Alke Research private limited
http://www.AlkeResearch.comFounded :
2020
Type :
Services
Size :
20-100
Stage :
Bootstrapped
About
We are the fastest growing Contract Research Organisation in India. We have a healthy pipeline of projects and a very energetic management. We believe in human values and treat our employees as family. Our goals and objectives can be achieved together and the employee can be assured of a steady career growth in return of their efficient services.
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Jobs at Alke Research private limited
at Alke Research private limited
1 recruiter
Posted by ALBEN Sigamani
The recruiter has not been active on this job recently. You may apply but please expect a delayed response.
Remote, Bengaluru (Bangalore), Mumbai, NCR (Delhi | Gurgaon | Noida)
1 - 3 yrs
₹5L - ₹10L / yr
Project Management
Delivery Management
Good Clinical Practice
Monitoring
Business Development
+5 more
Senior Level CRA will be involved in project planning, commissioning and execution. Has to oversee project delivery timelines and lead the team members in faster, efficient and effective project execution. Should take the initiative for finding new clients and doing busines development.
At our organisation, the individual can expect to grow in their career to VP position and establish off shore units in 1 - 2 years
At our organisation, the individual can expect to grow in their career to VP position and establish off shore units in 1 - 2 years
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The recruiter has not been active on this job recently. You may apply but please expect a delayed response.
Remote, Bengaluru (Bangalore)
1 - 5 yrs
₹4L - ₹9L / yr
Good Clinical Practice
Clinical Research
Pharmacology
Regulatory affairs
CLINICAL TRIALS
+1 more
A full time Clinical Research Associate works on clinical trials and other exploratory research projects subcontracted by Alke Research Pvt Ltd. The job requires vibrant and hardworking individuals with a zeal to build a career in the clinical research industry.
Carry out independent site feasibility and selections
Help with site initiation and trial activation
Carry out independent site monitoring; online and offline
Help with preparing Serious Adverse Event report filing with the regulatory
Provide assitance to site in protocol related queries, ICH GCP Training for site personnel
Be a liasion between the sponsor, investigator and CRO
Support the site prepare and face regulatory audit / site inspections
Carry out independent site feasibility and selections
Help with site initiation and trial activation
Carry out independent site monitoring; online and offline
Help with preparing Serious Adverse Event report filing with the regulatory
Provide assitance to site in protocol related queries, ICH GCP Training for site personnel
Be a liasion between the sponsor, investigator and CRO
Support the site prepare and face regulatory audit / site inspections
Read more
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