www.sr-te.com Sri Research For Tissue Engineering Pvt Ltd Bangalore : Clinical Trials Research Associate

[mskavi]

SRTE is a first generation technology led enterprise working which aims to translate cutting edge research of human tissue engineering to address several unmet medical needs. SRTE is looking for bright young people in various aspects of cell biology, clinical trials, general surgery to assist it translate tissue engineering science into a reality. You will have the opportunity to work with cutting edge science and realize the application of new technologies to those needy patients and also stay updated with new developments in science and technology.

Currently there are several open positions

Research Associate: Clinical Trials :
A M.Sc in biology/biotechnology or B.Pharma from a reputed University with about 2 years experience in handling clinical trial data. The job would involve the co-ordination with the clinical trial agency in acquiring trial data, carrying out the required analysis in support of on-going projects and presentation to regulatory authorities.

Senior Scientist: Cell Biology :
A Ph.D with about 2 -3 years of post-doctoral experience in area of cell biology with interest in human tissue engineering and medical applications of tissue engineering. The candidate would be responsible for developing and standardizing human tissue culture protocols for production scale tissue regeneration and clinical trials. He or she should be able to work in a group and preferably lead the scientific work at SRTE in the area of Tissue Engineering. The person will work closely with the management and the scientific advisory board of SRTE.

Research Associate: Human Tissue Culture :
A M.Sc in biology/biotechnology from a reputed University with about 2 years experience in handling human cell lines and cell/tissue culture processes. The position will report to Senior Scientist. The job would involve maintenance of human cell lines, carrying out as directed, tissue culture processes for various projects within the Company. Industry experience will be an added advantage but not a pre-qualification.prerequisite

Facilities and Laboratory Manager :
A M.Sc/ B.E(biotechnology) with about 5 years of experience in working in CGMP, Class 10,000 clean room facility for human tissue culture and must be well versed with the handling and maintenance of clean room facilities. The candidate will be responsible for the smooth running of the laboratory facilities and will be responsible for all the maintenance of the entire laboratory.

http://www.sr-te.com/careers.html

Contact us :
Sri Research For Tissue Engineering Private Limited
c/o Sri Shankara Research Centre
Rangadore Memorial Hospital
1st Cross Road, Shankarapuram
Bangalore - 560 004, Karnataka, INDIA

[Guest]

dear sir /mam
i have an expirience about 9 month as clinical research coordinator .can i apply for that .?


regards
kamal malhotra
apollo hospitals.
mobile-9971037600

[Guest]

T.T.D BHANU DEVAKANTH
Email : bhanudevkanth AT gmail.com

Objective :
To be professionally associated with an esteemed organization which progresses and given an opportunity to update my knowledge and enhance my skills in the state of latest technologies and work hard towards achieving the goals of the organization
EXPERIENCE SUMMARY
- 7+Years of diverse experience in Medical Marketing (4+ years) & Clinical Research (4+ years)
- 6months monitoring Experience in VIMTA Labs Ltd.
- 3months Co- monitoring Experience in zoom clinical trials Pvt ltd.
- 9months Monitoring Experience (Quality check) in Pinnacle clinical Research pvt ltd.
- Well acquainted to develop a comprehensive understanding of the protocol, protocol related schedule of events and procedures for overall compliance.
- Flexible and versatile to adapt to any new environment and work on any Clinical Trial.
PREVIOUS WORK EXPERIENCE
- Worked as a Medical Representative in USV ltd in Visakhapatnam, 2002 Oct to June2005.
- Worked as a Medical Representative in Group Pharmaceutical Limited, Aug 2005 to Jan 2007
- Worked as a Study Co-coordinator in Dept of Endocrinology, King George Hospital, and Visakhapatnam from May 2007 to Sep’2008.
- Worked as a study Co-coordinator in Zoom Clinical Trials, Hyderabad. from Sep’2008 To Oct’ 2009.
- Worked as a Sr.Coordinator in Site Management Organization ” Pinnacle Clinical Research Pvt. Ltd”, Hyderabad from Nov’ 2009 to Nov’2010 based at Vijayawada
CURRENT WORK EXPERIENCE
Working as a Clinical Research Associate in Clinical Research & Pharmacovigilance Division, VIMTA Labs Ltd, Hyderabad since Dec’ 20010 to till date.

