Teva Pharmaceuticals Hiring R&D Intern BPharm + PG Diploma Clinical Research / M.Pharm Apply Now
Company
Info
Teva
is a global pharmaceutical leader and the world's largest generic medicines
producer, committed to improving health and increasing access to quality health
solutions worldwide. Our employees are at the core of our success, with
colleagues in over 80 countries delivering the world's largest medicine cabinet
to 200 million people every day. We offer a uniquely diverse portfolio of
products and solutions for patients and we've built a promising pipeline
centered around our core therapeutic areas.
We are continually developing patient-centric solutions and
significantly growing both our generic and specialty medicines business through
investment in research and development, marketing, business development and
innovation. This is how we improve health and enable people to live better,
healthier lives. Join us on our journey of growth!
Job
Description
In
assistance with the project team/line manager, provide oversight of
study-related in-house activities on assigned projects.
Assist
Project team in the in-house filing of study related documents.
Assisting
the study team to collect and compile essential documents required for the
smooth initiation of study sites.
Assisting
the study team in the compilation of the regulatory dossiers to be submitted to
the regulatory bodies (i.e. DCGI) and/or Institutional / Independent Ethic
Review Board(s) for grant of permission to conduct the clinical study.
Under
the guidance of the Project Manager / Study Team for the project, to familiarize
with data query resolution process within timelines.
To
assist the study team in vendor management as well as follow up with
Investigator(s) site on assigned project(s).
To
perform other duties assigned by Line Manager / Project Manager for the project
and/or for other departmental activities.
To
participate in the project meetings (in-house / sponsor facilitated) and also
to prepare the minutes of such meetings.
To
undergo other responsibilities as and when assigned by the management.
Sub
Function
Drug
Development and Preclinical Studies
Qualifications
Qualification
: BPharm + PG Diploma Clinical Research / MPharm (Pharmacology)
Experience
: 6months - 1yr.
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