Parivar Seva Sanstha Chennai : Lady Doctor, Medical Officer

[mskavi]

Parivar Seva Sanstha
http://www.parivarseva.org

Keywords: Medical Officer, Female, Parivar Seva Sanstha, Chennai

Company Profile
Parivar Seva is a national NGO providing reproductive health services with emphasis on family planning. Registered in 1978,the organization today has a strong network of 35 reproductive health clinics, contraceptive products marketing and distribution system and numerous projects and outreach activities located in 21 states of India. Through its various programmes the organization cares for more than1500, 000 women and men every year .A number of interventions of the organization are strategically executed in states declared backward. On the basis of socio- economic and health parameters by the Government of India, Including Rajasthan, UttarPradesh, Madhya Pradesh Bihar, Chattisgarh and Orissa.
The thrust areas of work of Parivar Seva are Social Marketing of Clinical Services,
Social Marketing of Contraceptives, Reproductive Health Education and Training/
Family Life Education.
Clinical Services:
Parivar Seva /Marie Stopes Clinic
Parivar Seva has a holistic approach towards improving the quality of life of men and women through accessible, affordable quality reproductive health and family planning services, contraceptive products and information and education activities. The 44 female clinics and 1 male clinic spread across number of districts of 12 states meets the demand of RH and FP services through a team of highly skilled medical doctors, counselors, lab technicians, community workers and promoters.
SRHET (Sexual & Reproductive Health - Education and Training):
Division is working towards creating awareness, educating and training adolescents, youth, about to be married youth and married couples in reproductive age groups, in the field of reproductive & sexual health. The objective is to help people lead a healthy reproductive life and plan their families.
Social Marketing of Contraceptive Products:
Under the umbrella of GOI?s social marketing programme for contraceptives. Parivar Seva markets its own brand of contraceptives at subsidized rates. The CSMP ensures easy accessibility to the temporary contraceptive methods to people in towns, villages, remote and inaccessible areas. The CSMP division has a strong and effective distribution network with motivated and dedicated staff.

Lady Doctor (Chennai)

Experience:
0 - 5 Years
Location:
Chennai
Compensation:
Rupees 1,75,000 - 2,50,000
Salary is not a constraint for deserving candidate.
Education:
UG - MBBS - Medicine

PG - M.S/M.D - Gyneocology, Obstretrics
Industry Type:
Medical/ Healthcare/Hospital
Functional Area:
Healthcare, Medical, R&D
Posted Date:
12 Sep


Job Description
--To perform MTP upto 20 weeks including pre & post procedure care.
--Deliver all family planning services, including sterilization services (Laparo/minilap)
--Provide other Gynae services including infertility
--Responsible to ensure quality of care particularly infection prevention practices
--Maintenance of records & Reports
--Procurement and judicious utilization of Drugs & other consumable.
--Able to handle basics emergency in the clinic
--Update & maintain the knowledge & skill of Para-medical staffs in the team

Desired Candidate Profile
Essentail: MBBS, DGO, M.D. M.S Desireable:
House job in Obs. & Gynae or 1 year experience in Obs. & Gynae from a recognized Hospital

Contact Details
Executive Name:
Mayank Kapoor

Address:
Parivar Seva Sanstha
C-374, Defence Colony
New Delhi,DELHI,INDIA 110024

Email Address:
hr_pss@airtelmail.in

Telephone:
91-11-24337712

Reference ID:
Lady Doctor/Chennai/003

[Guest-IJT]

Hi,


I have 2.5 yr work experience in Nair Hospital, Mumbai (for WHO & DCGI project of ADR monitoring )and Reliance clinical research services, Mumbai India in Pharmacovigilance department.

Please view my CV/Resume for consideration for any vacancy in Pharmacovigilance team.

Best Regards

Neelam Mahaparale

SUMMARY

I have 2.5 years of experience in Clinical research with skills in Clinical operations, Pharmacovigilance & Data management which gave me excellent knowledge of GCP and ICH guidelines, Microsoft Windows, Microsoft office.

My work for ‘Adverse Drug Reaction (ADR)’ Monitoring Program governed by WHO and Drug Controller General of India (DCGI), helped me gaining exceptional knowledge in Pharmacovigilance domain.

As I have worked for hospital as well for CRO has good knowledge of working procedures for both Principal Investigator and Sponsor. My knowledge is excellent not only in clinical but also in Preclinical studies and patent law.

