www.act-india.com Asian Clinical Trials Hyderabad : Clinical Research Associate

[muthukalee]

act-india.com
Clinical Research Associate

QUALIFICATIONS

Education : Graduate or post graduate degree in life sciences, nursing or other health related science For e.g. BSc, MSc, BPharm, MPharm and MBBS

Minimum Work Experience : 1 - 2 years of relevant work experience recommended

Preferred Skills :
Good written and verbal communication skills in English.
Computer literacy : MS Office
Attention to detail
An understanding of the ICH-GCP, CFR and local regulatory guidelines

Attributes : Self-motivated and motivational, self-starter, positive team player, adaptable, willing to travel 50 -75% of the time.

About us:
Asian Clinical Trials (ACT) is a full-fledged CRO providing complete solutions for global pharmaceutical, biotechnology and medical device companies in clinical research. ACT aims to maximize customer value by providing high quality, cost effective, professionalized services. Our staff strength, inclusive of the management team, senior functionaries and support personnel in the clinical operations, data management and administrative staff support provide a sense of our training, experience, and diversity we bring to the process.

Contact us:
Asian Clinical Trials
Serene Chambers
Rd #5 Avenue7 Banjara Hills
Hyderabad 500034 India

http://www.act-india.com/jobposting.htm
http://www.act-india.com/

[Admin]

Asian Clinical Trials Clinical Hyderabad Hyderabad : Clinical Research Associate
Company Name : Asian Clinical Trials Clinical Hyderabad
Company Location : Hyderabad
Designation (of vacancy) : Clinical Research Associate
Company E-mail ID : info@act-india.com
Company Website : www.act-india.com

Job Description, Candidate Profile, Company Profile, Company Address :

Candidate Profile :
Graduate or post graduate degree in life sciences, nursing or other health related science For e.g. BSc, MSc, BPharm, MPharm and MBBS
Company Profile :
Asian Clinical Trials (ACT) is a full-fledged CRO providing complete solutions for global pharmaceutical, biotechnology and medical device companies in clinical research. ACT aims to maximize customer value by providing high quality, cost effective, professionalized services. Our staff strength, inclusive of the management team, senior functionaries and support personnel in the clinical operations, data management and administrative staff support provide a sense of our training, experience, and diversity we bring to the process.
Company Address :
Asian Clinical Trials
Serene Chambers
Rd #5 Avenue7 Banjara Hills
Hyderabad 500034 India

[Guest]

CURRICULUM VITAE
NAME : kalpana gopagani
PLACE :HYDERABAD
Email id :kalpanag84 AT yahoo.in
OBJECTIVE :

. To be a successful pharmacist in pharmaceutical industry .To seek a challenging and growth oriented carrier that challenges creativity and gives me scope to apply my technical management skills and work towards the growth of the organization which in turns helps in boosting my career. My ambition is to be at the Top of the specialist in my field. I believe I possess the ability to race along in the track of achievers, turning all the stumbling blocks into progressive opportunities for the future, which I view as successful
Serial No. Examination Board/University Year of Passing Percentage
1 B.Pharmacy J.N.T.U University (H.I.T.S college of pharmacy ) 2010
73.2%
2. Intermediate
Sri chaitanya junior college
2006 89.8%
3. X Standard Don bosco high school
2004 85%
ACADEMIC PROFILE :
TECHNICAL SKILLS :
- Operating Systems : Windows XP,2003,MS Office
CO-CIRCULAR ACTIVITIES :
- Presented a poster presentation on the topic ”TRANSDERMAL DRUG DELIVERY DRUG PATCHES “ in HITS College of Pharmacy.
- I have participated in National Science Olympiad.
- Attended many motivational and personality development programmes.
PERSONAL SKILLS :
Sincerity, hard working nature.
- Good personality development skills.
- Building good rapport with team.
- Ability to cope up with new trends.
- Avid learner.
- I have attended soft skills session
ACADEMIC PROJECT :
Analagesic activity and anti inflammatory activity of ethanolic extract of oscimum sanctum
ACADEMIC SEMINAR :

Anti anxiety drugss

INDUSTRIAL TRAINING :
Industrial training, part of my undergraduate curriculum, in formulation, manufacture and quality assurance and quality control departments, exposed me to modern techniques in drug development, drug design.

