www.anantco.com Anant Co Enterprises Pvt Ltd Delhi : Resident marketing manager

[mskavi]

Anant Co Enterprises Pvt Ltd
http://www.anantco.com

Anant Co Enterprise : Delhi : Resident marketing manager
Keywords: sales and customer liasion

Company Profile
Established business group in diversified fields for more than 50 years with pharma as core business.Represent worldwide manufacturers,exporters for their sales in India.

Resident marketing manager

Experience:
3 - 5 Years
Location:
Delhi
Compensation:
Rupees 4,00,000 - 6,00,000
Education:
UG - Any Graduate - Any Specialization

PG - M.Sc - Chemistry
Industry Type:
Pharma/ Biotech/Clinical Research
Functional Area:
Marketing, Advertising, MR, PR
Posted Date:
03 Sep


Job Description
marketing/import indenting bulk drugs,API,pharma intermediates/liasion with customers in north india territory for our foreign principals.

Desired Candidate Profile
experience in import indenting of bulk drugs/api/intermediates,north india pharma customers contacts.

Contact Details
Executive Name:
Mr. Ramesh Mahajan

Address:
Anant Co Enterprises Pvt Ltd
194, Arvind Chamber
Gauri Studio Compound
Western Express Highway
Mumbai,Maharashtra,INDIA 00

Email Address:
mahajan@anantco.com

Telephone:
91-022-67685000

[Guest-IJT]

Dear Sir,
Kindly find the updated resume for Pharmacovigilance/Drug Safety position in your esteemed organisation.

Thank you.

Dr Srinivas Vasam
[EMAIL="drvasam@rediffmail.com"]drvasam@rediffmail.com

CURRICULAM VITAE
Dr Srinivas N Vasam
Mumbai - 400018.

Contact Details:
Mobile: +91 99 6705 2780
Email ID: [EMAIL="drvasam@rediffmail.com"]drvasam@rediffmail.com

Objective:
o To gain experience in pharmaceutical industries/BPO/ Healthcare industry by doing research / Medical Coding, where I can develop personal and professional skills.
o To obtain a responsible and challenging position where my education and work experience will have valuable application.

I. Current Designation:
Sciformix Technologies Pvt Ltd.
As Safety Data Analyst
Since Feb 2010

Perform initial checks in source documents and initial follow-up for the case.
Ensure scientific rigor through accurate, complete and consistent data entry (coding MedDRA) of adverse event reports from source documents with emphasis on timeliness and quality.
Labeling
Case narrative writing,
Evaluate and processing of expeditable and non-expeditable AE reports.
Identification of clinically relevant information missing from case report by preparing follow-up request as needed to HCP or Patient.
Soft and hard copy documentation: As per client requirement with naming conventions
All source documents.
All follow-up documents, i.e Fax, email and call.
All case file notes and Batch verifications
Email communication and Acknowledgments
Quality cases.

2. Tata Consultancy Services, Life Sciences and Health Care. Mumbai
One of Big Pharmaceutical Company in Europe, Project in Pharmacovigilance,
As Drug Safety Associate (Senior Process Associate),
Since July 08 to Jan 2010.

Certified from ICH GCP guidelines.
Activity:
SAE receipt, case initiation, case inactivation, labeling, data entry (Medical coding), scientific assessment, medical review and Letter/ report (narrative) writing and sending and closing the report on database.
Job Description:
Reports received from global sources.
Reports are both spontaneous and clinical.
Reports come from three different groups.
Send queries on discrepancies to sender.
Many types of information to be entered.
Send queries on discrepancies to sender.
Timelines are tight to ensure as much time is possible for scientific and medical assessment.
Interact with sender of report for clarifications.
Interact with Roche Central Operations to confirm invalidity of report/case.
Vital that only truly invalid cases are inactivated.
Requires medical judgment and knowledge of adverse events and drugs.
Labeling documents can be complex.
Highest complexity role.
Requires detailed medical knowledge and products.
Interacts with Drug Safety Associate who performed scientific assessment.
Must incorporate comments and changes from medical review
Send letters and reports globally.

