Govt Job @ CDSA | Salary of Rs. 75,000/- p.m.

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Freshers Pharma & Chemistry Associate Scientist Post @ Syngene

text-align: center;">CLINICAL DEVELOPMENT SERVICES AGENCY
An extra mural unit of THSTI,
Department of Biotechnology, Ministry of Science & Technology, Govt. of India
3rd Floor, THSTI Building, 3rd Milestone, Gurgaon-Faridabad Expressway, Faridabad –
121001 (Haryana)

Department of Biotechnology (DBT), Ministry of Science & Technology, Government of India launched CDSA on 28 September 2009 as an extramural unit of Translational Health Science & Technology Institute (THSTI). It was created to facilitate development of affordable healthcare products for public health diseases. Registered as a not-for profit research organization, it aims to develop an eco-system for training and learning and work with public sector institutions, and small and medium enterprises (SME) to translate innovative technologies into medical products for public good.

Job Title  Senior Research Officer (Zinc Sepsis Study)

Salary:  up to Rs. 75,000 per month, consolidated for 20 months

Job Description:

  • Oversees quality management processes and provides guidance and support to project teams to meet quality
    standards.
  • Advising and providing training to research team on interpretation of GCP/ethical requirements for quality
    management.
  • Overseeing and/or performing quality functions and executing quality programs (clinical operations,
    clinical laboratory, data management review)
  • Developing quality management plan and ensuring compliance
  • Ensure compliance with agreed upon documentation practices
  • Identifying areas of deficiency and trends in quality and escalating to appropriate personnel
  • Setting up documentation standards and ensure compliance throughout the study span
  • Collaborate with clinical and project management team to ensure compliance with quality standards,
    timelines and appropriate follow-up in areas of deficiency
  • Coordinate expert monitoring visit/ audits as per project requirement.
  • Educating, training, and mentoring research team in quality improvement methods
  • Supervise quality management team to ensure efficient clinical monitoring (site preparedness, study
    initiation, interim monitoring, close out & termination), archiving, reporting and follow-up for corrective and
    preventive action.
  • Travel up to 50%, as assigned
  • Quality assurance through external monitoring
  • Work with Clinical Portfolio Management and other internal departments on their requirements as and
    when required

Qualifications

  • Master’s degree in life sciences or biomedical sciences or pharmacy. At least 5 years of demonstrated experience in the area of Quality Control, Quality Assurance and Clinical operations. GCP/ GLP trained personnel will be preferred.
  • Good understanding of needs for project and job responsibilities.
  • Extensive knowledge of GCP/GLP and appropriate clinical research regulations and guidelines.
  • Ability to develop and implement clinical research monitoring plans, SOPs, database concepts, and
    formats
  • Ability to build effective project teams, ability to motivate others, delegation, drive and timely/ quality
    decision making Operational skills including focus and commitment to quality management and problem solving
  • Influencing skills including negotiation and teamwork.
  • Effective communication skills to provide timely and accurate information to stakeholders
  •  Ability to assess non-compliance situations and recognize potential or real wider strategic risk to
    project, escalates when needed.
  • Ability to identify systematic causes of complex quality problems and recommend long-term solutions
  • Fair and ethical. Creates a culture that fosters high standard of ethics.
  • Basic business computer skills (MS Word, Excel, e-mail)

General Terms and Conditions

1. All educational professional and technical qualification should be from a recognized Board/ University and full-time.
2. The experience requirement specified should be experience acquired after obtaining the minimum educational qualifications required for the post.
3. Persons working in Govt. or Public Sector undertaking should produce “No Objection Certificate” at the time of Interview.
4. The qualification, experience and other requirements for the post can be relaxed at the discretion of the controlling authority, in case candidates are otherwise well qualified.
Interested candidates may please send their current CV with a recent photo and cover letter indicating their motivation for the position applied for (150 words) and three references along with the attached datasheet and excel sheet posted in the website. E-mail should be submitted with subject line Application for the post of “Senior Research Officer” (Zinc Sepsis Study)” to [email protected].
5. Only shortlisted candidates will be contacted for further discussion
6. Incomplete applications will stand summarily rejected without assigning any reasons.
7. The salary is a consolidated sum as per sanctioned order without any other benefits. Salary mentioned against the position is an actual and will be based on experience, qualifications, skill set, etc. of the candidates.
8. This position is strictly project-based and hired only for 20 months.
9. All results will be published on our website and all future communications will be only through email
10.Candidates (Including SC/ST and other backward classes) are not entitled for the travel reimbursement or any other reimbursement.
11.This position will be placed in CDSA Faridabad office at NCR Biotech Science Cluster at Faridabad Gurgaon Expressway, Faridabad.
12.Canvassing in any form will be a disqualification.

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