Is the Clinical Research Associate role remote?

Yes — Orca Bio lists this as a fully remote position.

What seniority level is this role?

Orca Bio targets mid-level candidates for this position.

Clinical Research Associate at Orca Bio

Joblaze summary

In the role of Clinical Research Associate at Orca Bio, the individual will monitor clinical studies to ensure compliance with protocols and regulatory standards, both on-site and remotely. Key skills include a strong understanding of clinical trial processes, regulatory requirements, and good clinical practice guidelines. This position is well-suited for candidates with experience in clinical research, particularly those familiar with biotechnology or cell therapies. The company is focused on innovative approaches to blood cancer treatment, indicating a commitment to advancing medical science.

Joblaze insights

Listed today on Joblaze — tracked directly from Orca Bio's career page.
Orca Bio has 53 other open roles including General Manager, Commercial Manufacturing Facility, Director/Head, Pharmacovigilance, Associate Director, Procurement & Materials.

Quick facts

Is the Clinical Research Associate role remote?: Yes — Orca Bio lists this as a fully remote position.
What seniority level is this role?: Orca Bio targets mid-level candidates for this position.

From the original posting

More than one million people in the United States today are fighting blood cancer. While a traditional allogeneic stem cell transplant has been the best hope for many, the transplant itself can prove fatal or lead to serious conditions, such as graft vs. host disease. Orca Bio is a commercial-stage biotechnology company redefining the transplant process by developing next-generation cell therapies with the goal of providing significantly better survival rates with dramatically fewer risks. With our purified, high-precision cell therapies we hope to not only replace patients' blood and immune systems with healthy ones, but also restore their lives. Summary of Role: In this Clinical Research Associate role, you will be responsible for monitoring the progress of clinical studies, either at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements. We are recruiting for two roles: one based on the West Coast and one based on the East Coast. Travel expected: ~1+ site visit per week, for sites that do not permit virtual monitoring.

Clinical Research Associate

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