Biocon hiring Product Specialist - Gastro -"A"

Job Description

To attain or exceed the targeted sales volume in the assigned territory.
To do RTM/CME/Camps with paramedics or doctors.
To develop relations with the select doctors in the assigned territory.
Ensuring liquidation of stocks
To implement HO strategies on the field.
To provide regular feedback on competitor activity through market survey/ field interaction to the HO.

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Medical coding jobs "A"

Job Description

Dear Candidate,

Greetings!

Urgent Opening for Experienced Medical Coder - HCC Coding

Job Description  :- 

1. Any life Science graduate (Should be certified).

2. Should have minimum experience of 1 year in HCC coding.

3. Understand the client requirements and specifications of the project.

4. Ensure that the deliverables to the client adhere to the quality standards.

5. Immediate joinee will be an added advantage.

Interested candidates can directly walk-in to e4e office in Chennai  or send me the updated resume to the mentioned ID.

Timings: 11 am - 05 pm

Job Location :- Chennai

Contact Person :-Sowmithry Devi Jayakumar

Venue :- 

e4e Healthcare Business Services Pvt Ltd
Unit 1-5-2, Block A (the Eastern Front Wing)
TECCI Park No:285, Old Mahabalipuram Road,
Sholinganallur, Chennai - 600 119

Contact :  8754444001

Email :- sowmithrydevi.jayakumar@e4e.com

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Accenture hiring Medical Writer "A"

H and LS Medical Writer

1 - 3 Years

Chennai

Job Description

OVERALL PURPOSE OF JOB
Writing, Reconciling, editing and/ or managing the production of high quality clinical documents that are components of regulatory marketing approval. Knowledge of clinical terminology is a must. They ensure that documents are written consistent with company and regulatory guidelines.
PROCESSES :
.
Responsibilities/ Authorities :
oWriting first draft of Aggregate Report (e.g. RMP, PVP, PSURs, PADERs, ASRs, QSUSARs)
oLiterature Search
oNewly analyzed, ongoing and completed study information from, but not limited to, clinical, non-clinical, and epidemiology studies.
oCurrent Reference Safety Information (e.g., CCSI/ CCDS/ CPLP)
oConduct analysis of singles cases extracted
oEnsure consistency with quality, accuracy, and medical safety standards
oReview and follow-up reports with relevant stakeholders internally (Lead TA, local market PV, Global Regulatory Teams, Medical Surveillance Team, Pharmaco-epidemiology, etc.)
-Attaches/ reviews all letters and queries for appropriateness and completeness.
-Oversees all the team resources in the work.
-Oversee execution of Quality Control and discrepancy management for outputs
-Assist in training for new resources and as a part of continuous improvement
-Assist in the development of documentation such as work instructions or task checklists for readiness activities as required
-Ensure compliance with client and company policies
-Own assist and comply to all SLAs (Cycle time and quality)
Requirements:
- No special physical demands.
- Major part of work done in office environment.
- High degree of accuracy and attention to detail.
- Good decision making ability.
- Demonstrated strong writing skills and has written publications.
- Ability to analyze, understand and interpret complex scientific data from a broad range of scientific disciplines
    

Company Profile

Accenture

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