[sampathgoud86]

June 04, 2011.

Dear Sir/Ma'am,

I am writing to apply for the Medical professional/officer position. I am enclosing a completed job application, my certification and my resume.

The opportunity presented in this listing is very interesting, and I believe that my strong technical experience and education will make me a very competitive candidate for this position. The key strengths that I possess for success in this position include:

* I have done my MBBS graduation from Osmania Medical College and Internship from the Osmania General Hospital and its allied hospitals wherein I was extensively trained by the professionals in all the practical aspects of clinical medicine and patient work-ups.
* I have successfully completed a call center training programme wherein I was well trained in things like Telephone etiquette, US and UK Phonetics, English grammar, Spoken English along with Communication and Presenting skills.
* I strive for continued excellence


With a Diploma in Computer Applications at an early age, I have a good understanding of the basics in Computers like MS DOS, MS OFFICE, C language, C++ and HTML. I also have experience in learning and excelling at new technologies as needed.

Please see my resume for additional information on my experience.

I can be reached anytime via email at sampathgoud86@gmail.com or my cell phone, .

Thank you for your time and consideration. I look forward to speaking with you about this employment opportunity.

[Guest]

Dear Sir/Mam,
I am interested in Clinical Research Associate job. I am , hereby, providing you my resume. Kindly, look into it.
NAME : Manasa Padmanabhuni
E-mail : manasampl AT gmail.com
Objective
To reach heights in the field of clinical research with educational and personal skills.
Summary of Skills
Highly optimistic person and flexible to all kinds of work schedules, good convincing skills and the capacity of analysing things critically.
Work Experience
Duration
Period
Organisation
Designation
Nature of Work
Educational Qualifications
1) Bsc Microbiology, Biochemistry, Chemistry from Aurora's Degree College, Hyderabad which is affiliated to Osmania University . the over all percentage of Bsc is 72.
2) Msc Clinical Research from ICRI, Bangalore which is in collaboration with Cranfield University, UK. The course will be finished by September of this year.
Projects
1)An interdisciplinary project on nanotechnology during sept 2007-January 2008 at Aurora's degree college.
2) Efficacy and safety of hypothetical Tri-Cyclic Anti-depressant MarQpin during March 2011-may 2011 at ICRI, Bangalore.

Additional Skills
Got Basic Computer knowledge
Achievements & Professional Activities
1) Participated in poster presentation competition in molecular life science held on 11th January 2007 at Aurora’s Degree College, Chikadapally, Hyderabad
2) Participated in IV short duration lecture program in modern biology sponsored by Indian Academy of Sciences, Bangalore on 13th-14th November 2006 held at ICSSR auditorium, Osmania University Hyderabad
3) Participated in the popular lectures on modern biology held on 15th Dec-2007 at CIEFL auditorium, Osmania University Campus, Hyderabad.
4) Participated in the National Seminars with the work on Nanotechnology on 11th January 2008 at Aurora’s degree college auditorium, Chikadapally, Hyderabad.

[Guest]

