Clinical Research Coordinator : Resume CV

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  1. Post Count Number #1
    Guest Poster
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    August 14th, 2008
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    Clinical Research Coordinator : Resume CV

    Dear Sir/Madam,
    I worked at Jehangir Clinical Development Centre Pvt Ltd (SMO) at pune as Senior Clinical Research Coordinator in oncology clinical trials since Dec 08.

    My total exp. in Oncology Clinical Research is 1 year and 6 months. Kindly find the attached CV herewith to consider my application for the suitable post at your esteemed organization.

    Thanking you.

    Yours Sincerely,
    Dr.Monali Thawkar

    CURRICULUM-VITAE :
    dr.monali_homeohelar AT rediffmail.com

    Interested in :
    Clinical Research(Data Manegment,Pharmacovigilance,.Safety and RA)

    Objective :
    An opportunity to work in a vibrant and exciting environment that hones my skills and to contribute positively towards the growth and prosperity of the company and also to secure a position in this ever-expanding field by virtue of my sincerity and dedication.

    Academia :
    - PGDCR & RA 2008 from Nucleus Pune Birmingham University U.K.
    - B.H.M.S. 2007-2008 from MUHS Nashik With 67%
    - H.S.C. 2001-2002 from Maharashtra State Board.

    Work Experience :
    1) worked as a Clinical Research Coordinator with various multicentric phase I, II & III oncology clinical trials at Jahangir clinical development center, Pune from 19 th Jan 09 till 15 th April 2010
    2) Citycare Hospital Nashik as a R.M.O. for six months in 2007
    3) Prasanna Paediatrics Hospital Nashik as a R.M.O. for three months in 2008
    4) Atharva Homeopathic clinic Nashik as a assistant doctor for three years (2006-08)
    5) Astha Homeopathic clinic Nashik as a assistant doctor from 2008-09

    Conceptual Skills :
    - ICH-GCP, Schedule-Y, ICMR Guidelines, Phase I, II, III & IV trials, Pharmacovigilance, Responsibilities of Monitor, CRA, CRC, Investigator, Sponsor, Informed Consent Process, CIOMS, IEC.

    Trial Related Experience :
    - Trained on ICH-GCP, Schedule Y, ICF Process, SAE reporting
    - Screening and Enrollment of study subjects.
    - Maintaining Site Master Files
    - eCRF and paper CRF filling.
    - Interactive Voice Respond System (IVRS) calling.
    - Study drug accountability.
    - Sample labeling and dispatching.
    - AE monitoring, reporting and follow up of study.
    - IEC/IRB correspondence including SAE submission, all essential documents.
    - Managing all trial activities including site initiation, sponsor visit, auditor visit etc.

    Sr. No. Trial Id Indication Phase :
    1 Piramal Serenity Advanced Refractory Malignancy I
    2 20050201 Ca NSCLC II
    3 0601 Ca NSCLC II/III
    4 PDX012 Ca NSCLC II
    5 20070307 Ca Colorectal II
    6 3144A1-203-WW Ca breast II
    7 05602 Ca SCLC II
    8 3144A1-201-WW Ca breast II
    9 20070782 Ca NSCLC III
    10 PAREXEL BIBF 1199.13 Ca NSCLC III
    11 AP23573-07-302 Metastaic Soft tissue or Bone Sarcomas Pivotal Trial
    12 CSTI571BIC08 Post op. patient of GIST III

    Strengths :
    - Comprehensive problem solving ability.
    - Flexibility to adopt to new technologies and zeal to learn new things.
    - Ability to work with minimal supervision in fast paced environment.
    - Can work in multicultural and different global work environment.

    Computer Skills :
    - Well versed with MS Office.Excel,Power Point,Internet,
    - Have worked on Internal Data entry software

    Conference Attended :
    - Workshop on “Global Clinical Research” on the 6th Nov 08 held at Manavta Cancer Hospital & Research Centre, Nashik.
    - Attended several Investigator Meetings and Site Initiation Visits.

    Extracurricular Activities :
    - Participated in State level Kho-Kho competition in 1999-00

    Personal Outline :
    -Date of Birth : 30 June1984
    -Marital Status : Married
    -Language Proficiency : English, Marathi, Hindi
    -Hobbies : Reading, Listening to music

    Declaration :
    I do here by declare that the information furnished above is correct and is true to the best of my knowledge

  2. Post Count Number #2
    Guest Poster
    Join Date
    August 14th, 2008
    Location
    Your Heart, Delhi
    Posts
    76,213

    Dear Sir/Ma'am,

    This is an official Application for clinical research post.
    I Dr . Poonam Pujari have done BAMS,practised for 9 years,then Post graduate Diploma clinical research is completed , working as CRC since 2 years. I'm very much intersted to work in your organisation.
    Kindly find attached my CV.

