Job DescriptionThe Senior Clinical Trials Management Associate is a primarily an in-house sponsor position (although some travel is required) who will oversee multiple aspects of clinical trial conduct including study start-up, document generation and review, tracking of samples enrollment of study participants, and management of vendors.. The candidate must be knowledgeable of clinical research operations, including interpretation and implementation of FDA regulations/ICH guidelines. The position will report to a Senior Clinical Trials Manager of Clinical Operations.
Responsibilities include but, are not limited to:
Prepares and/or reviews study-related or essential study start-up documents as they relate to the supported clinical trials as delegated by the study manager (e.g., Clinical protocols, Informed Consent Forms, Investigator Brochures, Pharmacy Manual, Monitoring Plan, Laboratory Manual, Patient Diary, Clinical Site Procedures Manual, Pharmacy Manual, Case Report Form (CRFs), CRF Completion Guidelines and other relevant study plans and charters).
Works with multiple contract research organizations to communicate detailed timelines and ensure that transferred obligations and performance expectations are met. Provides corrective instruction, as necessary, when performance expectations are not being met.
Attends internal team and other meetings as required.
Provides training, as necessary, at investigator meetings and other trial-specific meetings such as site initiation visits and monthly teleconferences.
Creates and reviews site feasibility assessments required for study participation.
Manages and tracks key study deliverables such as screening, enrollment, biological samples and images, data flow and protocol deviations.
Proactively identifies potential study issues/risks and recommends/implements solutions; ensures issues are escalated as appropriate to Senior Manager.
Prepares metrics and updates to key deliverables for management.
Assists in the resolution of clinical trial queries and data review for interim analysis, primary analysis and final database locks.
Prepares site newsletters and other correspondence related to clinical trial conduct (eg, best practices and lessons learned, frequently asked questions) in collaboration with the study team
Assists in resolution of routine study questions from clinical trial sites in adherence to ICH GCP and the study protocol.
May lead less complex studies and/or manage components of more complex studies as a member of the study team
May participate in department initiatives or special projects, such as developing new tools or processes
Ability to coach less experienced colleagues in solving problems
Understands how decisions have an impact to the broader study goals
Other duties as assigned.
Basic Qualifications
BS/BA in nursing, science or health related field and 4 years of related experience – OR -
MS/MA in nursing, science or health related field and 2 years of related experience
Preferred Qualifications
Bachelor’s degree in nursing, science or health related field required with at least five years of related experience. At least three years of clinical trial experience with oncology, hematology or related therapeutic area experience considered a plus
Multiple years of experience managing the work of external candidates
Must be willing to travel at least 25% (possibly more)
Ability to manage time demands, incomplete information or unexpected events
Must display strong analytical and problem solving skills
Attention to detail required
Outstanding organizational skills with the ability to multi-task and prioritize
Excellent interpersonal, verbal and written communication skills are essential in this collaborative work environment
Comfortable in a fast-paced small company environment with minimal direction and able to adjust workload based upon changing priorities
Working knowledge of transplant patient care and apheresis collection a plus
The salary range for this position is:
Other US Locations: $115,260.00 - $149,160.00.Bay Area: $126,820.00 - $164,120.00.
Kite considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*.
For additional benefits information, visit:
https://www.gilead.com/careers/compensation-benefits-and-wellbeing
* Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.
Kite is a biopharmaceutical company engaged in the development of innovative cancer immunotherapies with a goal of providing rapid, long-term durable response and eliminating the burden of chronic care. The company is focused on chimeric antigen receptor (CAR) and T cell receptor (TCR) engineered cell therapies designed to empower the immune system's ability to recognize and kill tumors. Kite is based in Santa Monica, CA. For more information on Kite, please visit www.kitepharma.com. Sign up to follow @KitePharma on Twitter at www.twitter.com/kitepharma.
For Current Kite Pharma Employees and Contractors:
Please apply via the Internal Career Opportunities portal in Workday.