MANJUNATH P.Y
Mail ID : pymanju AT gmail.com
Profile :
To utilize my skills and activities in impacting the success and growth of clinical research group in becoming or sustaining its reputation as a leader in the clinical research industry
Key Skills :
- Excellent communication and presentation skills
- Excellent interpersonal skills
- Leadership skills and team player
- Ability to adapt and work flexibly in a new domain
Proficiency Skill Set ::
- Knowledge of Clinical Research & Regulatory Affairs.
Computer skills :
- Windows ’95, ’98, 2000, XP
- Applications : - MS Office Suite (MS Word & MS Power Point, MS Excel).
Education :
- Clinical Research& Regulatory Affairs from Manipal University Bangalore.
- Bachelor degree in Integrated Bio-technology from Gulbarga University in 2005-2008.
Subjects Specialized :
Clinical Research Methodology :
- Study design/methodology
- Research Protocol writing
- Preparing Case Report Form, Informed Consent Form, Survey questionnaire, Checklists, SOPs, Investigator Broucher, and
Regulatory Affairs in Clinical Research :
- ICH-GCP guidelines
- Nuremberg Code, Declaration of Helsinki and Belmont report
- FDA
- EMEA
- India-DCGI, Drugs and Cosmetics Act
Achivements :
- Active participation in the 2nd National Conference of Bio-technology
Interests and Activities
- Reading
- Playing and watching Cricket
- Watching Movies and Listening to Music

[Guest]

Ma.Cristina Garcia Dimitui
Email Add : mcdimitui AT yahoo.com
Formal Educational History
Last Date Attended Institution Name, Country Education Level/Degree Area of Study Completion Status
05/2006 Philippine College of Health and Sciences, Philippines Bachelor of Science in Nursing Nursing Completed
04/2010 Manila Central University, Philippines Bachelor of Science Medical Technology Completed
Employment History
Quintiles Employment History
Date of Employment : 02/2010 – Present
Handling 9 Sites (2 Protocol) for Diabetis Mellitus Type 2 Program
Job Title : Clinical Research Associate 1
Key Responsibilities : - Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and good
clinical practice.
- Provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas.
- Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to
manage ongoing project expectations and issues.
- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to
applicable regulations. Escalate quality issues to Clinical Team Lead (CTL) and/or line manager.
- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment,
case report form (CRF) completion and submission, and data query generation and resolution.
- Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by
submitting regular visit reports and other required study documentation.
- May provide assistance to more less experienced clinical staff.
Non-Quintiles Employment History
Date of Employment : 09/2009 - 02/2010
Name of Employer : Our Lady of Lourdes (COPD Trial)
Job Title : Clinical Research Coordinator
Key Responsibilities : Study Coordinator:
COPD Trial Phase III
Assisting the PFT of patients
Drug dispensing and accountability
AE’s, SAE monitoring, documentation at the site.
Updating clinical research database (electronic CRF).
Date of Employment : 04/2007 - 02/2010
Name of Employer : UERMMMC (Advanced Parkinson's Disease)
Job Title : Clinical Research Coordinator
Key Responsibilities : Study Coordinator:
Global Study in ADVANCED PARKINSON'S DISEASE
Phase III-A
Monitoring Vital Signs and Assessment to be reported to the Investigator’s.
Performs Tests, administer drugs needed, and operate specialized equipments assigned in the area.
Coordinates clinical research requirements, activities and investigation per department. Assess patient for protocol eligibility and communicate finding.
Updating and maintaining the clinical research database (e-crf)
Completes necessary documentation in accurate and timely manner.
Familiarize potential subjects each the details of the study through phone contacts and pre- study personal interview
Date of Employment : 09/2007 - 02/2010
Name of Employer : Philipppine General Hospital / The Medical City
Job Title : Senior Phlebotomist
Key Responsibilities : Senior Phlebotomist for Colorectal CA Phase I study.
For the Pharmacokinetic Study
Date of Employment : 09/2008 - 01/2010
Name of Employer : UERMMMC (Section of Neurosurgery)
Job Title : Private Scrub Nurse
Key Responsibilities : Private Nurse
Responsible for the instrumentation and neurosurgery system in the department. As one of their scrub nurse staff during major operation.
Date of Employment : 01/2009 - 06/2009
Name of Employer : NAtional Kidney Institute and Transplant ( Dialyisis Department)
Job Title : Clinical Research Coordinator
Key Responsibilities : QUICK STUDY OF DEPRESSION
Study in Depression Level of Patient underwent of the
Hemo Dialysis and Peritoneal Dialysis.
Date of Employment : 07/2006 - 06/2007
Name of Employer: Hi-Presicion Diagnostic Laboratory
Job Title: Laboratory Technician / Senior Phlebotomist
Key Responsibilities: Senior Phlebotomist
Handling clinical Trials Specimen.
Assisting Blood Extraction.
Clinical Trial Experience
Non-Quintiles Clinical Trial Experience
Study Phase: Phase 3
Indication: Neurological disease

