Job opportunity with a top Bay Area biopharmaceutical company that is looking for a Sr. CTA or to join their team!
Responsibilities will include but are not limited to:
· Management of all clinical documents
· TMF oversight and reconciliation
· Management and maintenance of TMF
· Support cross-functional study teams by ensuring timely and effective project tracking and administrative support of clinical research studies
· Support clinical study managers and directors of clinical operations where needed
· Coordinate team and investigator meeting, take meeting minutes as needed
· Updating milestones on clinicaltrials.gov
· Coordinate the ordering and delivery of needed supplies such as lab supplies, drug supplies, etc. as needed
· Contribute to development of SOPs
· Participation in regular internal quality auditing of clinical study documents
Qualifications include:
· BA or BS in a life sciences field or healthcare, or a BSN
· 3+ years clinical research experience
· Knowledge of ICH GCP regulations, SOPS and internal tracking systems
· Effective interpersonal and communication skills
· Flexibility and adaptability within a highly dynamic clinical environment
· Ability to work independently as well as part of a team
· Ability to build and maintain successful professional relationships with vendors, other staff and investigators
· Experience with TMF maintenance and management
· Organization skills, with a detail-oriented nature
Please apply here directly if interested but If you are genuinely not interested, is there someone you can recommend?