Educational Qualification :
- Bachelor of Pharmacy, Aug 2001 from Shadan college of pharmacy, affiliated to the J.N.TUNIVERSITY OF HYDRABAD with 68.83%
- Professional Diploma in Clinical Research (PDCR), Sep 2007 from Catalyst Clinical services, New Delhi.
Knowledge Skills :
- Familiar with ICH-GCP, Schedule “Y”, ICMR,
- E-CRF Data Entry(Inspire),Inform
Technical Skills :
- Knowledge in MS office, Internet Browsing
- Trained in accessing the IWRS/IVRS
ICH-GCP TRAINING
- On site GCP training at Andhra Medical college, K.G.H on 2nd July by Novo Nordisk India Pvt ltd.
- Attended Investigator’s Meeting held on Aug 21-23, 2007 at Dubai.
- Attended Investigator’s Meeting held on May 29-30, 2008 at Cape Town by Novo Nordisk India Pvt ltd.
- Atteneded Investigator’s Meeting held on 17th/Feb/2010 at Goa by Parexel synchronous Pvt.Ltd, India.
STRENTHS :
- My communication skills have always been an asset during my Marketing work experience.
- Self motive starter and quick learner.
- Intense attention to detail the task.
- Hard working, sincere, innovative, adaptability in respective challenges.
- My positive and friendly attitude was always been a power house of energy to achieve anything.
Summary of Clinical Experience :
S.No Indication Clinical Trial Phase type Role Duration
1 Type-2Diabetes Phase-3 Study coordinator Feb’07-Apr08
2 Type-2Diabetes Phase-3 Study coordinator jun’07- Aug’08
3 Major Depressive Disorder Phase-2 Study coordinator Sep’08-Nov’09
4 Gastro-esophageal cancer Phase 3 Sr.Coordinator Nov’09-to
Mar’10
5 Type-2 diabetes Phase 3 Sr.Coordinator Feb’09 To Nov’10
6. Acid Peptic disorders PMS study CRA Dec’10 To till date
7 Acne Phase-3 CRA Dec’10 To till date
Primary responsabilités
- Primary person responsible for management of assigned sites, including acting as central point of communication between Company and Investigator sites
- Perform monitoring visits according to monitoring plan (including trial initiation, training and closeout)
- Participate in site nomination process, perform evaluation of site capability and make recommendation for inclusion in clinical trial
- Facilitate preparation, collection and distribution of trial master file documents
- Author study monitoring visit reports
- Set up and ensure maintenance of site master file
- Manage site IP supply and sample management during course of study
- Point of contact for sites and facilitator of communication between sites and key Company line functions
- Assure continual compliance with GCP, ICH and Company SOPs in informed consent process, source data verification, AE and SAE reporting, protocol execution, IP accountability, and other clinical tasks as specified
- Resolve deviations to standard by remedial action and training
- Escalate any issues regarding study conduct to Project Managers as needed
- Support the Project Manager as required in relationship management tasks (e.g. contracts, sample management, supplies, etc) and evaluating site performance
Secondary responsabilités - Collecting information for the potential investigator database
- Accompanying and / or helping Senior Management in coordinating activities in their region

[bhanudevkanth]

i am B.Pharm graduate with 4 yrs of experience, presently working as CRA in VIMTA Labs ltd,HYd since 7 months.

