CV, Curriculum Vitae and Online Resumes Search

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Online Resumes with "CRFs"

Experienced Research Professional seeks CRA position!

Passionate, hard-working, intelligent, leader, compassionate, organized

Ideal Companies: I would enjoy working with any CRO or Sponsor who values and rewards excellence and a strong work ethic from their employees.

Tags for this Online Resume: Clinical Research Associate, CRA, Regulatory, Monitor, Auditor, GCPs

CTA

Seeking for a challenging career in a progressive organization offering the opportunity for contributing my skills services to the organization and personal growth and to work sincerely with maximum effort using best talents and with a challenge to achieve required goals and targets, abiding to the decisions of seniors and to earn a good reputation what ever required.

Tags for this Online Resume:  Develop, maintain and manage appropriate study documentation,  Developing, writing and presenting the clinical trial protocols,  Initiate, maintain and reconcile Trial Master File.,  Monitoring the trial throughout its duration which will involve visiting the Study centers on a regular basis to check the patient data in the case report forms (CRFs) and to sort out any problems which may arise.,  Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other Data collection tools by careful source document review Monitor data for missing of implausible data.,  Complete Serious Adverse Event (SAE) reporting, process production of Reports, narratives and follow up of SAEs and managing the clinical data intermilitently as per 21CFR USFDA guidelines,  Monitor study sites independently according to protocol monitoring guidelines, S.O.P.s, GCP and ICH Guidelines.,  Independently perform CRF review; query generation and resolution against established data review guidelines on client data management systems as assigned Perform other duties as assigned by management., , maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned

Experienced Data Coordinator Relocating to Dallas, Texas

I am looking for a company where I can add to my extensive list of Data Coordinator skills as well as share my skills with others. Working for a company which fosters the expansion of knowledge, is constantly growing and supports its employees is very important to me.

Tags for this Online Resume: SAS, eDM, Oracle Clinical, DMP Composition, CRF Completion Guidelines Composition, External Data Reconciliation, Multi-tasker

Senior/ Lead Clinical Reseach Associate - over 15 years experience monitoring, site management, medical record review, training/mentoring junior CRAs. database locks. regional clinical team leader

My goal is to secure a regional, home-based position in which I can use my knowledge of all phases of clinical research to develop tools to collect data (CRFs/edit checks; to verify the data (site management/monitoring), clean data (database locks)and to insure patient safety by assuring all AE/SAEs are reported, protcols and infomed consent are IRBs approved and adherence to all ICH guidelines and regulations.

Tags for this Online Resume: Lead CRA, Data Manager, Sr. CRA, Regional CRA

Clinical Data Management,CT

To obtain a position where my diversified data management experience can be utilized in overseeing the entire data management process on clinical trial projects

Tags for this Online Resume: Team Lead, desgined CRFs, data validation specifications

Clinical Trials Associate

Michelle Straka, BSHS, CPT 1163 Portsmouth Circle Medina, Ohio 44256 Cellular: (216) 337-2007 Home: (330) 722-2165 Email: dodgestealthrt1994@yahoo.com Linkedin account: http://www.linkedin.com/pub/michelle-straka/1b/964/aa2 Objective Obtain the position of Clinical Research Associate to further advance monitoring career. About four years additional experience in research as a study coordinator, regulatory coordina...

Clinical Research Professional- 20 years experience- Memphis

Clinical research professional with over 20 years of experience in both industry and academia. Responsible for all audit activities for multiple phase 1-3 clinical trials. Responsibilities include but are not limited to ICH/GCP compliance. Reviews key study documents such as protocols, informed consents, CRFs, monitor reports, and CSR. Presents protocol and GCP training at Investigator meetings. Mentors and trains junior qu...

Tags for this Online Resume: GCP, FDA submission documents, Drug safety, GLP, NDA, Auditor

Clinical Research Associate

 John is detail oriented, highly dependable previous site monitor and study coordinator with 4 years and 6 months experience, including assistant project management in the pharmaceutical development industry  He has attained knowledge and experience in 4 years of hands on provision of care for elderly and disabled persons assisting them with activities of independent daily living as well as dealing with transitional aspec...

Ideal Companies: Alcon, Merck, Wythe, Pfizer, Bristol-Meyers Squibb, Covance

Tags for this Online Resume: in-house monitor, Clinical Research Associate

Clinical Research - 10 Years of Experience - Near 11801

Cover Letter Rupal brahmbhatt Respected sir/madam ,, My self Rupal Patel Brahmbhatt. I was working at Synchron Research Services a leading CRO of India. I have been the part of this organization from when it was established, and still I was working with the same organization from 12 years. I have been a part of more than 700 projects as well as clinical studies including USFDA submission projects. I have face the US...

Tags for this Online Resume: MS office, GCP, SOP, CRA, ICF, CRC

Clinical Research - 7 Years of Experience - Near m9w4v

COVER LETTER: Dear Sir/madam, It's my greatest pleasure to apply for the position of Research Assisatnt. I believe that my experience and skills will prove useful to your organization. I hope that you carefully review my qualifications and skills displayed in this letter and the resume attached to it. The amalgamation of my appropriate education and related experience has provided me with all the unique skills and qualifica...

Tags for this Online Resume: Transcription, Clinical Research, Documentation, Immunization, Management, Medical, Protocol, Quality Assurance

Clinical Research Associate

SUMMARY: To apply my knowledge of FDA Good Clinical Practice guidelines/ICH guidelines, extensive site/field Clinical Director, Site Lead Study Management, in addition to my experience with various therapeutic areas of medicine, to a position as a Clinical Research Associate. AREAS OF EXPERTISE * Management * Interview candidates and either make a selection decision or recommend individuals for hire. * Able to manage multip...

Tags for this Online Resume: Clinical Research, Research, Accounting, Acquired Immune Deficiency Syndrome (AIDS), Advertising, Amazon Elastic MapReduce, Audit, Basic First Aid, BLS, Budgeting