Company Name:-
Teva Pharmaceuticals

Job Location:-
Bengaluru, Karnataka

Job Summary:-
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
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;
To familiarize with SOPs required for the function of independent monitor role
To acquire the monitoring skills across a range of therapeutic areas
In assistance with the project team/line manager, provide oversight of study-related in-house activities on assigned projects.

To accompany experienced monitors for in-depth, on-site monitoring experience (called as co-monitoring visit / co-site Initiation visit)
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 participate in the project meetings (in-house / sponsor facilitated) and also to prepare the minutes of such meetings.

Qualifications
2-4 years of experience in Clinical trials with B.

Pharma/ M.

Pharm/MSC-science background

Function
Research & Development
Sub Function
Clinica

FOR MORE DETAILS CLICK BELOW LINK [convertful id=”110657″]

Click Here For More Details