Tiffanie Pederson has been working as a Senior Clinical Trial Manager at Alkahest, Inc. since 2018. Furthermore, this person has on-the-job experience at more than 19 companies using similar skills. Tiffanie has a total work experience of 18+ years. Tiffanie Pederson studied at the University of Phoenix from 2015 to 2017. Currently they live in New York, New York region. You can find Tiffanie Pederson's current phone and email with our search.
Name variants:
Tiffanie Pederson
Last updated Jun 22, 2024
Contact Information
Last Update
Feb 4, 2016
Email
tp**@alkahest.com, ti**@gmail.com
Location
New York, NY
Company
Workplace
Colleagues
Work History
Senior Clinical Trial Manager
125 Shoreway Dr SUITE D, San Carlos, CA
Lead Sr. Clinical Trial Manager for Alzheimer's Programs
from Aug 2018
Global Lead Clinical Trial Manager
1180 Veterans Blvd, South San Francisco, CA 94080
Rigel Pharmaceuticals, Inc. is a clinical-stage biotechnology company dedicated to the discovery and development of novel, targeted drugs in the therapeutic areas of immunology, oncology and...
Dec 1, 2015 — Aug 2017
Senior Clinical Research Associate
3201 Beechleaf Ct SUITE 600, Raleigh, NC 27604
Mar 2014 — Dec 2015
Clinical Research Associate Iii
11500 south Eastern Ave #240, Henderson, NV 89052
75% nationwide travel conducted monitoring visits and wrote reports in CTMS. Responsible for 21 sites and 8 protocols, monitored, tracked and managed all study related tasks and site trainin...
Aug 2011 — Mar 2014
Clinical Trials Manager and Study Coordinator of Clinic
New York
Managed all aspects of conducting Urology and Oncology clinical trials including: budget negotiations, contract/protocol review, recruitment, consent, patient scheduling, screening, enrollme...
Mar 2009 — Aug 2011
Lead Clinical Trials Coordinator
ÃÂâÃÂÃÂÃÂâAttends Investigator Meetings and organizes Interim Monitoring Visits with the sponsors Clinical Research Associates (CRAs).
ÃÂâÃÂÃÂÃÂâManages all aspec...
from Mar 2009
Senior Cllinical Data Manager
Lead Data Manager for Glioblastoma trials, 120 patients. Assumed overall responsibility for execution of the assigned projects, sponsor audits and database locks. Provided leadership and sup...
Jul 2008 — Jan 2009
Protocol Development Research Coordinator (Contractor)
ÃÂâÃÂÃÂÃÂâAssisted with the management of regulatory activity for sponsor protocols in accordance with GCP guidelines, the FDA, DHHS and OHRP regulations.
ÃÂâÃÂÃÂÃÂÃ...
Jul 2008 — Jul 2008
Sr. Clinical Data Manager
ÃÂâÃÂÃÂÃÂâTrained on all Lilly venture SOPs, documents and operating systems.
ÃÂâÃÂÃÂÃÂâLead Data Management contact for Lilly Enzastaurin/Glioblastoma trials, 12...
Jun 2008 — Jan 2009
Data Manager/Project Manager (Contractor)
ÃÂâÃÂÃÂÃÂâDeveloped all Data Management department standard operating procedures (SOPs), the Data Management Plan (DMP) and the Data Transfer Agreement (DTA). Worked with and m...
Feb 2008 — Jun 2008
Clinical Data Manager
Developed all Data Management SOPs, the Data Management Plan (DMP) and the Data Transfer Agreement (DTA). Implemented Data Management system into company structure. Acted as the project mana...
Feb 2008 — Jun 2008
Lead Clinical Data Manager/ Project Manager
ÃÂâÃÂÃÂÃÂâLead Oncology Data Manager and liaison between internal & clientsÃÂâÃÂÃÂÃÂàdata management, safety, biostatistics, regulatory and clinical project ...
Jul 2006 — Feb 2008
Lead Clinical Data Manager
Lead Oncology Data Manager and liaison between sponsor, safety, biostatistics, regulatory and clinical project team members. Oversaw data entry department, processed CRFs and completed data ...
Jul 2006 — Feb 2008
Lead Clinical Research Associate
211 Carnegie Ctr Dr, Princeton, NJ
In-house CRA Head Associate 100 international sites/ 60,000 patients, phases III and IV. Assisted in the development of: project plans, reference manuals, CRF guidelines and TMFs. Organized ...
Aug 2004 — Jul 2006
Clinical Data Coordinator (Contractor)
ÃÂâÃÂÃÂÃÂâWorked in Data Fax entering and verifying CRFs at levels 1 and 2 (Oncology, Neuropathy, and Ophthalmology).
ÃÂâÃÂÃÂÃÂâAssisted with 10+ client studies i...
Jun 2004 — Aug 2004
Senior Clinical Data Coordinator
Worked in Data Fax entered and verified CRFs (Oncology, Neuropathy, and Ophthalmology). Generated queries, updated database with resolutions, assisted in database locks and audits.
Jun 2004 — Aug 2004
Clinical Data Coordinator
ÃÂâÃÂÃÂÃÂâCompleted data entry and created queries for sites in Oncology studies.
ÃÂâÃÂÃÂÃÂâResolved database discrepancies, recognizing illogical and inconsisten...
Jul 2003 — Apr 2004
Clinical Data Coordinator
Completed data entry and created queries in Oracle and Oracle Clinical. Transcribed laboratory data including Hematology, Differential, Serum Chemistry and Cytogenetic Reports. Assisted in r...
Jun 2000 — Aug 2000
Education
2015 — 2017
2015 — 2016
2010 — 2012
2000 — 2004
1999 — 2000
Occupations
Coordinator
Doctor
Urologist
Investigator
Oncologist
HR Specialist
Recruitment
Professor
School Principal
Agents
Executive
Chief Executive Officer
Scientist
Biotechnology Professional
Manager
Managers
Physician
Medical Practice Professional
Medical Practitioner
School Administrator
Educational Manager
Corporate Executive
Chief Executive
Biologist
Biological Scientist
Operations Manager
Skills
Clinical Data Management
CRA
Study Start-Up
FDA Submissions
Data Base Locks
Query and CRF creation
Patient RecruitmentOncology
Osteoporosis
Urology
Neuropathy
CNS
Cardiovascular
Ophthalmology
Osteoporosis and Radiology Microsoft Office
Oracle
Oracle Clinical
Clintrial 4
3-4
5
ClinAccess Power Server 5
1
MedDRA
Data Fax
Phase-Forward: InForm Electronic Data Capture (EDC)
Integrated Review 4
Velos eResearch
Clinical Trials
Gcp
Cro
Therapeutic Areas
Clinical Research
Ctms
Good Clinical Practice
12 Years of Experience Working Within the Clinical Research Industry
Senior Cra
Cra Ii
Clinical Trial Manager
Senior Data Manager
Team Leadership
Protocol Development Regulatory Coordinator
Oncology Phase I Iv
Data Management