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Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development, and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical industries around the world.
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Syngene’ s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA, and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation.
Position: Junior Manager – Project Management (Clinical Development)
Location: Bangalore, Karnataka, India
Department:Â Global Program Management
Job Description:
Job Purpose: This role requires the incumbent to support the Project Manager in coordinating the Human Pharmacology Unit (HPU) projects.
Key Responsibilities:Â
- Track project plan with respect to resource, schedule, and budget. Monitor progress of project activities and deliver timely updates to the Project Management Office (PMO) and management.
- Liaise with the functional departments/sponsors to develop detailed project plans, resources, budgets, task management log to achieve project objectives and deliverables.
- Lead and schedule team meetings, preparation of agendas, and circulate minutes. Prepare and present project information at internal and external meetings.
- Identify and manage (with the project team leader) all project-related issues, to ensure prompt resolution and to avoid negative impact on budget or schedule
- Manage project budget and revenue (along with Project Leads).
- Map resources to project in SAP.
- Liaise with Finance/ Business Development team to ensure appropriate revenue recognition and timely and accurate invoicing.
- Follow environment, health, and safety (EHS) requirements at all times in the workplace ensuring individual and lab/plant safety
- Attend training on environment, health, and safety (EHS) measures imparted company
Technical/Functional Skills:
- Â Identifies the steps involved in Bioavailability/Bioequivalence (BA/BE) studies and in clinical trials
- Should have involved in the direct handling of clinical studies in a well-defined project management role
- Understands project management and its steps in clinical research studies
- Understands budgeting and should have a penchant for financial aspects of clinical research studies
- MS Excel, Word, and Powerpoint at a proficient level of expertise is a requirement.
- Data Analysis skills, statistical knowledge is an added advantage.
Behavioral Skills:
- A team player, relational personality with patience and understanding
- Displays and practices positive attitude towards a difficult situation and be empathetic
- Excellent communication skills
- Displays and practices honesty, integrity, and professionalism
Qualification: Graduate/Masters in Life Science discipline, Basic project management training or certification is an added advantage
Experience: An experience of minimum of 5 years in a Clinical Research Organization (CRO) or Pharmaceutical company.
Contact Details:
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