Research Assistant (copy)

Why work at Tilda?

Our mission is to accelerate clinical innovation. As a tech-enabled clinical trial network, we build software and services to help pharma innovators better execute their clinical trial programs. Our work leads to faster cures and thus institute a meaningful impact on millions of lives. You can help us realize that goal.

Work with some of the best researchers in the world: Our team of physicians and researchers are passion-driven, and have a long history of accomplishments. They have worked on hundreds of research studies, helping bring many new medical innovations to the market.

Join us at a magical time: We've hit revenue growth and product-market fit, which gives us a huge green field to work with. You'd join at the perfect time to shape what we build and how we grow. We are a Silicon Valley-based company, backed by leading venture capital and healthcare investors.

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Purpose of Position: *
Serve as liaison between Tilda Staff and the Site Principal Investigator(s), and Sub-Investigator(s).

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Responsibilities: *
1. Site preparation and ensuring site quality
2. Assisting with completing study visits
3. Maintaining and dispensing study product and supplies, through appropriate oversight by Clinical Research Coordinators (CRC) and Site Manager.
4. Completing and ensuring the quality of case report forms, electronic data capture (EDC) forms and information into the clinical trials management system (CTMS)
5. Processing and preparing laboratory specimens for shipment
6. Performing electrocardiograms (ECG) in the presence of Clinical Research Coordinators and study aligned clinicians
7. Ordering supplies from study aligned vendors
8. Inventory tracking in collaboration with on-site Clinical Research Coordinators (CRC)
9. Shipping supplies and labs to study aligned vendors.
10. Maintaining source documents (e.g. through digitization or completion of eSource in clinical trial management system).
11. Responding to queries in a timely manner (e.g. a liaison between the CRC and data entry team).
12. Filing of study-related documentation in CTMS and/or electronic Trial Master File.

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Education/Skill/Experience Requirements: *
Impeccable attention to detail and appreciates organized workflows
One to three years of experience in a clinical setting.
Familiarity with ICH/GCP principles

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Experience/Training: *
Phlebotomy and ECG experience preferred;
Bloodborne Pathogen and IATA Certification (shipping of dangerous goods) will be provided.
Proficiency with technology (G-Suite).
Lab Processing

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Definitions: *
CTMS - Clinical Trial Management System (CRIO)
eTMF - Electronic Trial Master File - SiteVault

For more information about Tilda Research, please visit https://tilda.bio/

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Perks*

• 401kHealth
• Vision, Dental & Life Insurance
• FSA’s
• Generous PTO
• Pet Insurance
• Paid Maternity and Paternity Leave

Our mission

Tilda exists to accelerate the development of new medical treatments by providing every person easy access to clinical trials. We do this through leading decentralized research technology and a caring team that always puts patients first.

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Reimagining clinical trials from the ground up*

We believe the future of healthcare will be powered by technology that gives all patients access to the best care. That starts with reimagining today’s complicated clinical trial process to make it more accessible for patients.

Tilda is championing a more diverse and inclusive clinical trial environment to help advance health equity. Pharmaceutical companies use Tilda to identify and enroll their ideal patients, and to run effective trials with precision. It’s now easier than ever to deliver clinical trials to patients, no matter where they live.

And we’re just getting started.

Job Type: Full-time