CV, Curriculum Vitae and Online Resumes Search

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Online Resumes with "source document"

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

I am MD by background with more than 5 years of clinical research experience

I am looking for a challenging job in a team-oriented environment.

Ideal Companies: Allergan, Genentech, Ista, Santen

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

Clinical Research Project Manager, Charlotte North Carolina

To acquire a mid level to managerial administrative position within the clinical research therapeutic field

Tags for this Online Resume: regulatory, data manager, project manager, quality assurance, auditor, monitoring, electronic data capture, GCP, research, eCRF, CCRP, human subject's protection, source documentation, study start up, primary outcome analysis

Human Resource Administration

Honest and reliable. Self-motivated with a positive attitude. Ability to work independently and as a member of the team. Energetic; outgoing; people person; excellent organizational skills; Type speed 40 WPM. Proficient in the use of all assigned office equipment, Microsoft and Macintosh.

Ideal Companies: VECO, BP, State of Alaska, Home Depot

Tags for this Online Resume: part time, work from home, human resource

Clinical Data Manager, 7 years experience

I am currently looking for work as a Clinical Data Associate, Data Manager or Data Coordinator. During my 7 years in the biotech industry, I have worked on all aspects of Data Management from the Data Entry process to the creation and implementation of the study documentation to the CRF and Database creation and implementation of Edit checks. I also now have a site perspective since my last experience was working directly w...

Tags for this Online Resume: Data Management, pharmaceutical, clinical research, oncology

Accountant

Accounting, Sales/Use Tax, Management jobs

Clinical Research Associate, seeking entry-level, in-house opportunity

I am an excellent candidate for a Clinical Research Associate position due to my unique combination of experience in Preclinical Research and Development, Pharmaceutical Sales, and CRA Training. In addition to the skills and accomplishments detailed in my c.v., please consider the following highlights: Certification from Barnett International (July 2012): 10-Week CRA & CRC Beginner Program. Coursework emphasized FDA reg...

Sr. Clinical Research Associate

I am looking for a position as a home based or office based Sr. Clinical Research Associate. I have been in the business 13 years, starting as a Regulatory Coordinator, then a Project Assistant, Clinical Assistant, and then a CRA. I have worked as a CRA for 2 years and as a Sr. CRA for 5 years. I have been home based for the past 5 years. I still enjoy the travel and working with my sites to submit clean data that refle...

Tags for this Online Resume: Experienced, Dedicated, Detailed

Registered Nurse, Clinical Research Coordinator, pharmaceutical trials, consultant, experienced

As my career goals are on target with my education and expertise, I am now seeking a non-traditional nursing role where my experience and education have provided me with knowledge in a wide range of areas with many prospects that require skills I have acquired over a long career. I am ready to move in a new direction using my passion for research, law, creativity, travel, information technology, consulting, advising and the...

Ideal Companies: Stanford, Amgen

Tags for this Online Resume: Registered Nurse, Research, Medical Records Reviewer, BSN, Coordinator , Consultant, Sales, Entrepreneur, Clinical Research Coordinator