Career for candidates with Degree or diploma in clinical research for Reflexology Study in CDSA

Clinical Development Services Agency (CDSA) has therefore been formed as a not-for-profit society to provide supportive and focused environment to host world class clinical translation through a collaborative network of clinical investigators and premier research institutions. It will tend enterprises, particularly SMEs involved in new technology innovation, to facilitate translation of scientific know-how into viable products for public health diseases like malaria, tuberculosis and dengue among others.

Post: Program Officer for Reflexology Study

Skills:

Experience in planning, coordinating and completing the project.
Excellent communication and presentation skills, together with the ability to organize and motivate others.
Demonstrate flair, enthusiasm, innovation and leadership when faced with challenges and will provide strategic, tactical and operational management skills in the planning and execution of the project

Experience:

2-3 years’ experience in managing and coordinating clinical studies, including drug trials and/or epidemiological studies

Job profile:

Overall efficient day-to-day management of the study.
Establishment of procedures to ensure adherence to trial protocols and administrative requirements.
Monitoring the trial progress to ensure compliance with and adherence to the project plan and to identify, evaluate and rectify problems.
Management of the trial budget(s) and maintenance of the accounts.
Act as the point of contact for all external and internal agencies.
Provision of regular and ad hoc information, both written and verbal, to all the Advisory/Committee members, to include reports, updates and guidance.
Work with the Coordinating Investigator to ensure that the trial is meeting its targets, is producing meaningful output and to predict and plan any changes that warrant requests to changes in protocol, funding or time.
Planning and supporting the meetings and work of the various groups and bodies associated with the trial.
Creation and maintenance of all trial files, including the trial master file, and oversight of site files.

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GENERAL TERMS & CONDITIONS:

All educational professional and technical qualification should be from a recognized Board/ University and full-time.
The experience requirement specified should be experience acquired after obtaining the minimum educational qualifications required for the post.
Persons working in Govt. or Public Sector undertaking should produce “No Objection Certificate” at the time of Interview.
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 appear for the walk-in-interview on December 17, 2013 at CDSA, Gurgaon. For complete address please logon at cdsaindia.in/contact-us
The salary is a consolidated sum without any other benefits.
This position is strictly project-based only.
This position will be filled as per the need and availability of suitable candidates.
Canvassing in any form will be a disqualification.

Additional Information:
Location: Gurgaon
Experience: 2-3 yrs
Emoluments: Rs.35,000 per month, consolidated
Essential qualification: Post graduate degree in life sciences
Desirable qualification: Degree or diploma in clinical research.
Industry Type: Pharma/ Biotech/Clinical Research
Employment Type: Full Time
Job Type: Regular
Walk in Date: 17^th Dec., 2013

CLINICAL DEVELOPMENT SERVICES AGENCY
An extra mural unit of Translational Health Science & Technology Institute
Department of Biotechnology, Ministry of Science & Technology, Govt. of India
470 Udyog Vihar, Phase III, Gurgaon 122016

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