Project Manager – Drug Safety Job in India

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Project Manager – Drug Safety Job in India

Location: Mysore, India

Essential Duties and Responsibilities:

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As a Project Manager

Supervision and coordination of following activities:

Lead and manage the project to comply with the SOW and SLAs.

Supervise all project related activities.

Single point of contact between the team and the client for smooth functioning of the project.

Communicate between the management and the team.

Record, maintain and track the metrics for both team members and project performance.

Review and evaluate AE case information to determine required action based on and following internal policies and procedures.

Process current incoming cases in order to meet timelines.

Provide guidance for Data entry.

Following up with sites regarding outstanding queries.

Follow-up on reconciliation discrepancies.

Follow departmental AE workflow procedures.

Train and mentor new team members as per requirements of the project.

Act as a management level liaison between Client and Bioclinica Project team.

Coordinate and manage administrative project issues.

Delegate tasks and responsibilities to appropriate personnel.

Identify and resolve issues and conflicts within the project team.

Recruit, select and train team members
Act as guide, coach and counselor for the team.

Other responsibilities:

Following up with sites regarding outstanding queries and reconciliation of discrepancies.

Closure and deletion of cases

Follow departmental AE workflow procedures

Oversee, mentor and guide the activities of the Drug Safety and Senior Drug Safety Associates.

High level of proficiency at all workflow tasks

Perform any other drug safety related activities as assigned.

Specialized knowledge and skills:

Subject Matter Expertise in Safety database
Proven experience in customer handling and relationship.

Proven ability to perform task management.

Proven People management skills.

Must have good presentation skills and the ability to give presentations.

Knowledge of the Life Sciences Industry a plus.

Experience in entire drug development life cycle.

Relevant product and industry knowledge

Experience with relevant safety databases and software applications

Communication skills:

Requires a proactive approach and excellent written/oral communication and interpersonal skills.

Strong interpersonal skills required to interact with clients, management, and peers effectively.

Effective cross-department communication.

Ability to document and communicate problem/resolution and information/action plans.

Technical skills:

Person should be familiar with MS Office tools/Data base and other applicable software.

Ability to educate/ train the team members as needed.

Contributing to the ongoing enhancement of Pharmacovigilance process and SOP’s including internal and external training.

Maintaining Pharmacovigilance systems including global safety database.

Other skills:

The ability to contribute to a team environment with a high degree of professionalism and skill. Demonstrated flexibility within a dynamic, fast-paced, cross-functional team. Demonstrated ability to complete multiple tasks concurrently and deliver results in a fast-paced environment.

Ability to perform under stringent timelines. working conditions: Normal office environment.

Compliance:

Awareness of organizational policies & procedures governing his/her job responsibilities. Awareness and compliance of QMS & ISMS policies & procedures and their impact at his/her job level. Should understand escalation matrix and escalate to the next level whenever incidents happen which are not in compliance with organizational, QMS & ISMS policies and procedures.

Working Conditions: Normal office environment.

Hours: Standard Hours 40 hours per week, one hour lunch, Monday – Friday. Additional hours as needed.

Willing to work in shifts as and when needed

 

Apply Here

 

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