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:
ยท Management of all clinical documents
ยท TMF oversight and reconciliation
ยท Management and maintenance of TMF
ยท Support cross-functional study teams by ensuring timely and effective project tracking and administrative support of clinical research studies
ยท Support clinical study managers and directors of clinical operations where needed
ยท Coordinate team and investigator meeting, take meeting minutes as needed
ยท Updating milestones on clinicaltrials.gov
ยท Coordinate the ordering and delivery of needed supplies such as lab supplies, drug supplies, etc. as needed
ยท Contribute to development of SOPs
ยท Participation in regular internal quality auditing of clinical study documents
Qualifications include:
ยท BA or BS in a life sciences field or healthcare, or a BSN
ยท 3+ years clinical research experience
ยท Knowledge of ICH GCP regulations, SOPS and internal tracking systems
ยท Effective interpersonal and communication skills
ยท Flexibility and adaptability within a highly dynamic clinical environment
ยท Ability to work independently as well as part of a team
ยท Ability to build and maintain successful professional relationships with vendors, other staff and investigators
ยท Experience with TMF maintenance and management
ยท 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?
