Life Sciences Associate Project Specialist Job at Pfizer

Life Sciences Associate Project Specialist Job at Pfizer

Life Sciences Associate Project Specialist Job at Pfizer. Pfizer is hiring candidates for the Associate Project Specialist vacancy. Interested and eligible applicants can check out all of the details on the same below:

Job Title: Associate Project Specialist

Job ID: R2616196

Location of Pfizer Vacancy: Hyderabad

Mission statements –

• Responsible for project management support to the Scientific Writer ensuring the end-to-end effective project delivery of the designated publication/medical education deliverable across all phases
• Initiate submission (as required), amend submission based on comments (as required)
• Support the Writer with the development of a scope of work; Build plan and schedule for agreement with the internal customers
• Arranging key internal(GBUs, Medical Leads) and external customer (Authors/Investigators )meetings. Tracking of the delivery of activities (including managing issues and risks) and supporting follow-ups.
• Supporting required submission, compliance and approval activities, and ensuring compliance with publication processes and use of publication management tools.
• Supports the management of the assigned publication or medical education in line with the agreed budget. Supporting and managing as required external spend tracking (e.g. approvals, purchase orders, goods received)
• Supports adherence to associated compliance-related activities and approvals (with the internal customer taking accountability for compliance).
• Updates as required with approval/compliance tools (e.g. PromoMats, NAYA,..)
• Manage end to end the process through Datavision, Matrix, Promomomats, Naya or any contracting database.

Collaboration –

• Scientific communication global or local teams
• Medical content enhancement teams

People –

• Maintain effective relationships with the end stakeholders (Medical scientific community) with an end objective to develop education and communication content as per requirement
• Actively leads and develop MedHub operations activities
• Ensure new technologies are leveraged

Performance –

• Ensure publication materials (Slide decks, Abstract, poster, manuscript) are delivered, stored as per agreed timelines and quality
• Develop tools, technology and process in order to constantly improve quality and productivity.

Process –

• Support delivery of projects in terms of resourcing, quality, timeliness, efficiency, and high technical standards for deliveries made by the medical writing group, including scientific documents and clinical/medical reports
• Contribute to overall quality enhancement by ensuring high scientific standards for the output produced by the medical writing group
• Secure adherence to compliance procedures and internal/operational risk controls in accordance with any and all applicable regulatory standards

Knowledge, Skills & Competencies / Language –

Therapy Area Specific

Diabetes
Familial hypercholesterolemia
Cardiovascular disease
Multiple sclerosis,
Immunology
Oncology
Market access
Emerging markets
Generics
Vaccines
Vitamins and supplements
Digestive
Allergies
Parkinson
Haemophilia
Rare diseases
Rare blood diseases

Writing/communications skills –

• Scientific writing/comms.
• Medical writing/comms.
• Publication planning
• Stakeholder management
• Project management

Qualifications – Graduate / Post Graduate degree in life science is a must.

Requirements of the job –

• Project Management experience in pharmaceuticals of up to 2.5 years is preferred.
• Medical communication/pharma experience desirable.

Apply Online

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