Junior Manager - Project Management (Clinical Development) - [B863]

Junior Manager - Project Management (Clinical Development) - [B863]

13 Nov
Syngene International Ltd

13 Nov

Syngene International Ltd


Job Description


Designation: Junior Manager Project Management

Job Location: Bangalore

Department: Global Program Management

About Syngene

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. 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.

Job Purpose: This role requires incumbent to support 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

Educational Qualification:

Graduate/Masters in Life Science discipline

Basic project management training or certification is an added advantage

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 penchant for financial aspects of clinical research studies

MS Excel, Word and Power point at proficient level of expertise is a requirement.

Data Analysis skills, statistical knowledge is an added advantage.


An experience of minimum 5 years in Clinical Research Organization (CRO) or Pharmaceutical company.

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

Equal Opportunity Employer:

It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.

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