[Guest]

CURRICULUM VITAE
Patan Fayaz,
E-mail : fayaz.cology AT gmail.com .
Objective :
To be associated with an organization that would provide a challenging work atmosphere and an opportunity to learn, grow and contribute to its growth to the best of my Academic knowledge, skills and interest.
Academic Qualification :
Degree / Qualification Year of passing Grade (Percentage)
Master in Pharmacy (Pharmacology)
[Rajiv Gandhi University of Health Sciences, Karnataka, Bangalore.] 2009-2011 Ist yr 77.02%,
IInd yr Appeared. Thesis submitted (waiting for result.)
Bachelor of Pharmacy (B.Pharm)
[Acharya Nagarjuna University, Guntur, A.P.] April 2009 71%
Intermediate (PUC)
[Board of Intermediate Education, A.P.] March 2005 91%
SSC (10th)
[Board of Secondary Education, A.P.]
March 2003 75%
Academic Skills :
Subject recruitment and discussion of study procedures with subject and assisting in obtaining informed consent.
Having Knowledge on Ethical Guideline for Biomedical Research Involving Human Subjects.
Have good knowledge in Clinical trials.
Have basic knowledge on GCP in clinical Research.
Good interpretation skills.
Very Good in Animal handling (Rodents).
Familiar with statistical tools used in data analysis.
Well known in drug administration through various routes.
Strengths :
Good communication skills with Positive attitude.
Passion for learning new developments in the industry.
Excellent Team Work with supportive nature and dynamism.
Highly committed, Innovative, Self-Motivated and confident.
Professional Registrations :
Registered Pharmacist at Kanataka State Pharmacy Council.
Academic Experience :
- Attended the National seminar on “Role of Pharmacy Education in Scientific, Regulatory and Social Frontiers’ held at Hindu College of Pharmacy, Guntur.
- Attended the National seminar on “Emerging Trends in Clinical Research” held at Garden City College, Bangalore.
- Attended the seminar on ‘Advanced Biosciences’ held at Dayananda Sagar College of Arts, Science & Commerce, Bangalore.
Computer knowledge :
- MS-OFFICE
- Internet skills
- Computer Basics
Current project work in M.Pharm(Pharmacology) :

Title : Pharmacological screening of aqueous extract of Cyperus rotundus for anti
Obesity and Cardiovascular properties.
Guide ;: Prof. Rajeev Hiremath.

[Guest]

Curriculum Vitae
SIRIPURAM AMAR,
Email ID : amar.siripuram AT gmail.com

OBJECTIVE
To work in an innovative and challenging environment equipped with the state-of-art technologies that enhance my skill and knowledge that in turn contributes to the growth of the organization.
ACADEMIC PROFILE
- B.Pharmacy from Rajiv Gandhi University of Health Sciences, Karnataka with 65.75%, At D.R.Karigowda College of Pharmacy, Hassan. In the year of 2011.
- 10+2 (Biology, Physics Chemistry) from board of Intermediate, Andhra Pradesh with 78%, At Trinity Junior College, Karimnagar .In the year of 2006.
- SSC from Board of Secondary Education with 78.5%, At Sarvodhaya High School, Karimnagar. In the year of 2004.
TECHNICAL SKILS

Quality control of tablets,capsuls and parentrals.
Capable of operating dissolution apparatus, disintegration apparatus.
SOFT SKILS
MS-office,
STRENTHS
- Positive attitude & confidence.
- Fast learning.
- Self-motivated and Hard worker.
- Innovative thinking
ACHIEVEMENTS
- I got school first throughout my higher education.
- I have participated in technical quiz in college and I got second prize.
- Participated in technical events and cultural events conducted in college.

FILED OF INTEREST
- Production department.
- Qualitycontrol department.
- Quality assurance.
- Research & Development.
- Regulatory affairs..