Drug Class: CNS Degenerative Agents
Geographic Region: Asia Pacific
# of Sites: Large
# of Patients: Large
Role: Research Coord
Key Responsibilities: Study Coordinator:
Global Study in ADVANCED PARKINSON'S DISEASE
Phase III-A
Monitoring Vital Signs and Assessment to be reported to the Investigator’s.
Performs Tests, administer drugs needed, and operate specialized equipments assigned in the area.
Coordinates clinical research requirements, activities and investigation per department. Assess patient for protocol eligibility and communicate finding.
Updating and maintaining the clinical research database (e-crf)
Completes necessary documentation in accurate and timely manner.
Familiarize potential subjects each the details of the study through phone contacts and pre- study personal interview.
Study Phase: Phase 1
Indication: Cancer - Colorectal
Special Population: Immunocompromised Patients
Drug Class: Antineoplastic Agents
Geographic Region: Asia Pacific
# of Sites: 2

Role: Medical Technologist 1
Key Responsibilities: Senior Phlebotomist for Colorectal CA Phase I study.
For the Pharmacokinetic Study
Study Phase: Phase 3
Indication: Respiratory
Special Population: Elderly
Drug Class: Respiratory Agents - Bronchodilators
Geographic Region: Asia Pacific


Role: Research Coord
Key Responsibilities: Study Coordinator:
COPD Trial Phase III
Assisting the PFT of patients
Drug dispensing and accountability
AE’s, SAE monitoring, documentation at the site.
Updating clinical research database (electronic CRF).
Therapeutic Experience
Therapeutic Area: Neurology
Years Experience: 3 years
Indication: Neurological disease
Describe Experience: Performs Tests, administer drugs needed, and operate specialized equipments assigned in the area.
Coordinates clinical research requirements, activities and investigation per department. Assess patient for protocol eligibility and communicate finding.
Updating and maintaining the clinical research database (e-crf)
Completes necessary documentation in accurate and timely manner.
Familiarize potential subjects each the details of the study through phone contacts and pre- study personal interview
Relevant Training: Investigator's Meetings
Therapeutic Area: Oncology
Years Experience: 3
Indication: Cancer - Colorectal
Years Experience: 3
Describe Experience: As the Senior Phlebotomist Analyzing the Blood sample for the pharmacokinetics and local laboratory. Assisting the site coordinator to do some vital sign related task with the subject.
Department Specific Experience
Department: Clinical
Category Experience
Drug accountability Yes
ICF/study document development Yes
Initiation visits Yes
Management of SAEs Yes
Query resolution Yes
Site Contracting Yes
Study files maintenance Yes
Remote Monitoring Yes
Monitoring Visits & Source Data Verification Yes
Investigator Meeting Attendance Yes
Language(s)
Language Speaking Reading Writing
Tagalog-Filipino-Pilipino Fluent Fluent Fluent
English Fluent Fluent Fluent
Charter References: DR. AMADO SAN LUIS
NEUROLOGIST
UERMMC HOSPITAL
QUIRINO MEDICAL CENTER
ST.LUKES HOSPITAL AND MEDICAL CENTER
DR.ERMAN FANDIALAN
NEUROLOGIST- TRAINING OFFICER
DEPARTMENT OF NEUROSCIENCES
UERMMMC HOSPITAL
DR.ALFRED TAN
SECTION HEAD OF NEUROSURGERY
UERMMMC
DR. VLADIMIR HUFANA
SECTION OF NEUROSURGERY- TRAINING OFFICER
UERMMMC
DR FERDINAND E. TAN
Asst. Medical Director
Novaliches General Hospital
DR.SHIRLEY P. TAN
Senior Manager
Intercon Diagnostic Laboratory Inc.
MS. CATHERINE CHU R.M.T
OIC, Kalaw Branch
Hi-Precision Diagnostics Laboratory
DR. JOAN YABUT-DULFO
Dermatologist