To enlist some of work responsibilities:
Pharmacovigilance:
--Medical monitoring plan writing
--Operational support in AE management to Clinical Operations group
--SAE collection, evaluation, classification and reporting
--Medical Monitoring Plan writing
--SAE reconciliation

Clinical operations:
--Feasibility survey
--Assistance in preparation of local study related documentation including Clinical Study Timelines, recruitment plans and Informed Consent Form
--Support for planning and execution of studies
--Coordinate supply of clinical study equipment/ drugs
--Review adherence to SOP and GCP
--Submission and archival of study documents

Data Management:
- Preparation of study related documentation & Timeline,
- To ensure Statistical Analysis Plan (SAP) requirements
- SAE Reconciliation
- Coding of adverse events (MedDRA)
- Medical Coding - Coding of concomitant drugs (WHODRUG)
- Data Validation and Query Management
- Periodic validation of CRF data

PROFESSIONAL EXPERIENCE

1) Reliance Clinical Research Services Pvt. Ltd.
(December 2004- April 2006)

Designation: Executive Medical affairs
(Pharmacovigilance Associate & Clinical Data Coordinator)

Clinical Research Experience:

Indication of study / Disease Role(s) in study
Oncology Safety Officer / Pharmacovigilance Associate
(SAE collection, evaluation, classification, and reporting)
Clinical data coder
(Coding clinical data SAE reconciliation)
Oncology Safety Officer / Pharmacovigilance Associate
(SAE collection, evaluation, classification, and reporting)
Oncology Safety Officer/ Pharmacovigilance Associate
(SAE collection, evaluation, classification, and reporting)
Probiotic formulation in Nephrology Safety Officer/ Pharmacovigilance Associate
(Medical Monitoring Plan writing, SAE collection, evaluation, classification, and reporting)
OTC product in Osteoarthritis Pharmacovigilance Associate
(MMP Writing, SAE collection, evaluation, classification, and reporting))
Ophthalmology Pharmacovigilance Associate
(SAE collection, evaluation, classification, and reporting)
Vaccines Pharmacovigilance Associate
(Medical Monitoring Plan writing)
Cardiology Pharmacovigilance Associate
(Medical Monitoring Plan writing)
Infectious Diseases Pharmacovigilance Associate
(Medical Monitoring Plan writing)
Respiratory Feasibility
Wound healing Clinical Data Coding and SAE Reconciliation
Ophthalmology Clinical Data Coding and SAE Reconciliation

2) Clinical Pharmacology Department, Nair Hospital, Mumbai.
(From January2004 to December2004)
Designation: Research Associate.

- ‘Adverse Drug Reaction (ADR)’ Monitoring Program governed by WHO and Drug Controller General of India
- Drug Information Services.
- Assistance in a Clinical Trial.
- Therapeutic Drug Monitoring
- Anti-Epileptic Drugs
- Immunosuppressant (Cyclosporine)
- PEG estimation in Urine using Spectrophotometer.

Clinical Research Experience:

Indication of study / Disease Study type and phase Role(s) in study
Diabetes Mellitus Phase I, ICMR sponsored Study Coordinator
Alcoholic Cirrhosis Phase III, CDRI Sponsored Study Coordinator

Workshop Attended:

- 2 Days state level work shop on Intellectual property rights – a pharmaceutical perspective 23th& 24th Feb. 2010
- Pharmacovigilance- a solution to drug safety, 13th Feb. 2010
- Pharma Pulse confluence Advanced Clinical research & GCP Workshop, 26th& 27th Feb. 2005
- Pharma Pulse confluence Pre-Clinical research, 24th& 25th Feb. 2005
- ICMR Workshop on Clinical Research Methodology, 2004.

Personal information
Nationality Indian

Education
Course Year of Passing Subject / Specialization Institution / University
B. PHARMACY 2002 Pharmaceutical Sciences Bharati Vidyapeeth’s College of Pharmacy/ Mumbai
PGDCRP
(Post Graduate Diploma in Clinico-Regulatory and Patents) 2005 Clinical Operations, Regulatory Affairs, Patent Law. R. N. Ruia College-PEXA (Pharmaceutical Experts Association) / Mumbai.

Languages Known

- English Business to Native level
- Japanese Basic level
- Hindi Native level
- Marathi Native level

References

- Dr. Urmila Thatte (Clinical Pharmacology Dept. K.E.M.Hospital Parel, Mumbai)
- Dr. Mahajan (Cardiology Dept, Sion Hospital, Mumbai)