Participate in document strategy sessions, including messaging, document flow, logic, and consistency for assigned projects.
• Maintain document prototypes and shells.
• Comply with internal and external processes and guidelines while managing the review process and, on an ongoing basis, resolve issues, errors, or inconsistencies with pertinent team members to ensure timely completion and high quality of assigned documents.
• Review and edit documents as required.

Degree Requirements

• PharmD/PhD or Master's/Bachelor's degree with prior experience

Experience Requirements

• PharmD/PhD in a relevant scientific discipline or Master's/Bachelor's degree with approximately 2-4 years of regulatory documentation. All PhD in biological sciences and PharmD candidates are considered.

Key Competency Requirements

• Demonstrated strong writing skills in authoring and managing the production of marketing collaterals, Labelling, Detailing aids etc.
• Ability to analyze and interpret complex data from a broad range of scientific disciplines.
• Demonstrated ability to manage timelines and quality of work using strong organizational, communication, facilitation, and interpersonal skills in a cross-functional team.
• Working knowledge of a document management system and basic knowledge of the document publishing process.