www.zoomclinicaltrials.com ZOOM Clinical Trials Pvt Ltd Clinical Hyderabad : Research Coordinator

[mskavi]

ZOOM Clinical Trials Pvt. Ltd.

Clinical Research Coordinator
Overview :
Coordinate and participate in clinical research studies conducted by performing a variety of subject care and administrative duties to support activities that meet objectives of assigned research protocol(s).
Job Responsibilities :
Coordinate for site selection and study feasibility assessments.
Provide subject care and data collection procedures in adherence with the assigned study protocol and in accordance with good clinical research principals.
Ensure that IRB approval of protocol and informed consent form is obtained prior to initiation of the study.
Review subject charts, database records, and other sources to screen and identify potential subjects for inclusion in study based on criteria described in the protocol.
Confer with subject and physician to explain purpose of study. Coordinate to obtain written consent for subject to participate in a study prior to initiation of any protocol procedures.
Maintain accurate records of the receipt, inventory, and dispensation of study drug and materials.
Obtain and coordinate subject blood samples, cultures, tissues, and other specimens for laboratory analysis as described in study protocol
Collect pertinent information and data from subject charts and records, subject interviews, and other sources. Complete case report forms (CRFs) in accordance with research protocol guidelines.
Inspect CRFs, source documentation, and study files to ensure completeness.
Review CRFs, source documentation, and study files with representative from CRO/Sponsor at each visit. Make necessary corrections to CRFs and submit requested documentation in a timely manner.
Comply with standard operating procedures of the CRO/Sponsor, institutional review board (IRB) involved with the trial.
Compile and submit reports, documents, and correspondence as necessary to the IRB, CRO/Sponsor.
Provide training and direction to assistants or new personnel on protocol procedures.
Review journals, abstracts, and scientific literature to keep abreast of new developments.
Qualification/Experience
Bachelors or advanced degree (M.Sc, Pharmacy, Biotechnology) in life sciences or related field.
A minimum of 1 year experience working at a site.
Good knowledge of ICH-GCP
Effective communication skills (both verbal and written) are a must for this role.

Please forward Position number with your resume/CV for prompt and confidential consideration : careers@zoomclinicaltrials.com

Contact us :
Plot No : 8-2-684/4/16, Road No. 12
Anand Banjara Lane,
Banjara Hills,
Hyderabad- 500 034 AP, INDIA

Email : contact@zoomclinicaltrials.com

Web : http://www.zoomclinicaltrials.com

[Guest]

Respected sir,
i send my resume,very interested to work in CRO industry
CURRICULUM -VITAE
Dr. SRINIVASARAO BHIMALA( PT)
E-mail :drbhimala AT gmail.com

CAREER OBJECTIVE :
To seek a challenging career in an organization that could enable to bring the best out of me and thus leading to the firm’s development and growth of the organization.
EDUCATIONAL QUALIFICATION :
- BACHELOR OF PHYSIOTHERAPY (BPT) from Dr.NTR UNIVERSITY OF HEALTH SCIENCES,VIJAYAWADA.
- PRE CLINICAL TRIALS TRAINING ALONG WITH SAS APPLICATIONS FROM
MEDI INFORMATICS, VIJAYAWADA.
JOB PROFILE :
- Responsibilities include study of data by producing TLF s ( tables, listings and forms) as per 21 CFR USFDA guidelines.
- Main thrust areas include presentation of demographic data, AE/SAE analysis reports, comparison of efficacy of the investigational product with respect to market available drug in intermittent analysis.
- I have been extensively involved in clinical trial projects that comprises of statistical application in SAS environment to find out the efficacy and safety of the drug.
- Can handle clinical study reports regarding phase1- phase II trial.
- TECHNICAL SKILLS :
- Base SAS,
- MS DOS, WINDOWS OPERATING SYSTEMS.
EXPERIENCE :
- Worked as a CLINICAL TRIAL ASSOCIATE in MEDI INFORMATICS, VIJAYAWADA from January 09 to March2011
- Worked as a PHYSIOTHERAPIST in SMILE PHYSIOTHERAPY CLINIC, VIJAYAWADA from June 08 – September to January 09.

OTHER ACTIVITIES :
- Participated in workshops regarding micro oscillations for mobilization of spine.
- Participated in workshops regarding chest physiotherapy.
- Participated in ICH-GCP clinical research work shop conducted by cliniminds.
PROJECT DETAILS :
- BPT Project : PARKINSON’S DISEASE

[Guest]

