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Junior Manager - Project Management (Clinical Development)

5.00 to 10.00 Years   Delhi   26 Jul, 2022
Sygene
Job LocationDelhi
EducationNot Mentioned
SalaryNot Disclosed
IndustryPharma / Biotech
Functional AreaBio Tech / R&D / Scientist
EmploymentTypeFull-time

Job Description

    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 companyEducational Qualification: Graduate/Masters in Life Science discipline Basic project management training or certification is an added advantageTechnical/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 it s 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.Experience: 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 professionalismEqual 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.,

Keyskills :
sapmechanicalsafetyproject management officecommissioningtroubleshootingequal employment opportunityproject management training

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