Associate Clinical Trial Manager

ABOUT US
CalibrSkaggs Institute for Innovative Medicines a division of Scripps Research is a firstofitskind nonprofit translational research institute dedicated to creating the next generation of medicines. CalibrSkaggs was founded on the principle that the creation of new medicines can be accelerated by pairing worldclass biomedical research with stateoftheart drug discovery and development capabilities. Scripps Research is ranked one of the most influential institutions in the world for its impact on innovation. Our educational and training programs mold talented and committed students and postdocs into leading edge scientists. Leveraging the unique scientific environment of Scripps Research impacting translational sciences CalibrSkaggs has created a portfolio of drug candidates and is shaping a new paradigm for advancing nonprofit biomedical research to impact patients while reinvesting in further innovative research. We expand basic knowledge in the biosciences and use these fundamental advancements to develop profound innovations that improve wellbeing. CalibrSkaggs drug development portfolio spans a broad range of human diseases including cancer autoimmunity and inflammatory diseases metabolic and cardiovascular diseases infectious and neglected diseases as well as agerelated and degenerative diseases. If you have a passion for making a difference this could be your opportunity to join our transformative team.

Position Summary

The Associate Clinical Trial Manager supports the internal Calibr Clinical team clinical site teams and CRO/vendor partners in of earlyphase clinical trials across multiple therapeutic areas. Focus on immunooncology and a wide range of programs covering neurodegeneration metabolic disorders autoimmunity and others. Assists in the of complex clinical programs participates in the design and planning of clinical studies and delivers successful operational outcomes across multiple Phase 1 and 2 clinical trials. The Clinical Trial Manager will apply their excellent operational capabilities as the main driver for project delivery within timelines and budget in accordance with the protocol while ensuring compliance with ethical and regulatory requirements.

Responsibilities and Duties

• Deliver operational excellence.
• Support coordination of clinical operations required to initiate execute and complete clinical trials to drive ontime delivery of milestones.
• Support Calibr Clinical team functions.
• Develop and maintain active clinical trial documents including protocols informed consent forms case report forms operational plans.
• Assist in setup and maintenance of clinical trial documentation including preparation for audits final reconciliation and archives.
• Conduct data review and assist in identification of data discrepancies while engaging vendors CROs and site personnel in resolution as needed.
• Monitor and/or comonitor clinical trials sites as necessary.
• Support audit activities including inspection readiness.
• Track investigational supplies specimens imaging.
• Support vendor selection and CRO activities.
• Collaborate with internal team members Contract Research Organizations and vendors on all deliverables.
• Perform all duties and responsibilities in accordance with CFR GCP/ICH Guidelines SOPs and other applicable guidelines.
• Contribute to process improvement initiatives departmental projects development and maintenance of Standard Operating Procedures (SOPs).

Position Requirements

• Minimum BA/BS or equivalent or relevant and qualifying training and experience.
• 1 years experience in clinical trial support operations or management experience at a biotechnology or pharmaceutical company or CRO; or other relevant research or project management experience.
• Ability and willingness for minimal travel (approximately 3 days every other month).
• Excellent leadership communication and organizational skills.
• Able to take initiative and communicate crossfunctional needs and expectations.
• Ability to proactively handle multiple tasks manage a diverse range of functional activities and solve problems.
• Strong communication and interpersonal skills.
• Highly responsive and proactive.
• Knowledge of CFR and GCP/ICH requirements.
• Experienced in Microsoft Office Products (Word Excel PowerPoint SharePoint Teams) and other clinical trial systems (e.g. CTMS EDC and eTMF).
• Strong problem resolution and conflict management skills.
• Attention to detail.
• Strongly Preferred: Oncology clinical trial experience.

PHYSICAL REQUIREMENTS

May include stationary position for an extended period of time traverse campus/facility as needed operate machinery such as computer phone copy machine exposure to cold or hot temperatures.

COMPENSATION

The expected hiring range for this position is $109000 to $115000 commensurate with experience. Consideration will be given to experience that exceeds the listed requirements.

COMPREHENSIVE BENEFITS INCLUDE

• Employer Contributed Retirement Plan Depending on eligibility employees receive an employer contributed retirement plan (no employee contribution required) and the option to contribute to a 403(b) (which is similar to a 401(k) using your own pre or posttax dollars)
• Full Suite of Health and Welfare plans including three medical plan options (including an HSA available option) dental vision life insurance disability EAP and more
• Access to Flexible Spending Accounts (Medical/Dependent Care)
• Competitive vacation and sick leave policies
• Free onsite parking

The above statements describe the level of work performed and expected in general terms. The statements are not intended to list all the responsibilities duties and/or skills required of employees so classified and the content herein is subject to change due to the business needs of Scripps Research with or without notice. Furthermore nothing in this job description shall be interpreted to be in conflict with or to eliminate or modify in any way the employmentatwill status of Scripps Research staff.

EEO Statement:
The Scripps Research Institute is an Equal Opportunity Employer. We promote diversity of thought culture and background in the fields of science. All qualified applicants are encouraged to apply and will receive consideration for employment without regard to race color religion sex sexual orientation gender identity national origin disability protected veteran status or any other legally protected characteristic or status.

Required Experience:

Manager