Vacancy for Clinical Research Associate in Lonza
Lonza is one of the world's leading
suppliers to the pharmaceutical, healthcare and life science industries.
Products and services span its customers’ needs from research to final product
manufacture. It is the global leader in the production and support of chemical
and biological active pharmaceutical ingredients. Lonza is also the world
leader in microbial control providing innovative, chemistry-based and related
solutions to destroy or to selectively inhibit the growth of harmful
microorganisms. In addition, Lonza is a leader in cell-based research,
endotoxin detection and cell therapy manufacturing. Furthermore, the company is
a leading provider of value chemical and biotech ingredients to the nutrition
and agro markets.
Post: Clinical Research
Associate-000003HP
Primary
Role Responsibilities
1.· The CRA is expected to follow the policies, procedures, guidelines, and standards for excellence and professionalism established by LONZA.
· Additionally, this position will assure that all clinical and laboratory research activity adheres to policies, procedures and requirements.
· Preparation of Informed Consent Form (ICF), Case Report Form (CRF)
· Maintain on going communications with sites to provide information, queries resolutions,
· Follow and track clinical research milestones for assigned projects.
1.· The CRA is expected to follow the policies, procedures, guidelines, and standards for excellence and professionalism established by LONZA.
· Additionally, this position will assure that all clinical and laboratory research activity adheres to policies, procedures and requirements.
· Preparation of Informed Consent Form (ICF), Case Report Form (CRF)
· Maintain on going communications with sites to provide information, queries resolutions,
· Follow and track clinical research milestones for assigned projects.
2. Assist QA in
preparation and review of the Clinical operation SOPs and their associated
documents.
3. Performs other study related tasks as assigned by managers.
4. Training of the personal on site for tissue collection.
5. Maintain audit, SOP and training compliance.
3. Performs other study related tasks as assigned by managers.
4. Training of the personal on site for tissue collection.
5. Maintain audit, SOP and training compliance.
Candidate
Profile
Maintenance of quality systems and cGMP compliance for the business by ensuring that all team members comply with processes, procedures and instructions for all activities in which the team participates.
Maintenance of quality systems and cGMP compliance for the business by ensuring that all team members comply with processes, procedures and instructions for all activities in which the team participates.
Safety
Responsibility
· Is knowledgeable and complies with all pertinent safety policies, rules and regulations.
· Ensure that all team members comply with safety rules and regulations.
· Is knowledgeable and complies with all pertinent safety policies, rules and regulations.
· Ensure that all team members comply with safety rules and regulations.
Skill
Requirements
Biological background (Masters) or equivalent 2-3 years experience in clinical research. Demonstrates high level of Customer Relationship Management.
Biological background (Masters) or equivalent 2-3 years experience in clinical research. Demonstrates high level of Customer Relationship Management.
Additional
Information:
Location: Hyderabad
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: R&D
End Date: 10th May, 2014
Location: Hyderabad
Industry Type: Pharma/ Biotech/Clinical Research
Functional Area: R&D
End Date: 10th May, 2014
Labels: Clinical Research Associate, Clinical Research job, M. Pharma, M. Pharma jobs, M.Sc, Pharmaceutical jobs, Research Jobs, Research Jobs in india
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