Associate Director at bluebird bio
Winchester, Massachusetts
bluebird bio
Senior CTM
Cambridge, Massachusetts
Biogen
Senior Mgr, Clinical Operations Lead
June 2016 to June 2017
Cambridge, Massachusetts
bluebird bio
Associate Director
Family Action Network
Co-Chair, Community Connections
August 2013 to June 2014
Winchester, MA
Acceleron Pharma
Contractor, Clinical Trial Manager
March 2012 to June 2016
Cambridge, MA
Family Action Network
Volunteer, Chair of Newsletter
June 2009 to June 2013
Winchester, MA
Scientia Advisors
Contractor, Market Analysis
May 2007 to July 2007
Cambridge, MA
Wyeth Research
Intermittent Contractor, Bone Repair and Hemophilia
September 2005 to October 2006
Cambridge, MA
Wood Mackenzie
Senior Consultant, Life Sciences
2004 to 2005
Boston, MA
Wyeth Research
Senior Clinical Scientist
2000 to 2003
Cambridge, MA
Pharmaceutical Research Associates, Int'l
Lead Clinical Research Associate
November 1998 to August 2000
Shrewsbury, NJ
Merck & Company, Inc
Pharmaceutical Sales Representative
September 1996 to November 1998
West Hartford, CT
š Summary
Senior CTM @ bluebird bio Cambridge, MassachusettsSenior Mgr, Clinical Operations Lead @ Biogen From June 2016 to June 2017 (1 year 1 month) Cambridge, MassachusettsAssociate Director @ bluebird bio Co-Chair, Community Connections @ Family Action Network Responsible for overseeing community outreach programs for FAN members in Winchester and neighboring towns. Organize yearly clothing drive for Cradles to Crayons during the Christmas holiday season. From August 2013 to June 2014 (11 months) Winchester, MAContractor, Clinical Trial Manager @ Acceleron Pharma ⢠Responsible for overall study management of Phase I/II clinical trials, with up to 40 sites across the US⢠Lead a study team to ensure successful conduct of a clinical trial according to state and federal regulations and ICH/GCP as well as internal SOPs⢠Responsible for study conduct including maintenance of study timelines, subject recruitment, laboratory sample tracking, study drug supply, SAE tracking and monitoring report review⢠Assist in the development of Clinical Study Protocols, Informed Consent Documents, Protocol Amendments, Case Report Forms, and Study Plans⢠Assist with selection of contract research organizations (CROs), laboratory vendors, Interactive Response Technology (IRT) vendors, and other outsourced work, as well as oversee vendors during the course of a clinical trial⢠Provide support for overall clinical development strategy and program goals From March 2012 to June 2016 (4 years 4 months) Cambridge, MAVolunteer, Chair of Newsletter @ Family Action Network Responsible for oversight of committee members in publishing a bi-monthly newsletter for town members.Attend monthly board meetings and work with other committee chairs to be sure the newsletter is up-to-date with local kid and family friendly activities.Work with local businesses and non-profit organizations to encourage advertisement in the newsletter.Initially responsible for the layout of articles and ads at the back end of the newsletter.Author/contributor of parenting articles in the FAN Newsletter. From June 2009 to June 2013 (4 years 1 month) Winchester, MAContractor, Market Analysis @ Scientia Advisors Responsible for analyzing all start up companies with diagnostic tools in the area of Oncology. Participated in staff/client meetings and prepared power point presentations based on company needs and objectives. Some forecasting and market analysis also performed. From May 2007 to July 2007 (3 months) Cambridge, MAIntermittent Contractor, Bone Repair and Hemophilia @ Wyeth Research Reviewed and maintained central files with CRO in preparation for FDA audit (Bone Repair)Managed inspection preparations for EMEA audit (Hemophilia)Assisted with study start-up activities (Bone Repair) From September 2005 to October 2006 (1 year 2 months) Cambridge, MASenior Consultant, Life Sciences @ Wood Mackenzie Responsible for the development of strategies and solutions to business development opportunities for pharmaceutical and biotechnology companies.Lead projects from proposal writing through implementation and completion based on client objectives.Project tasks included brainstorming/strategy sessions with multiple team members and client personnel, analysis of market opportunities and forecasts, and writing of interim and final reports.Assisted with the development and growth of junior consultants. From 2004 to 2005 (1 year) Boston, MASenior Clinical Scientist @ Wyeth Research Performed tasks from study start-up through final report writing for various therapeutic areas within the Wyeth/Genetics Institute Organization (Bone Repair, Hemophilia, Oncology). Specific responsibilities included writing protocols and amendments, informed consent documents and study-site reference manuals, identifying and enrolling physicians for small and large clinical trials, identifying and managing contract research organizations for lab analyses, radiographic review and monitoring of clinical trials, leading project team meetings, reviewing and analyzing clinical trial data, identifying study costs, allocating expenses for trial materials and tracking investigator payments, organizing investigator-sponsor meetings, assisting with audit preparations for the FDA and EMEA and on-site monitoring of physicians participating in clinical trials. From 2000 to 2003 (3 years) Cambridge, MALead Clinical Research Associate @ Pharmaceutical Research Associates, Int'l Performed various tasks necessary for the conduction of clinical trials.Activities included conducting weekly CRA meetings, reviewing and tracking monitoring reports, maintaining sponsor study trackers, assisting project managers with sponsor-related objectives, participating in sponsor and investigator meetings, co-monitoring and training CRAs, training physicians, study coordinators and study staff on study protocols and monitoring of clinical sites. From November 1998 to August 2000 (1 year 10 months) Shrewsbury, NJPharmaceutical Sales Representative @ Merck & Company, Inc Promoted cardiovascular, osteoporotic, gastrointestinal and migraine pharmaceuticals.Participated in various team and physician meetings to educate and serve a client base (physicians, nurse practitioners and physicians' assistants). From September 1996 to November 1998 (2 years 3 months) West Hartford, CT
What company does Kristen Pappas work for?
Kristen Pappas works for bluebird bio
What is Kristen Pappas's role at bluebird bio?
Kristen Pappas is Senior CTM
What industry does Kristen Pappas work in?
Kristen Pappas works in the Pharmaceuticals industry.
Who are Kristen Pappas's colleagues?
Kristen Pappas's colleagues are Shannon Baumann, Erin Gleason, Meredith Willoughby, Crystal Russo, Erin MBA, David Seeberger, Michael Magee, Emily Pereira, Eli Pasackow, and Carolyn Ph.D
Extraversion (E), Intuition (N), Feeling (F), Judging (J)
1 year(s), 11 month(s)
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