Declaration :
I here by declare that the above details are true to the best of my knowledge and I am personally responsible for the authenticity of the same.
Place : siripuram amar
Date :

[Guest]

Sir /Madam,
With respect to the above mentioned subject, I offer myself as B.Pharm candidate working as Research Associate in Clinical Unit in Axis Clinicals Ltd, and wish to give my candidature for post in our esteemed organization.
I am herewith enclosing my candidature and provide my opportunity to serve your reputed concern, for which I assure you the best of my service.
Thanking you,
Yours sincerely,
E.Rajesh Kumar
CURRICULUM VITAE
E.Rajesh Kumar
E-mail : rajee_642 AT yahoo.com
Research Associate
Summary
- Synopsis
A creative and enthusiastic professional with excellent communication, presentation and negotiation skills, which I have developed through my education and work experience, in planning and in executing tasks as appropriate to the timely accomplishment of objectives.
Professional Experience
- Work Experience
- Presently working as Research Associate in clinical unit from june 2009
- 2 years 10 months of work experience as Clinical Research Associate . Joined as Research Associate-I and presently working as Research Associate-III in Clinical Pharmacology Department, Axis Clinicals Limited (formerly Trident Life Sciences Ltd.), Hyderabad, India, which is approved by DCGI, NABL, ANVISA Brazil and has a standard of ISO 2000-2001 and has ANDA approvals from different regulatory regions like US FDA, WHO, Health Canada, UK MHRA and ANVISA Brazil.
- Audit Experience
- Active participation in external auditing from different Regulatory Environments like FDA - US (Twice), MHRA-UK, ANVISA – BRAZIL (Twice), AFSSAPS – France, DCGI, ISO (Twice) and Pollution Control Board.
- Experienced in different Audits from several sponsor companies located in several regions of the world like US, Europe, South Africa, Korea and India.
- Have a thorough understanding of ICH-GCP.
Work Summary
- Clinical Research Associate Experience
- Conducting study’s on healthy volunteers and monitors the safety and adverse events of the subjects.
- Updating the IRB with adverse event related issues.
- Clinical Report preparation and Analysis of adverse events
- Preparing AE reports, updating the Sponsor with the adverse events and handling Post Study follow up of subjects. Handling subject compensation related issues.
- Review of protocol and related documents like informed consent documents, clinical review reports, drug shipping documents etc.
- Monitoring all the study related activities and has volunteer interaction.
- Preparing the CRF’s and Trial Master Files.
- To obtain inform consent form from study subjects
- Archiving of the study related documents for regulatory follow-up.
- Quality Control Personnel Experience
- Reviewing of Protocols, Informed Consent Forms, Investigators Brochures, Study Information to volunteer and Case Report Forms.
- Checking the project initiation, maintenance & close-out documents.
- Checking all the IRB/IEC related correspondence.
- Checking the Clinical Study Reports and Tables.
- Reading, understanding, and analyzing AE reports, updating the Sponsor with the adverse events including checking for completeness of the adverse events and safety narratives.
- Updating the sponsor with all the aspects of study.
- Ensuring smooth conduct of the clinical phase of the study. Responding to QA audit findings and Sponsor audit findings by both in process and retrospective analysis. Resolving queries in the study related data like CRF and Clinical Reports before submission to Regulatory authority.
- Preparing and reviewing of SOP's, Working Instructions, Flow charts and Emergency action plans as per ICH-GCP for Clinical Unit.
- Monitoring all the study related activities.
- Inter-Relations
- Auditors, IRB/IEC, Sponsors, Visitors etc.
- Principal Investigator, Clinical Investigator, Quality Assurance Department, Volunteer Mobilization Department, Instrumentation Department, Business Development Team and all other study personnel as per the study requirement.
Pharmacist Experience
- Worked as a pharmacist in axis clinical limited it involves study drug receipt, physical verification of drugs, blinding,unblinding,allocation code, drug description, Dispensing, Accountability and archival of drugs for various studies.
- Have well experience in pharmacy audits of various Regulatorys (Drug Accountability) like US FDA, UK MHRA, and BRAZIL ANVISA etc.
Areas of Interest
Pharmacovigilence, Medical Writing, Clinical Trials Phase I-IV, and Regulatory Affairs,
Educational Qualifications
- B. Pharmacy : B. Pharmacy from St.Peters institute of pharmaceutical sciences from kakatiya University,
- Certification Programs
- Attended workshop on "GCP and Clinical Research" conducted by Clinical Pharmacology Department at Trident Life Sciences Ltd., Hyderabad.
- Participated in "Bio-Medical Waste Management, Handling and Safe Disposal Options" conducted by Semb Ramky Environmental Management Private Limited., in Trident Life Sciences Limited, Hyderabad.
- Participated in KRA (Key Role Areas) workshop organized by Price Water Coopers in Axis Clinicals Ltd.

