Biosample Manager

As a Biosample Manager at Nurix Therapeutics, your primary responsibilities will include overseeing the lifecycle of clinical biosamples, ensuring compliance with protocols and informed consent, and managing vendor relationships. You will play a key role in coordinating sample processing, collection, and shipping, and will also participate in developing case report forms to capture biosample information.

To apply for the Biosample Manager role at Nurix Therapeutics, candidates should possess a B.S./B.A. in biological sciences along with a minimum of 5 years of relevant industry experience. Familiarity with FDA and ICH/GCP regulations, proficiency in MS Office, and a proven track record in sample and data management are essential.

The Biosample Manager at Nurix Therapeutics contributes significantly to clinical study success by providing operational leadership in sample management and ensuring that all biosample activities align with study protocols. Your role will help maintain smooth communication with clinical teams and investigator sites, which is crucial for efficient sample collection and compliance.

A successful Biosample Manager at Nurix Therapeutics should be detail-oriented with excellent organization skills to manage multiple priorities effectively. Strong communication skills are also vital for collaboration with cross-functional teams. Additionally, a proactive attitude and the ability to work independently in a fast-paced environment will enhance your effectiveness in this position.

Nurix Therapeutics encourages professional growth for Biosample Managers by providing access to training programs, the chance to collaborate with experienced professionals in the field, and opportunities to develop and refine standard operating procedures. Moreover, as a key member of the clinical study teams, you will have the chance to impact innovative drug development directly.

In managing multiple priorities as a Biosample Manager, I prioritize tasks based on project timelines and operational needs, utilizing project management tools to keep track of deadlines and responsibilities. Communication with stakeholders is key to ensure alignment and adjustments when needed.

To ensure compliance with FDA and ICH/GCP regulations, I make it a point to stay updated on current regulations and incorporate them into all aspects of biosample management, from protocol development to final reporting. Regular training and reviews of standard operating procedures also help maintain high compliance standards.

I have extensive experience working with laboratory vendors, where I've managed contract negotiations, coordinated technology transfers, and overseen sample processing. Establishing positive relationships with vendors has been essential for ensuring quality service and timely project execution.

Effective communication plays a vital role in my effectiveness as a Biosample Manager. It enables me to convey important information accurately to both internal teams and external partners, which is essential for facilitating smooth operational workflows and addressing any issues that arise.

I utilize various software tools to support data management and tracking within biosample management. Ensuring that all biosample information is accurately logged and routinely monitored allows me to identify trends and gaps quickly, which enhances our overall project performance.

My approach to training involves developing comprehensive training materials and conducting interactive sessions that address specific biosample procedures. I emphasize clarity and practical examples to ensure that study monitors and investigator sites understand their roles in the biosample collection process.

I assess the success of biosample management processes using metrics such as sample collection rates, turnaround times for processing, compliance rates, and feedback from site personnel. Analyzing these metrics helps identify areas for improvement and ensures we’re meeting study objectives.

One significant challenge I faced was coordinating timely sample shipments amidst unexpected delays. I navigated this by establishing open lines of communication with the shipping vendors, assessing alternative logistics options, and implementing contingency plans to minimize disruptions.

To ensure investigator sites can meet sample handling needs, I work closely with them during the planning phases to assess their capabilities and provide them with necessary training and resources, thereby aligning their practices with the study requirements efficiently.

SOPs are crucial for a Biosample Manager as they provide standardized processes that ensure consistency, quality, and compliance in biosample handling. They serve as a reference point for team members and help in training new staff, ultimately maximizing operational efficiency.