Project Manager

Safeguard Global Recruiting; India; On-site; INR 1,200,000 - 1,800,000; Full time

Job summary

Safeguard Global Recruiting seeks an experienced project manager to ensure successful delivery of clinical trial projects. You will work with the Global Project Management Head, PM Team, and Study Team to apply project management principles and established methodologies across programmes of work.

The role requires 3-5 years in the industry with at least 1 year in PM roles within a CRO, pharma, or biotech setting, and strong knowledge of drug development, regulatory and ICH GCP guidelines, plus

Qualifications

• 3-5 years industry experience including at least 1 year in Project Management roles in clinical trials within a CRO, pharmaceutical or biotech setting.
• Good knowledge of the drug development process, regulatory and ICH GCP guidelines and their application to clinical trials.
• Detailed and proactive approach to risk and issue management.
• Good time management skills for working within a fast-paced environment.

Responsibilities

• The ideal candidate will be working with the Head of Global Project Management, Project Management Team and Study Team to ensure the successful delivery of assigned projects or programmes of work, by application of project management principles and implementation of project management methodologies and processes.

Skills

Project management

Clinical trials

Risk management

Time management

Education

Life science degree

Job description

The ideal candidate will be Working with the Head of Global Project Management, Project Management Team and Study Team to ensure the successful delivery of assigned projects or programmes of work, by application of project management principles and implementation of project management methodologies and processes.

Responsibilities

• 3-5 years industry experience including at least 1 year in Project Management roles in clinical trials within a CRO, pharmaceutical or biotech setting.
• Good knowledge of the drug development process, associated regulatory and ICH GCP guidelines and their application to clinical trials.
• Detailed and proactive approach to risk and issue management.
• Good time management skills for working within a fast-paced environment.

Qualifications

• Degree or similar related life science qualification or equivalent combination of education and experience.