... 5/10 – 3/11 Takeda Pharmaceuticals (Delta-Pharma Contractor) Records Coordinator Prepare clinical
documents for archiving according to file retention schedule and Standard Operating Procedures (SOPs) including data entry of Trial
Master Files, ...
- Mar 06
Aliso Viejo, CA
... **** ******* **** ******** *** Tustin ***** ***-***-**** *******@*******.*** Clinical Trial
Assistant More than ten years of experience in Laboratory Research Universities. Expert Laboratory Assistant in Molecular Biology, Biochemistry, Microbiology ...
- Mar 06
... 07 – 6/08 Global Clinical
Operations – Johnson & Johnson (Janssen) Pharmaceutical Corporation, Raritan, NJ Contract Position as Administrative Assistant/Clinical Trial
Assistant • Provide administrative support to Director and Global Trial
- Mar 04
... a Clinical
Research Associate position with an organization that provides an opportunity to make a meaningful contribution and based on performance, obtain professional growth. QUALIFICATION SUMMARY: > Managed all aspects of a clinical trial
- Mar 03
... ISO 13485, ISO 14971, ICH guidelines Informed consent, IRB requirements, Ethical issues involved in clinical
trials, International and Multicenter Clinical trial
, CRFs, Packaging and Labeling requirements, Adverse events reporting European Union ...
- Feb 26
... STEP 3 : July 2011 (98) ECFMG Certified: January 2008 Certification Number: 0-709- 407-1 BCLS-ACLS : June 2012-2014 ABIM certified : 2011 BE- Rheumatology RESEARCH AND PUBLICATIONS INFLIXIMAB (Remicade) International Clinical Trial
for dosing in RA. ...
- Feb 09
... trials Conduct clinical
trials with major pharmaceutical companies Perform phlebotomy, vital signs, electrocardiograms, and neuropsychological scales Responsible for submission of applications to hospital IRB Maintenance of trial
documentation i.e. ...
- Feb 08
San Antonio, TX
research agreements, contract research organization service agreements and building and laboratory leases • Created US corporate standard operating procedure (SOP) for review and approval of nonpromotional scientific, clinical trial
- Feb 07
... http://www.linkedin.com/in/barbaraathomasenglish Career Focus Medical writing and translation Experience Summary • Experienced in writing medical review articles, reports of clinical trial
findings, conference reports, summaries, and website copy. ...
- Feb 06
... Have good understanding of Clinical Trial
process and various Phases in it. Comfortable working on Databases such as Oracle and MS Access. Good written and oral communications skills. COMPUTER SKILLS: Languages: SAS, PL/SQL, SQL, C++, C, PRO* C, ...
- Feb 04
... Experience San Jose Valley Research, Inc., San Jose, CA Jan 11 – Dec 12 Clinical Trial
Manager per project/ per contract RESPONSIBILITIES: • Accountable for site activities including site timelines, study visits, site selection, site initiation, ...
- Feb 04
... A valued partner with Clinical Trial
Operations, Global Regulatory Affairs, Quality Assurance, Global Trade Compliance, CROs, Logistics Providers and Clinical
Sites. Directs projects from conception to completion. Accomplishments Merck REsearch ...
- Feb 04
India, Chandigarh, CH
... > Knowledge of different databases related to Patents (WIPO, Espacenet, IPO, USPTO & many more country specific) & Clinical
Trials (clinicaltrials.gov, CTRI (IN), EUDRACT (EU clinical trial
Registry) & many more country & therapeutic specific ...
- Feb 03
... Methodological, legislative and ethical understanding of clinical
trials including clinical
protocol design, informed consent process, clinical trial
approval. IRB, preparation of study reports, case reports, monitoring trials, managing clinical
- Jan 31
... < PPD Project Assistant < Coordinated with the clinical
project team the distribution, retrieval and review of regulatory documents required for initiation or closeout of a clinical trial
< Assured currency of required clinical trial
- Jan 27
... of clinical
research studies. . Correspond with Investigators and pharmaceutical sponsors to ensure sites meet GCP-ICH guidelines, local regulatory requirements, and adhere to patient safety standards. . Experienced in several Clinical Trial
- Jan 26
Canada, Whitby, ON
... Service Technician - Performed installation, maintenance, calibration and repair of medical devices in support of a Phase III clinical trial
- Spearheaded the successful launch of the clinical trial
in Europe in 2004 - Created and delivered SOP and ...
- Jan 23
... *A Ashford, CT 06278 (609)***-**** firstname.lastname@example.org CURRENT POSITION Applied Clinical
Intelligence, LLC – Bala Cynwyd, PA Clinical
Data Manger - Contractor 2012-Present Responsibilities included: • Review of clinical trial
data in EDC ...
- 2013 Dec 13
... ICON Clinical
Research January 2006 – February 2007 North Wales, PA 19454 Clinical
Studies Associate • Assisting in study start-ups and maintenance of INDs for Clinical Trial
Studies for Pfizer. • Updating sponsor software systems Right Track II, ...
- 2013 Dec 12
... West Ashdale ( Philadelphia, PA 19120 Clinical
Research Associate Site Management & Initiation ( IND Submissions ( Protocol Review ( Quality Assurance ( Data Analysis & Monitoring ( Drug Safety Study Start-up ( Trial
Master File Auditing ( GCP & ICH ...
- 2013 Dec 10