Global Project Management

Cliantha Research

1 - 2 years

2 - 3 Lacs

Ahmedabad

Posted:5 hours ago| Platform:

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Skills Required

BABE Studies BABE Clinical Research Clinical Operations GLP Clinical Trials

Work Mode

Work from Office

Job Type

Full Time

Job Description

Role & responsibilities:

Responsible for creating, coordinating and maintaining the Master Study Schedule for all Cliantha sites.
Working with all Head of Departments (HODs) of Cliantha Research on a regular basis to ensure the relevant project milestones are discussed and needs of Sponsor and functional areas are not compromised.
Create, plan and monitor all project activities in PM database ensuring accuracy at all times.
Responsible for identifying interdependencies for all projects and facilitate communication among functional areas where required.
Understands time-sensitive nature of critical path project activities and notifies the relevant teams, and/or management of related issues.
Works with management to establish project interim milestones and ensures projects are on schedule to ensure our report structure/compilation is communicated and assist where required, i.e. CS-BE , FDA tables

Preferred candidate profile

The candidate must have experience in BA/BE Studies with excellent English communication (Mandatory)

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