Translational Operations Associate/Sr. Associate

Full Time On-Site/Hybrid Operations Operations Associate Apply for this Job Remix launched with a vision to transform patient’s lives through modulation of RNA processing. Our breakthrough science provides a path to identify small molecules that impact the expression of disease driving mRNAs and proteins. We take on the challenge of addressing drug targets in diseases of high unmet medical need to bring new therapeutic options to patients. Remix has a commitment to demonstrate the highest levels of scientific integrity with urgency because those patients are counting on us to deliver. With an in-house technology platform built from scratch, we have rapidly generated multiple drug discovery programs that are advancing towards the clinic.

Position Summary:

The Clinical Biomarker Group is hiring a Translational Operations Associate/Sr. Associate who will be responsible for overseeing end-to-end sample tracking and logistics for clinical trial samples. This person will work closely with clinical operations, central laboratories and specialty lab vendors to ensure samples are shipped from clinical trial sites according to the lab manual and are received at the designated facilities. This individual will initiate analysis of samples according to the study sample analysis plan and ensure data is delivered in time for key internal and external meetings. This associate will serve as the primary point of contact for any clinical sample related queries and escalate as appropriate. This role requires someone who both understands the big picture of the overall translational clinical trial strategy and can focus on the detailed aspects of sample logistics needed to ensure sample and data integrity. Opportunity to broaden scope to include other operational activities such as drafting and reviewing lab related clinical trial documents such as lab manuals, study protocols and ICFs as well as contracting with specialty lab vendors and reviewing incoming data to monitor assay performance.

Principle Duties and Responsibilities:

• Oversee movement of clinical samples from clinical sites to specialty labs
• Execute on timelines for clinical sample testing and provide sample and assay status updates
• Primary point of contact for sample related queries
• Ensure all clinical sample related documents are filed and stored appropriately
• Monitor trends in sample quality as relates to clinical site sample collection and shipments

Qualifications:

• Bachelor’s Degree in scientific or related field
• Minimum of 3 years’ relevant (biomarker operations) industry experience
• Familiarity with clinical trial documents such as study protocol and lab manuals
• Knowledge of clinical trials and clinical sample management
• Experience working with external vendors/CROs
• Ability to work across functions
• Excellent verbal and written communication skills
• Strong attention to detail and problem solving abilities
• Ability to work as part of a team and also independently under general direction across several programs