KEM Hospital Research Centre, Pune

K.E.M Hospital, Pune celebrated its diamond jubilee in 1972. At that time a need was felt to further improve and expand their services.Read Further

K E M Hospital Research Centre, Pune


Post of Junior Research Fellow & Medical Officer

On the event of the project entitled “Supplementation of vitamin B12 to improve B12-folate ratio in pregnancy and its effect on birth outcome”, conducted by “ICMR (Dept. of Health Sciences) a walk –in – interview has been scheduled at KEM Hospital Research Centre (TDH Building, 3rd floor), Rasta Peth, Pune on 09 /11  / 2016 at 12 noon. Eligible candidates are invited to attend the interview with educational & experience certificates, application and CV.


Educational Qualification

No. of Post

Junior Research Fellow

MSc. (Nutrition/ Chemistry/Biology)


Medical Officer

B.H.M.S. or  B.A.M.S.


K E M Hospital Research Centre, Pune

Post of a Project Manager

Is seeking a highly motivated and experienced Clinical Research Project Manager for growing organization for its various projects, trials, studies based at Vadu, Dist : Shirur.

Job Description

The PM will oversee several clinical trials. In this role he will manage large, complex, programs and mentor members of the project management team. He will take ownership of projects to assure proper planning, timely initiation/completion and high quality documentation. He will have a key coordination role with the Sponsor, vendors, sites, CRAs, Recruitment Management, Quality Assurance, & Data Management departments.

Responsibilities include, but are not limited to:

  • Manage the project(s) within the approved budgets and timelines. Develop detailed plans and prioritizes the tasks within the plan to achieve project goals.
  • Leverage resources, expertise, and knowledge across multiple projects to ensure attainment of project deliverables. Communicates with internal project team and sponsor project team.
  • Responsible for financial oversight of the study/program.
  • Participate in the selection and on boarding process for new clinical staff and Manage staff in accordance with organization’s policies and applicable regulations. 
  • Responsibilities include planning, assigning, and directing work; appraising performance and guiding professional development; rewarding and disciplining employees; addressing employee relations issues and resolving problems.
  • Utilizes project metrics and ensures staff understands their role, functional areas and takes ownership to drive results.
  • Ensures roles and responsibilities are clear across internal and external organizations to achieve desired results.
  • Coaches Managers, Assistant Managers, Clinical coordinators, and team members on appropriate communications methods. 
  • Conducts team meetings (prepares agenda and reviews minutes).
  • Plans and drives patient recruitment and retention
  • Serves as initial point of contact for all clinical management and other functional areas,
  • Ensures effective communication plans are in place for the clinical team and are auctioned.
  • Monitors the preparation and timely completion actions and ensures effective follow up and resolution of site issues.
  • Oversees communication of escalated issues Sponsor  and provides escalation path for the team
  • Performs any other duties required to ensure the success of the clinical trial project.
  • Assures that staff works in compliance with all established processes and SOPs.
  • Directs and manages staff including, training, mentoring, and performance management.
  • Miscellaneous duties, as necessary, in support of Project Management initiatives and business priorities and objectives.

Skills & Requirements

Ideal candidate will have.

  • MBBS/BAMS degree or Master in Pharmacy
  • at least 6-7 years of relevant project management experience at Site, CRO and/or pharmaceutical industry
  • Strong experience in clinical trial operation and management
  • Experience in managing complex or global trials
  • Budget/finance experience on a project level and demonstrates a full understanding of project financials
  •  Ideal candidate will have Vaccine experience.

Must possess detailed  knowledge of DCGI regulations and GCP/ICH guidelines as they apply to the conduct of clinical research.

Excellent written and verbal communication skills in order to effectively communicate to a wide variety of audiences, including senior management/Sponsor/CRO.

 Strong computer proficiency with the MS Office Suite is required. 

 We offer a competitive compensation package for full time employees, commensurate with background and experience.