FSP Clinical Trial Administrator
3 weeks ago
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
Essential Job Duties:
1) Document and track study activities using relevant forms and tools, as well as relevant Project Management Systems with guidance/support
2) Assist in the preparation of study and site specific materials in accordance with relevant SOPs
3) Complete minute taking and documentation for sponsor/external or internal teleconferences as requested
4) Assist in setting up and maintaining tracking systems/spreadsheet for e.g. study supplies
5) Maintain the Project Directory
6) Provide support for Investigator Meetings; track meeting attendees and/or other information regarding the Investigator Meeting
7) Provide support to project team (e.g. proof-reading and editing correspondence, mailings, shipping of study files, faxing and photocopying documents, assembling study documents, and arranging meetings, etc.)
8) Maintain Trial Master File documentation within the appropriate TMF platform, participate in TMF QC, as assigned, and track and /archive as applicable
9) Audit and CAPA tracking
10) Set up and maintain clinical investigator files and documentation
11) Liaise with vendors, as needed, for study conduct such as printing study materials and/or external systems access for study team members.
• Coordinate and plan study supply shipments with vendors
• Maintain and confirm shipment information such as courier tracking numbers and date of shipping and delivery
• Prepare/assemble/ship supplies to sites pre-SIV: Study File Notebooks, CRFs, other study-specific ancillary supplies (i.e. diary cards, patient visit reminders);
12) Generate reports as needed, for example CTMS site contact information list
13) Work with the In-House CRA and other project team members on reconciliation of data with CTMS.
14) General communications to sponsors, sites and internal team members via electronic mail or courier or telephone
15) Perform other administrative duties as assigned by Line Manager, Project Managers or Clinical Trial Lead.
Experience:
Minimum Required:
•Minimum one (I) year administrative experience or equivalent training
•Good oral and written communication skills
•Good organizational and time management skills
•Computer literacy (Microsoft Office Suite (Word, Excel, PowerPoint)
Preferred:
•Aptitude for handling and proof-reading numerical data, some spreadsheet softwarecompetency
•Good typing skills
•Good spelling and proof-reading skills
•Ability to operate standard office equipment (e.g., fax, copier)
•Works efficiently and effectively in a matrix environment
Fortrea is actively seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials. Our unwavering commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. Join our exceptional team and embrace a collaborative workspace where personal growth is nurtured, enabling you to make a meaningful global impact.
-
FSP Senior CTC(Beijing)
4 weeks ago
Pu Dong Xin Qu, China Fortrea Full timeDescription of Roles and Responsibilities • Trial and site administration : o Tracking (e.g. essential documents) and reporting (e.g. Safety Reports) o Ensure collation and distribution of study tools and documents o Update clinical trial databases (CTMS) and trackers o Clinical supply & non-clinical supply management, in collaboration with...
-
FSP SCRA I
4 weeks ago
Pu Dong Xin Qu, China Fortrea Full timeAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...
-
Clinical Program Lead, Immunology
3 days ago
Pu Dong Xin Qu, China 10287 GlaxoSmithKline (China) R&D Company Limited Full timeSummary: Responsible for integrating clinical development strategy with global considerations into strategic business decisions. Responsible for oversight of development and execution of studies linked to worldwide clinical development plans for assigned programs in assigned portfolio. Single point of accountability at clinical program level for the...
-
FSP CRA I
1 week ago
Pu Dong Xin Qu, China Fortrea Full timeAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...
-
FSP CRA I(Wuhan)
3 weeks ago
Pu Dong Xin Qu, China Fortrea Full timeAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...
-
FSP CRA I
2 weeks ago
Pu Dong Xin Qu, China Fortrea Full timeAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...
-
FSP-Sr. Statistical Programmer/Principal SP
3 weeks ago
Pu Dong Xin Qu, China Fortrea Full timeAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...
-
FSP CRA II
4 weeks ago
Pu Dong Xin Qu, China Fortrea Full timeAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...
-
FSP CRA II(Wuhan)
22 hours ago
Pu Dong Xin Qu, China Fortrea Full timeAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...
-
FSP CRA II(Wuhan)
2 days ago
Pu Dong Xin Qu, China Fortrea Full timeAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...
-
FSP CRA II
4 weeks ago
Pu Dong Xin Qu, China Fortrea Full timeAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...
-
FSPx SCRA
3 weeks ago
Pu Dong Xin Qu, China Fortrea Full timeEssential Job duties: The below statement are intended to describe the general nature of the job and are not intended to be an exhaustive list of all responsibilities, skills and duties. Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and...
-
FSPx CRA I(Wuhan)
4 weeks ago
Pu Dong Xin Qu, China Fortrea Full timeAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...
-
Business Development Director (China)
3 weeks ago
Pu Dong Xin Qu, China Fortrea Full timeAs a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access and technology solutions across more than 20 therapeutic areas. With over 19,000 staff...
-
Scientific Director, Precision Medicine
4 weeks ago
Pu Dong Xin Qu, China LabCorp Full timeAre you interested in making a real scientific impact through your everyday work? Would you enjoy working in a team-focused environment as you explore unique career opportunities? If you are looking for a company where you can personally advance healthcare and make a difference in peoples’ lives with your bold ideas and unique point of view, consider...