Contract - Senior Administrative Assistant, Regulatory Affairs

Location
San Francisco, CA, United States
Posted
Sep 19, 2020
Ref
891
Hotbed
Biotech Bay
Required Education
Masters Degree/MBA
Position Type
Full time
CONTRACT - SENIOR ADMINISTRAIVE ASSISTANT, REGULATORY AFFAIRS

Position Summary:

Provide primary administrative support to the Regulatory Affairs Department. Will also provide back-up support to other functions within the Clinical Development Organization.

Essential Duties and Responsibilities:
  • Provide administrative support to Vice President of Regulatory Affairs and his management team
  • Act as a central contact for the Regulatory Affairs team for designated project communications, correspondence and associated documentations (CDA, MDA, consulting agreements)
  • Setting up meetings and conference calls, often involving internal personnel and/or external parties, encompassing the use of audio and web-based meeting technologies
  • Act as a central contact for the Regulatory Affairs team for Finance PO requisitions and maintenance
  • Create agendas and take minutes for department/program, team meetings
  • Must be able to prioritize and manage multiple projects simultaneously
  • Maintaining day-to-day calendar and recurring meetings
  • Ability to work with minimal supervision
  • Handle confidential material with appropriate discretion
  • Serve as a collaborative member of the Clinical Development Organization administrative team and provide support/back-up, as needed

Meetings and Events Planning
  • Experience in conference and event planning and coordination
  • Experience in planning off-site meetings
  • Flexibility to travel to conference or meetings to provide onsite support

Travel, Expense Reconciliation and Interview Coordination
  • Seasoned in coordinating multi-leg domestic and international travels
  • Experience with CONCUR reconciliation (compile, submit, and track expense reports)
  • Experience with coordinating extensive recruiting efforts by working with human resources to schedule interviews
  • Experience with coordinating candidate interview packets which may include travel arrangements
  • Assist with New Hire, on-boarding activities

Qualifications:
  • A minimum of 8 years of administrative experience (biotech preferred) in increasing positions of responsibility
  • Ability to work in a fast paced, start-up environment
  • Flexibility with regard to job responsibilities and duties
  • Prior experience supporting Regulatory Affairs/Clinical Development preferred
  • Ability to multi task and shift priorities quickly
  • Strong knowledge of MS Office (Excel, Word, PowerPoint, Outlook, CONCUR)
  • Excellent analytical, planning/organizational skills with strong attention to detail
  • Ability to effectively communicate and share knowledge with internal and external contacts at all levels
  • Proven ability to work under tight deadlines and pressure in a composed manner
  • Must have excellent customer-service orientation, high degree of professionalism, and be a strong team player
  • Ability to learn quickly and take on new challenges as they arise
  • Must be flexible, resourceful, and detail oriented
  • Effective interpersonal and communication skills
  • Skilled in developing collaborative internal and external relationships
  • Proactive, efficient and timely follow through

Fit with GBT culture:
  • Ability to build strong relationships with co-workers of various backgrounds and expertise
  • Ability to function at a high level in a team setting whether leading the group or acting as an individual contributor
  • Values-based leadership consistent with GBT's Core Values
  • Excitement about the vision and mission of GBT
  • Flexibility
  • Integrity

NOTE: This position summary is not intended to be all-inclusive. Employee may perform other related duties as negotiated to meet the ongoing needs of the organization.

Global Blood Therapeutics is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status, or any other characteristic protected by law.