CURRICULUM VITAE
ASRA ANWAR
e-mail : asra_anwar3 AT yahoo.com

OBJECTIVE :
Intend to build a career with a leading corporate with committed and dedicated people, which will help me to explore myself fully and realize my potential.
SOFTWARE EXPOSURE :
Language : C
Operating Systems : Windows 9x/xp
ACADEMIC DETAILS :
Course Institution Affiliation Year of Passing Percentage of Marks
High School International School (I.E.A) ICSE 2003 64
Intermediate
(BPC) Sri Chaitanya Jr. College BOI 2005 87
B.Tech
(Biotechnology) Malla Reddy Engineering College (MREC) JNTU 2005 - Present 64
SUMMARY OF EXPERIENCE :
- Dedicated Imaging Assistant with 1.4 year experience in Medical Imaging in Parexel International (India) Pvt.Ltd.
- Comprehensive experience in various indications including Site standardization, Site Management.
- Ensure the site personnel have a good understanding of the requirements of the study working with investigator sites on site surveys and site qualification.
- Involvement in site calls and site trainings.
- Monitoring within assigned projects of Good Clinical Practices (GCP).
- Mentor and assist in training internal personnel.
ACADEMIC ACHIEVEMENTS :
- Presented a paper on “cloning”, during the technical festival, in our college.
- Completed an industry oriented mini project at SHANTHA BIOTECHNICS Limited , Hyderabad on An overview of pertussis disease, prevention, vaccine manufacture during May-June ‘08
- Attended a 2-day conference on “NanoBioSaccharides Dissemination Conference” held during September 18-19,2008 at the University of Hyderabad, India
SKILL SET AND AREAS OF INTEREST :
Areas of Interest : Molecular Biology, Forensics, Microbiology, Genetic Engineering,
, Plant Biotechnology.
Lab Skills : Familiar with r-DNA technology, Quantitative assays of proteins &
DNA, Qualitative assays of Carbohydrates, few Immunological
Assays, determining growth parameters in case of bacteria at
Different substrate concentration, few biochemical assays, paper
Chromatography, TLC, Cell disruption techniques.
Extra-Curricular Activities :
- Active participation during school events.
- Have played badminton, kho-kho and table tennis during intra-school annual sports.
- Passion for dramas and theatres has encouraged me to stage few plays during school and college functions.

[sri.gowri77@gmail.com]

RESUME
T.J.SRI GOWRI
E-mail :sri.gowri77 AT yahoo.com
OBJECTIVE :
To pursue a challenging career in a clinical research industry and to become a part of esteemed organization that gives me scope to enhance my knowledge and skills.
EDUCATION :
COURSE NAME OF BOARD/UNIVERSITY YEAR OF PASSING PERCENTAGE
M.Sc in clinical research
management
ICRI,Hyderabad
2011
83%(up to 3rd semester)
Waiting for final semester results
B.Sc
(Biotechnology,Biochemistry, Chemistry)
Osmania University,
Hyderabad
2009
75%
Intermediate
Board Of Intermediate Education,A.P.
2005
90.5%
SSC
CBSE, Hyderabad.

2003
76%
ADDITIONAL QUALIFICATIONS :
- PG Diploma in Pharma Business Management.


PROJECTS :
- Institute of Clinical Research (India), PRIST university-A project
on “An observational study on prevention of Venous Thromboembolism in
patients undergoing Elective Total Hip Replacement Surgery”-2011,
in partial fulfillment of the degree of PG in Clinical Research Management.
- Institute of Clinical Research (India), Hyderabad- A project on “A study of
efficient working capital management for maximum profits at Natco Pharma
ltd”-2009, in partial fulfillment of the degree of PG diploma in Pharma
Business management.
- Institute of Clinical Research (India), Hyderabad- A project on “Case studies
review of efficient outsourcing management for maximum savings and
proficient services”-2010, in partial fulfillment of the degree of PG diploma in
Pharma business management.

TECHNICAL SKILLS :
- Knowledge of computer- M.S.OFFICE APPLICATIONS, INTERNET APPLICATION
- SAS
STRENGTHS :
- Good Knowledge on ICH GCP, Indian GCP, regulations in clinical research and regulations in Pharmacovigilance.
- In-Depth Knowledge about the Methods, Principles of Clinical Practices and clinical trial processes.
- Ability to grasp quickly, enthusiastic to learn new Professional aspects.
- Good communication and interpersonal skills.
- Ability to act as a team player.
- Keen observer.
WORK EXPERIENCE :
- Working as a Study Coordinator in Yashoda hospitals, Secunderabad, Andhra Pradesh since August 2010.
- Handled projects sponsored by Zydus Cadella,Cipla,AstraZeneca

[Guest]

Resume
K.Lavanya
E-Mail ID : kommareddylavanya AT gmail.com

CAREER OBJECTIVE :
To scale up heights in professional organization and take up a challenging career where I can exhibit my skills and strength in conjugation with my organization goal.
ACADEMIA :
2009 - 2011 M.Sc Microbiology from Osmania University with an aggregate of 71%
2005 - 2008 B.Sc Microbiology, Botany, Chemistry from St. Francis Degree College with an
aggregate of 67%
2003 - 2005 Intermediate from Board of intermediate with an aggregate of 67.5%
2002 -2003 SSC from Little flower high School with an aggregate of 75%
CERTIFICATION :
Jul 2011 to Aug 2011Undergone one month training in Clinical Trial Management and Regulatory affairs at Consortium Clinical Research Pvt. Ltd.
TRAINING :
- Underwent Training in Protocol Details, SAE reporting and Timelines for reporting, Pharmacovigilance, Schedule Y,ICD guidelines and Good Clinical Practice sessions at, Consortium Clinical Research Pvt. Ltd, in 2011.
CLINICAL RESEARCH EXPERIENCE :
Underwent on job training from 17 Aug 2011 to 17 Sep 2011 on :
- Maintaining current contact information for each assigned investigator site, as
well as preparing investigator site file for participation approval.
- Participate in the preparation of project and study related documents including
Informed Consent Forms (ICFs), synopses, protocols and amendments.
- Assist in the preparation of study protocols and ICD
COMPUTER SKILLS :
- MS office, MS word, MS excel and Power point presentation - Efficient in internet browsing and fast typing.
ACHEIVEMENTS :
- Won a prize in essay writing at school level.
- Participated in several cultural programs.
LEISURE ACTIVITIES: Solving SUDOKU, trekking and drawing