Vacancy for post of Site Incharge in CLINI INDIA - Require B.Pharm/M.Pharma

CLINI INDIA founded 2009 is a progressive and premier academy in clinical research that has rapidly gaining a good reputation for excellence through its innovative approach in clinical research. Clini India is an academy with a good reputation in clinical research industry. Clini India is a premier institution of CR education in clinical research domain.Clini India delivers Full time, Part time and e- learning training in Clinical research education.

Post: Site Incharge

Job Description:
The post holder will have the leading role in planning, coordinating and completing the projects. Responsible for Documentations at the sight. He should have excellent communication and presentation skills together with the ability to organise and motivate others. Supervise CRC’s and their day to day work. Previous experience in the management and coordination of clinical trials is desirable but not essential;

Responsibilities:
-The overall efficient day-to-day management of the trial.
-Recruitment, retention, training, appraisal and supervision of trial team members.
-Establishment of procedures to ensure adherence to trial protocols and administrative requirements.
-Ensuring the timely recruitment of trial participants with secure randomisation processes and subsequent efficient and effective data management.
-Monitoring the trial progress to ensure compliance with and adherence to the project plan and to identify, evaluate and rectify problems.
-Act as the point of contact for all external and internal agencies.
-Understand the requirements of the various controlling bodies, agencies and frameworks, guiding the project in conforming to those requirements and co-ordinating any necessary audit processes.
-Liaison with the Trials Steering Committee and Data Monitoring and Ethics -Committee with a particular view on compliance with Research Governance, Good -Clinical Practice, Data Protection and Ethical Requirements.
-Work with the Chief 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.
-Creation and maintenance of all trial files, including the trial master file, and oversight of site files.
-Assurance that personal and confidential information is restricted to those entitled to know.

Candidate Profile:
Qualification:
B.Pharm/M.Pharma with 2.5 years to 4 years of experience.
Salary : 15000K – 20000K

Additional Information:
Experience: 2 - 4 Years
Qualification: B.Pharm, M.Pharm
Location: Hyderabad
Industry Type: Pharma/ Biotech/Clinical Research
Division: Pharma