Details of the Organization
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. They have over 28 years of proven high-quality delivery and results across all their services with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific. They are on a mission to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Join their passionate team and make a meaningful impact on global healthcare!
Details of the Job/Internship
ClinChoice is a global full-service CRO dedicated to professional development and providing an excellent work-life balance, with a quality-focused, collaborative “one-team” culture. They are looking for a dynamic person to join there in-house team as a Regulatory Operations Trainee on a permanent basis. You will work on projects from there varied client base, ranging from small to big pharmaceutical, biotechnology, medical device and consumer health companies.
Join there team: you can be part of making a difference in peoples’ lives and experience a fulfilling and rewarding career!
Role and Responsibilities
Main Job Tasks and Responsibilities:
- Responsible for the building, publishing, archiving activities and associated tasks for assigned regulatory submissions within agreed timelines.
- Adhering to quality procedures and standards related to submission publishing. Adhering to the appropriate use of document management systems, publishing and validation tools, through the use of working practices and quality control steps to ensure regulatory compliance.
- Support other team members with submission workload, when necessary, to provide flexible support for the submission portfolio.
- Support global/local teams by completing tasks assigned by submission coordinators Adhere to Pfizer compliance standards.
Eligibility
Education and Experience:
- Bachelor’s or Master’s Degree in Pharmacy or Life Sciences.
- Should possess good English language skills, both written & verbal.
- Should possess good interpersonal skills with excellent collaboration capabilities.
- Should be pro-active & initiative driven.
- Should be solution-centric in approach.
The Application Process:
Once you have submitted your CV, you will receive an acknowledgement that they received it. If you have the requirements they need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications they receive, they cannot reply to everyone individually if you are not successful.
Salary/Stipend
The salary will be discussed with the candidate itself.
Type of Opportunity
Fulltime
Country
India
State
Karnataka
City
Bengaluru
Address
Bengaluru, Karnataka