HomeProductionJunior Manager Project Management | Clinical Development | Syngene International | Bengaluru

Junior Manager Project Management | Clinical Development | Syngene International | Bengaluru


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: 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: 

  • 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:

  •  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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