II. Neeman Medical International, Clinical Research Services (CRO), Mumbai.

As a Clinical research coordinator mainly in Oncology trials.
Since May 2007 to July 2008.
Certified for GCP guidelines and monitoring from Neemanasia Medical International.

Activity:Clinical Research Professional (Clinical research Coordinator) Varied Experience in Clinical Research Project Coordination and Management, Data Analysis and Report Writing in mainly oncology trials.

Clinical Experience:
o Monitoring the patient on Chemotherapy for the side effects.
o Monitoring P K sampling collection during trial.
o Execute and Manage study startup, conduct and close out.
o Counseling patients & their Relatives regarding their disease and trial.
o Interact with Sponsor & monitor during site survey, monitoring visit.
o Ensure clinical trials meet highest standards of ICH GCP and SOPs, as well as compliance to global/local guidelines in terms of medical, ethical and regulatory requirements.
o Attended 4 monitoring visit for the Phase-III trial in Oncology.
o Attended 3 Site qualification visit for Phase-III trial in Gynecology.
o Attended 2 internal QC visit in Neeman for different protocols.
o Attended 6 co - monitoring visit for the Phase-III trial in Oncology.

Job Roles & key Accountability.
Maintain and update source documents and site files for external and internal audits.
Maintain quality and timelines of assigned project work.
Performance, Integrity and Commitment
Review and discuss Protocol, Case report form and Inform Consent forms.
To Remain adhere with ICH-GCP, SOPs, Hospital Policies and Regulatory.
Problem Solving: Resolving DCF during Study.

Job Profile:
To obtain IRB approval for protocol, advertisements, and informed
To read and understand the information provided on the test article.
To ensure all personnel involved in the study are informed of their study obligations.
To obtain proper written informed consent from each study subject prior to Participation in the study.
To adhere to the sponsor/CRO’s protocol.
To Perform study initiation & to be responsible for the conduct of the study.

o To notify the IRB of study changes, provide at least annual progress reports, and prepare a final study report.
To report serious adverse events promptly to the IRB and Sponsor/CRO
To maintain adequate and accurate case histories for each study subject that records all observations and data during the study.
To maintain accurate and complete records of the receipt, administration, and return of all clinical supplies. All discrepancies are noted and explained and ordering laboratory kits accordingly.
To permit Sponsor/CRO's representatives to inspect records of the study.
To prepare and assist Site Initiation Visits, Interim Monitoring Visits.

III. Nair Hospital, Mumbai.
Sponsor: Cipla ltd
As a Clinical research coordinator in Chest Medicine.
Since December 2006 to April 2007.
Certified for ICH GCP guidelines and monitoring from Cipla Ltd.

Job Description:
Responsible for conduct of trials with compliance to GCP/GLP requirements
Facilities monitoring and auditing by the sponsor and inspection by the appropriate regulatory authorities
Responsible to ensure proper communication with sponsor/ ethical committee
Responsible to ensure communication of adverse event to sponsor/ ethical committee
Responsible to ensure accountability of study drugs
General screening of clinical trial
Obtaining informed consent of volunteers.
Professional Experience as a Resident Doctor:

Hospitals Location Time Period
Ramlayam Hospital Nashik Feb 2005-Sep 2005
Irla Nursing Home Vile-Parle Nov 2005-Apr 2006
Shah Nursing Home Matunga May 2006-Nov 2006

Educational Qualifications:
Degree University Year
SSC Maharashtra State Board 1997
HSC Maharashtra State Board 1999
BHMS Nasik University (MUHS) 2005
PG Diploma in Clinical Research & Data Management. ACIMS Mumbai 2007
PG Diploma Psychology & Counseling
IBMS Chittor (A.P) 2008

Professional Courses:
Diploma in Clinical Research and Data Management from AICMS
Post Graduation Diploma in Psychology & counseling.

Computers knowledge:
o MS Office
o Power Point
o Internet browsing

ICH-GCP – Training attended in clinical research.
CIPLA PVT. LTD
NEEMAN MEDICAL INTERNATIONAL.
TATA CONSULTANCY SERVICES.

Key Competence:
People and Time management.
Excellent Analytical skills.
Ability to work under pressure.
Effective interpersonal skills
Planning + Team Work +Honesty = Quality Work.