    Thanks
    Regards,
    Dr. Poonam Pujari

    RESUME :
    Dr. Mrs. POONAM SVIJAYKUMAR PUJARI
    E-mail ID :- poonampujari6 AT gmail.com

    OBJECTIVE
    :
    To make Career looking for challenging opportunity in the dynamic challenging & over expanding field of health care having huge untapped potential in our country, where I can put best of my knowledge and experience.

    EDUCATIONAL QUALIFICATION
    :
    Qualification Board/University Year of Passing Class:
    PGDCR OrangeLifesciences-Pune 2008
    B.A.M.S. Pune University 1998 Second
    H.S.C. Maharashtra State Board of Pune March 1993 1st Class
    S.S.C. Maharashtra State Board of Pune March 1991 1st Class

    OTHER QUALIFICATION :
    Currently Pursuing MBA-Professional (Exam Scheduled Dec 2011)

    Training Programme on R.C.H.
    :- Reproductive & Child Health

    COMPUTER KNOWLEDGE :
    MS-OFFICE
    Also exposed to internet Usage.
    E-mail ID poonampujari6 AT gmail.com

    CURRENT JOB WORK
    :
    Name of post :- Clinical research coordinator
    Pentagon Clinical Research Pvt. Ltd., Pune- Since 15 March 2010 till date.

    Working as Delegated CRC in following Trials :
    1. Phase IIb-Global Trial- Ulcerative Colitis
    2. Phase III- Global Trial- Pediatric Migraine
    3. Phase III- Global Trial- Acne Vulgaris
    4. Phase III- Global Trial- Atrial Fibrillation
    5. Phase III- Indian Trial- Anemia in pregnant women
    Phase IV- Indian Trial- Obesity
    Phase III- Indian Trial- Diabetic Mellitus Type II

    WORK EXPERIENCE
    :
    Name of Post :- Housemanship- In Pooja Hospital for 7 Months
    General Practice : - Since 9 Years upto June 2010

    EXTRA ACTIVITIES:
    WORKSHOP Attended at Sancheti Hospital
    Evidence Based Medicine & Medical Research
    In between 9 Years I have done practice for HIV patient for Corporatio Hospital.
    Monthly workshop for children vaccination since 3 years
    For workers free of cost consulting & medicine is Since 3 years
    Eye check-up camp
    Hepatitis-B Vaccination camp

    SCHOOL TIME ACHIEVEMENT
    :
    Karmaver Academy of Education-Rayat Shikshan Sanstha, Satara
    Certificate Awarded Exam for English Junior- Distinction
    Certificate Awarded Exam for English Senior- Distinction
    Certificate Awarded Exam for Math’s Subodha- Distinction
    Certificate Awarded Exam for Math’s Prabodha- Distinction

    STRENGTH :
    Hard Working & Sincere
    Better convenience Skills
    Better Management Skills

    INTEREST & HOBBIES
    :
    Gardening
    Traveling
    Social Work
    And Listening Music

    DECLARATION
    :
    I hereby declare that the all above mentioned information is true to best my Knowledge.

    DATE
    :
    PLACE : PUNE

    Yours Sincerely
    (Dr. Mrs. Poonam V Pujari.)

  3. Post Count Number #3
    Unregistered
    Guest

    Curriculum vitae for clinical research organization

    Dear Sir/Madam,
    I am working at P.D. Hinduja National Hospital & Medical Research Centre as Clinical Research Coordinator in Pulmonary medicine clinical trials since August 2012 to till date.

    My total exp. in Pulmonary Clinical Research is 10 months. Kindly find the attached CV herewith to consider my application for the suitable post at your esteemed organization.

    Thanking you.

    CURRICULUM VITAE
    SHILPA ASHWIN KORDE
    Email :korde.shilpa89 AT gmail.com

    Date of Birth : 6th August 1989
    Location : Mumbai
    Nationality : India
    Marital Status : Single
    Language Proficiency : English, Marathi, Hindi
    Hobbies : Reading, Listening to music

    OBJECTIVE :
    An opportunity to work in a vibrant and exciting environment that hones my skills and to contribute positively towards the growth and prosperity of the company and also to secure a position in this ever-expanding field by virtue of my sincerity and dedication.