[abhijith andipet]

Application for the post of CRA
Abhijith.A
Email :abhijithandipet AT yahoo.in,abijithclt AT yahoo.com
Career objective :
Seeking challenging career in the field of clinical Research were I get to learn effectively and working Sincerely There by developing the organization as well as my
Self.
Educational Qualification :
QUALIFICATION INSTITUTION UNIVERSITY
Professional Diploma In Clinical Research Catalyst Clinical Services Delhi
Bachelor in pharmacy Nandha college of pharmacy erode
Tamilnadu Dr.MGR Medical university Chennai
Higher Secondary Madavanandha Higher Secondary School ,Malappuram Kerala. Kerala State Higher secondary Examination
S.S.L.C Umbichi Hajee Higher secondary School ,Calicut. Kerala Kerala State Board of Examination
Trainings Attended :
- Undergone Inplant Training in Vyasa Drugs Pharmaceuticals Put Ltd, Cherthala, Kerala
- Undergone Hospital Training in Govt Hospital malappuram, Kerala.
- GCP Training by Quintiles and PPD
- Professional Diploma in clinical research Under catalyst Clinical services Delhi
Computer Knowledge :
Operating system : Windows 98, XP and Vista
Packages Known : Microsoft office
Data entry experience with Oracle , Rave and inform
Career Summary :
Worked as a Medical Representative at Cipla for 3 months
Currently working as a clinical research coordinator at Baby Memorial Hospital Calicut (3.5 year experience)
Familiar with ICH-GCP Guidelines,ScheduleY,Regulatory affairs ,Monitoring ,SAE and SAE reporting Timelines. Safety Notifications, Query resolution etc
Responsibilities
Coordination of all the Clinical Trials in Hospital
Preparation of Source Data
Data entry in eCRF or paper CRF and Query Resolution
Correspondence with EC for Submission ,approval etc
ICF Process with patient
Check the Study material accountability at site and order if needed
Drug Dispensing through IVRS and Perform the Drug accountability
Blood collection ,separation ,packing and Courier to Central lab
Maintain all the site files and Trial related documents
Prepare the site for Audit.
Research Experience :
1. Completed Trials
Theraputic Area/Indication Date Phase Position
Preventive Cardiology 2006-2008 III Coordinator
Hypertension 2008-2009 IV Coordinator
Blood sugar control in MI patients 2009-2010 III Coordinator
ACS 2008-2010 II Coordinator
DVT Prophylaxis 2008-2011 III Coordinator
DVT Prophylaxis 2008-2011 III Coordinator
Non Valvular AF 2007-2011 III Coordinator
Hyponatremia 2009-2010 III Coordinator
Hyponatremia (Extension Study) 2010-2011 III Coordinator
2. Ongoing Trials
Theraputic Area/Indication Date
Phase Position
ACS 2008 III Coordinator
Preventive Cardiology 2008 III Coordinator
Languages Known :
- Excellent communication skills in Hindi ,Malayalam, English and Tamil

[Guest]

