MITOCON BIOPHARMA PVT LTD

Huge openings Mitocon Biopharma pvt ltd

1. MEDICAL INFORMATION CONTACT CENTER

Designation: Assistant Manager/DSA-III

Experience: 5-6yrs

Qualification: Pharma D/Bpharma/Mpharma

Managing the team members in delivering the daily activities .

Adopting any delegation and use of project assurance roles within agreed reporting structures.

Application of appropriate technical, quality strategies and standards to deliver the activities as per client requirements.

Monitoring overall progress of all the projects and utilization of resources appropriately.

Regular planning and monitoring of the projects and intimate to senior management if there are any escalations.

Support in writing activities-standard operating procedures, work instructions and process related documents.

Determining the root cause analysis for deviations any proposing appropriate CAPA.

2.FRESHER

Location: Begumpet, Hyderabad

Experience:0-0yrs

Qualification: Bpharma/Mpharma/Pharma D

Should be interested for "NIGHT SHIFT"

Excellent Communication skills.

"BIKE MANDATORY:

·          Medical enquiry handling through verbal telephone and written enquiries from Healthcare Professionals (HCPs) / patients, other people and Consumers about the medical products.

·          Receive information or inquiry through phone call/email/fax/mail & Generate reports and create a record in Track Wise in AWS.

·          Ensure that all the calls are getting populated in AWS.

·          Enter all the relevant information received through phone calls/email/fax/mail into AWS Log.

3. MEDICAL REVIEWER

Location: Begumpet, Hyderabad

Qualification: #BDS #MDS #MBBS

Experience: 1-5yrs(Pharmacovigilance)

Perform ICSRs medical assessment, including the determination of seriousness, expectedness/listedness/Labeledness, and causality of adverse events in compliance with current regulations, internal and external guidance documents, Standard Operating Procedures, Safety Job Aids, User Reference Guide and case processing/coding conventions.

Determine regulatory reportability of cases obtained from literature, clinical trials, spontaneous and solicited reports within assigned therapeutic team and across all products/sites, as necessary, and in a timely fashion.

Maintain the timely submission of expedited reports. Support different Therapeutic Areas for case processing and submission within timelines.

4.ASSISTANT MANAGER- Aggregate reporting(RMP)

Experience: 4-5yrs in aggregate reporting.

Location: Hyderabad

Designation: Assistant Manager

Prepare periodic safety reports on products that are in development (DSUR, IND Annual Report) or that have been granted regulatory approval (PADERs, PSURs and PBRERs, Signals etc.).

To generate ICSRs and Product complaints line listings as per the project requirement.

interested candidates kindly call on 9154383165call timings 10:00a.m to 06:00p.m(No Calls on Saturdays and Sundays) or share your resume to hr@mitoconbiopharma.com

Contact person: 

Assistant Manager-HR