    ACADEMICAL PROFILE :
    2012 M.SC MICROBIOLOGY (MUMBAI UNIVERSITY)
    2010 T.Y BSC MICROBIOLOGY (MUMBAI UNIVERSITY)
    2007 HSC (MAHARASTRA STATE BOARD)
    2005 SSC (MAHARASTRA STATE BOARD)

    OTHER SPECIALISATION
    “POST GRADUATE DIPLOMA IN CLINICAL RESEARCH MANAGEMENT AND REGULATORY AFFAIRS.”
    FROM HAFFKINE INSTITUE OF RESARCH AND VACCINE, PAREL, MUMBAI.

    Workshops and Seminars Attended :-
    Refresher GCP Workshop held by Quintiles in P.D.Hinduja National hospital and MRC.

    COMPUTER KNOWLEDGE :
    Proficiency in operating system windows and Ms-office.

    Interested Area to work :
    1. Clinical data management
    2. Pharmaco-vigilance.
    3. Clinical trials
    4. Safety and Regulatory affairs

    Strengths :
    - Good leadership skills as well as ability to work as part of a team.
    - Ability to work under stressful conditions.
    - Good Communication Skills and other soft skills.
    - Self Confident and a self-motivated person.
    - Quick Learner

    Work Experience :
    - working as a Clinical Research Coordinator with various multicentric phase III & IV pulmonary clinical trials under Dr. Zarir F. Udwadia chest physician (Principal Investigator)at P.D.Hinduja National Hospital and MRC from 20th August 2012 to till date.

    Trial Related Experience :
    ** Having experience of DCGI inspection for clinical trial.
    ** Completing regulatory documents
    ** Developing study process, documents
    ** Conducting Informed consent process.
    ** Having experience of enrollment process of patients for clinical trial and conducting patient visit according to study protocol.
    ** Having great proficiency in completion of eCRF and paper CRF filling.
    ** Conducting all research trials according to the ICH GCP guideline.
    ** Having experience of writing source note for each patient visit, conducting drug accountability for each study.
    ** Having great experience of IXRS call for IP dispensing.
    ** Collect data from patient examinations; prepare medical records for sponsor’s clinical report forms.
    ** Maintain extensive patient contact, via telephone and written correspondence. Monitor patients to track follow-up visits, record any adverse effects, and compile participant opinions on study in general.
    ** Reporting of Serious Adverse Event to the sponsor, the DCGI and the Institutional Ethics Committee.
    ** Maintaining Site Master Files.
    ** Sample labeling and dispatching.
    ** Conducting Site feasibilities.
    ** Site Initiation Visits
    ** Conducting monitoring visits.
    ** Attending the Investigators Meeting

    Experience in Clinical Trials :
    Idiopathic Pulmonary Fibrosis (IPF) – From August 2012 till to date(Sponsor pharmaceutical company- Boehringer Ingelheim)
    Multidrug - resistant Tuberculosis(MDR TB) – From September 2012 till to date(Sponsor pharmaceutical company- Otsuka)
    Idiopathic Pulmonary Fibrosis (PIONEER study)- From October 2012 till to date(Sponsor pharmaceutical company- Cipla pharmaceutical company)

    COLLEGE PROJECT :
    RESEARCH PROJECT ON Production of Biosurfactant from oil contaminated soil

    ANY ACHIEVEMENTS :
    I] WORK EXPERIENCE AS AN OBERVER AT (Certificates obtained)
    1) KEM HOSPITAL PATHOLOGY LABORATORY
    II] INDUSTRIAL VISIT TO BANGLORE
    1) SUTURES INDIA PVT LTD.
    2) UNITED BREWERIES- KINGFISHER
    3) MODERN BAKERY

    PROFESSIONAL INFORMATION :
    Work Experience : Since 10 months till date
    Current Responsibility : - Working as Clinical Research Coordinator
    Current Employer : P.D.Hinduja National Hospital and Medical Research Centre
    Current Annual Salary : 1, 44, 000 lacs per annum
    Expected salary : 2, 40,000 lacs per annum
    Preferred Job Location : Mumbai
    Desired Job Type : Full time permanent

    Declaration :
    I do here by declare that the information furnished above is correct and is true to the best of my knowledge.
    PLACE : MUMBAI