Clinical Trial Manager

EPM Scientific; San Francisco (CA); On-site; USD 130,000 - 160,000; Full time

Job summary

Join a fast-growing, science-focused company as a Clinical Trial Manager, where you'll oversee global clinical trials and ensure compliance with regulatory standards. This role offers a competitive salary, bonus opportunities, and the chance to work with talented colleagues on groundbreaking oncology therapies. With nearly $800 million in funding, this innovative firm is poised for success, providing you with high-level commercial exposure and the opportunity to make a significant impact in the field of clinical research.

Qualifications

• Deep knowledge of clinical trial regulations, especially in oncology.
• Experience managing clinical trials from start-up to closeout.

Responsibilities

• Collaborate with external vendors to ensure timely deliverables.
• Monitor trial progress and implement corrective measures.

Skills

Clinical Trial Management

Regulatory Compliance

Oncology Knowledge

Risk Assessment

Vendor Management

Veeva CTMS Proficiency

Tools

Veeva CTMS

Job description

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This range is provided by EPM Scientific. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$130,000.00/yr - $160,000.00/yr

Position: Clinical Trial Manager

Salary: $130,000-$160,000 + 15% bonus + pre-IPO equity

This company is founded and led by some of the industry's brightest, with their C-suite coming from companies like Merck. Many of their leaders were crucial to the development of Keytruda. They possess a proprietary drug discovery platform that has potential beyond one blockbuster drug, with applications in Oncology, Neurology, and Immunology.

With nearly $800 million in funding, they have a strong cash runway and a robust pipeline, including a phase 3 trial and 11 other indications in development.

The Clinical Trial Manager will be responsible for:

1. Collaborating with external vendors, including CROs, laboratories, and imaging providers, to ensure timely and effective deliverables.
2. Building and maintaining relationships with investigators, study coordinators, and site personnel to support patient recruitment and retention.
3. Monitoring trial progress, assessing risks, and implementing corrective measures to meet study goals and timelines.
4. Ensuring regulatory compliance with FDA guidelines, ICH-GCP standards, and other regulations.
5. Overseeing global clinical trial management, ensuring high-quality data within budget and timelines.
6. Leading trial start-up activities, including site selection, feasibility assessments, and documentation.
7. Developing operational strategies for oncology clinical trials.
8. Supporting site initiation, training, and monitoring for protocol and regulatory compliance.
9. Collaborating with cross-functional teams to uphold operational excellence.
10. Creating and reviewing study documents such as protocols, consent forms, CRFs, and SOPs.
11. Maintaining detailed study files and conducting regular reviews.

The ideal candidate should have:

• Deep knowledge of clinical trial regulations, especially in oncology, including ICH-GCP and FDA requirements.
• Experience managing clinical trials from start-up to closeout.
• Proficiency with Veeva CTMS.
• Understanding of oncology therapies, disease progression, and related terminology.
• Competitive salary and benefits.
• Opportunities for high-level commercial exposure.
• Work with talented colleagues in a fast-growing, science-focused company.

If interested in this role, please apply without delay.