- Seminars
- ICH-GCP Basic Concepts by Dr. K. Sanjeeva Reddy.
- Auditing of Clinical Research Studies by Dr. A. Jaya Chandra Reddy.
- Pharmacovigilance by Dr. Anitha Singa Reddy.
Software Skills
- Computer Knowledge
- Operating System : WINDOWS 98/2007
- Packages : MS Office 2003
Declaration
I hereby declare that all the information furnished above is true and correct to the best of my knowledge and belief.
(E.Rajesh Kumar)

[Guest]

RESUME
Hamed Ali. Shaik
:Email:pharma_hamed51 AT yahoo.com
OBJECTIVE :
Seeking a challenging position in an esteemed organization where the skills and abilities I possess in the field of pharmacy can be put to best of its use and to fulfill both organizational as well as personal objectives.Further wish to see myself established and grow in great organization.
ACADEMIC PROFILE :
- Post Graduation M.pharmacy (pharmacology) from Anurag Pharmacy college , Jawaharlal Nehru Technological University , Hyderabad with an aggregate of 75%
- Graduation B.pharmacy from Blue Birds College Of Pharmacy ,Kakatiya University ,Warangal with an aggregate of 65%
- Intermediate (B.p.c) from Sri Chaitanya junior College, Hyderabad with an aggregate of 81.1%
- SSC from Vikas High School, Guntoor with an aggregate of 85%..
COMPUTER SKILLS :
Profound knowledge in operating programmes like MS OFFICE and ‘C’.
SEMINARS AND WORKSHOPS ATTENDED ::
- Presented a poster on “Therapeutic Drug Monitoring” in a National level pharmacy meeting conducted by All India Council for Technical Education at Jayamukhi College of Pharmacy in Narsampet in the year 2009.
- Presented a poster on TAY-SACHS disease in one day workshop conducted by EVER GREEN LIFE SCIENCES
- Attended as a delegate for the 62nd Indian Pharmaceutical Congress , Manipal
- Presented a poster on “preparation and Evaluation of Aceclofenac Niosomal Gel” at 62nd Indian Pharmaceutical Congress, Manipal.
- Presented a poster on “Bridging Gap between Academia and Pharmaceutical Industry” in Anurag pharma Quest-2k11 held at Anurag College of Pharmacy, Kodad.
- Attended an International Conference on “Imbibing Pharmaceutical Knowledge to the Professionals” Held at Lalitha College Of Pharmacy, Hyderabad.
- Attended Workshop and Seminar on “Readdressing thoughts on animal care and handling as per CPCSEA guidelines” Held at Lalitha College of Pharmacy, Hyderabad.
- Got First place in Debate competition in “Inter Pharmacy College Competition” held at Anurag College Of Pharmacy , Kodad.
- Presented a poster on “Conventional Therapy on Leprosy” at 63nd Indian Pharmaceutical Congress, Banglore.
PROJECT WORK :
Study of Anti Diabetic activity of Terminalia pallida on Streptozotocin induced diabetic rats.
PUBLICATIONS :
- Published a Research article on In-vivo screening of Bougainvillea glabra leaves for its Analgesic, Antipyretic and Anti-inflammatory activities in Asian J. Res. Pharm. Sci. 2012; Vol. 2 : Issue 3, Pg 85-87.
- Published a review article on pharmacognostics and pharmacological profiles of nardastachys jatamansi dc in Elixir Pharmacy online journal 39 (2011) 5017-5020.
TESTS TAKEN : GRE and TOEFL
AREAS OF INTEREST :
- Pharmacovigilence
- Clinical research.
- Drug safety
Declaration :
I hereby declare that the information given is true to the best of my knowledge.
Place : Zaheerabad Date: . (HAMED ALI SHAIK)