CURRICULUM VITAE
N.sivakrishna
Email Id : nandyalasivakrishna AT gmail.com

CAREER OBJECTIVE :
Looking forward to a challenging and competitive work atmosphere leading to a Professional experience with a dynamic and progressive organization where my skills, talents and abilities will be utilized to the fullest for mutual benefit.
Educational Qualification :
Qualification Name of Institution Board / University Year of Pass out Percentage
%
BPHARMACY Deccan school of pharmacy, Hyderabad Jntu
2011
62.0
MPC Viveka junior College,
Tenali
Board Of Intermediate
2007
69.0
SSC Viswasanthi vidyaniktha,
Repalle
Board of Secondary Education
2004
72.0
DIPLOMA IN CLINICALRESEARCH : Rgulatory requirements
: Statitics in clinica research
: Clinica data management
: Clinisal trial management
: Clinical sas programming
: Pharmacovigilance
: 6-sigma practices in clinica research
Project Details :
Title : Formulation, development and evaluation of rosuvastatin
calcium oral floating tablets
Analytic method : Estimation of rosuvastatin calcium
Evaluation of tablets : Angle of repose
: bulk density
: compressibility index
: hardness,
: friability,weight variation
: in-vitro buoyancy studies,swelling characteristics,dissolution
Seminar :Environmental tobacco smoke and its determination in air
: Tobacco types
: Tobacco profile
: Determination in air
: Second hand smoke
DECLARATION :

I hereby declare that the above furnished details are true to the best of my knowledge and belief
Date: (Sivakrishna.N)
Place:

[Guest]

SHYAMA BHATTACHARYA

E-mail : cetrimide21 AT ymail.com

CAREER OBJECTIVE
To amalgamate my scientific and creative abilities and contribute in the domain of clinical research
I aspire to further my career by showcasing my potential for innovation and dynamic thinking

PROFESSIONAL EXPERIENCE
Feasibility Support Analyst : ICON Clinical Research (Bangalore) November 2010-Till present.
- Responsibilities include training and contacting site personnel (investigators and research coordinators) involved in clinical trials.
- Part of the core team for site feasibility assessment, using various online tools and tracking databases
- Providing ongoing support and training for the CRAs who are involved in various studies on each site, handling global CRA teams assigned on important awarded studies
- Analysis and interpretation of data for conducting site feasibility assessment by creating online questionnaires for investigators and generating reports using the responses received from the sites
- Made key contributions to projects by coordinating with CRAs and team managers on local and global level for executing strategies and process updates for the operations team.
Patent Analyst : Scope eknowledge (Chennai) October 2007-December 2009
- Handling and reviewing client queries for Patents in bio-molecular and allied fields.
- Patent and Non-Patent literature search in databases and filing reports to be forwarded to the client
- Preparing market survey reports and domain landscape reports
- Familiarity with current scientific literature and market research expertise
Lecturer : K.R.M.M.C (Chennai) August 2005- February 2006
- Instrumental in conducting and validating need for workshops
- Expertise in teaching Biochemistry and Molecular Biology
- Interfacing with senior management for assessing feasibility of research projects and standardizing
protocols for experiments

EDUCATIONAL CREDENTIALS
- PG Diploma in Clinical Research and Regulatory Affairs from Clinical Research and Management Academy (CREMA) Bangalore 2009 -2010
- M.sc Biotechnology from K.R.M.M.C (Madras University) 2002-2005
- B.sc Microbiology from Hindustan College (Madras University) 1999-2002
- Higher Secondary (C.B.S.E 12th) Kendriya Vidyalaya (I.F.F.C.O) Bareilly U.P
ACHIEVEMENTS AND HONOURS
- The main focus of my project was the study of complex surface attached bacterial communities known as “BIO FILMS” which grows on contact lenses, surgical implants and catheters
- Junior researcher in ASTRA ZENECA INDIA PVT LTD for a period of nine months (November 2006-August 2007) Involved in protein purification, running assays, in vitro protein synthesis, ELISA, Western Blot and PCR technique expertise
- Active member of the South Asian Federation Student Welfare Organization
- Won the second place in Pulse workshop on “Antimicrobial Susceptibility Test”
- Worked as a volunteer in Cancer Research Institute (WIA Adayar) (outpatient department) and gained relevant knowledge in patient diary maintenance, source document verification
HOBBIES AND INTERESTS
- Classical and western dance forms
- Astronomy
I hereby declare that all information mentioned above is true to the best of my knowledge.
Place : Bangalore Name: Shyama Bhattacharya

[Vijayrohit3@gmail.com]

I am Vijay Rohit. I have interested to work in CRO industries. I have fulfill to all of CR's knowledge. And I had also completed my M.sc.