Project Manager - Clinical Trials
Ecron
Acunova is a CRO combining the strengths from four previously
independent expert CROs on two continents serving established clinical research geographies of Europe, India and South East Asia (SEA). This integration enabled the four expert CRO’s to increase the value to sponsors with patient recruitment in India, SEA, Nordic countries, West Europe and East Europe with faster patient enrolment in clinical trials and timely database lock. It added services of early development and central lab. It enabled global delivery
of data and safety services. Ecron Acunova brings regional knowledge,
special therapeutic expertise, and integration resulting in high
performance, addressing sponsor’s needs for speed, cost, quality and
personalized service.
Post: Project Manager - Clinical Trials
Job Description:
• Managing and controlling quality of the execution of clinical protocol for a number of clinical trials at multiple sites, ensuring compliance with all regulatory and contractual requirements.
• To design and monitor clinical trials and user studies. Documentation and regulatory submissions
• The person shall be responsible for Clinical Trail site selection, investigator selection, designing of clinical trial including protocol preparation and all related work in compliance with GCP guidelines.
• Conducting international/global trials.
• Participating in protocol development, site/investigator selection, study initiation and termination activities.
• Developing and completing final study reports.
• Minimum 2 years of Project management experience is essential.
• Managing and controlling quality of the execution of clinical protocol for a number of clinical trials at multiple sites, ensuring compliance with all regulatory and contractual requirements.
• To design and monitor clinical trials and user studies. Documentation and regulatory submissions
• The person shall be responsible for Clinical Trail site selection, investigator selection, designing of clinical trial including protocol preparation and all related work in compliance with GCP guidelines.
• Conducting international/global trials.
• Participating in protocol development, site/investigator selection, study initiation and termination activities.
• Developing and completing final study reports.
• Minimum 2 years of Project management experience is essential.
Candidate Profile:
• Have 3-5 years experience in a recognized CRO / Pharmaceutical industry
• Having faced audit.
• Experienced in conducting global trials.
• Ability to create, manage and motivate a team of people.
• Ability to train the junior CRAs in various aspects related to clinical trials.
• Strict adherence to GLP, ICH & other Regulatory requirement.
• Monitoring the conduct and progress of the studies as well to ensure compliance with established protocols, appropriate research methodology, and study timelines.
• Have 3-5 years experience in a recognized CRO / Pharmaceutical industry
• Having faced audit.
• Experienced in conducting global trials.
• Ability to create, manage and motivate a team of people.
• Ability to train the junior CRAs in various aspects related to clinical trials.
• Strict adherence to GLP, ICH & other Regulatory requirement.
• Monitoring the conduct and progress of the studies as well to ensure compliance with established protocols, appropriate research methodology, and study timelines.
Additional Information:
Experience: 3-5 Years
Location: Bangalore
Education: B.Pharm, M.Pharm, B.Sc, M.Sc
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: CR
End Date: 30th Sept., 2011
Experience: 3-5 Years
Location: Bangalore
Education: B.Pharm, M.Pharm, B.Sc, M.Sc
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: CR
End Date: 30th Sept., 2011
Forward Your Resume at, careers@ecronacunova.com
posted by National College Of Pharmacy @ 01:35
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