Sr. Clinical Research Associate

EPM Scientific; San Francisco (FL); On-site; USD 10,000 - 125,000; Full time

Job summary

An established industry player in pharmaceutical manufacturing is on the lookout for a motivated Clinical Research Associate to join their dynamic team in San Francisco. This hybrid role offers the chance to manage and investigate clinical trials while ensuring compliance with ICH GCP guidelines. With a strong focus on growth and innovation, the company has made significant strides in the industry, achieving multiple product approvals since its inception. If you're passionate about advancing clinical research and eager to contribute to impactful studies, this opportunity is perfect for you.

Qualifications

• 2+ years of onsite monitoring experience at a sponsor or CRO.
• A working knowledge of ICH GCP guidelines is essential.

Responsibilities

• Manage and investigate clinical trials and post-authorization safety studies.
• Coordinate clinical monitoring and site management activities.

Skills

Clinical Monitoring

Site Management

Investigational Trials

Education

Bachelor's degree in Biological Sciences

Bachelor's degree in Nursing

Bachelor's degree in Pharmacy

Tools

ICH GCP guidelines

Job description

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

$10,000.00/yr - $125,000.00/yr

MUST BE LOCAL TO CA OR NY STATE - NO EXCEPTIONS

Company Summary: A global, specialty pharmaceutical group with an impressive track record is seeking a motivated Clinical Research Associate for a hybrid role at their San Francisco site. Their commercial supply of pharmaceutical products generated $83m in revenue in FY2023 (a 24% uptick from the year prior). Since their first clinical trials in 2006, they've had 3 approvals already on the market. Currently, they have 6 indications in Phases II and III, so they are looking for a driven, growth-oriented Clinical Research Associate to facilitate their in-house studies.

Responsibilities

• Managing and investigating clinical trials and/or post-authorization safety studies
• Performing and coordinating different aspects of clinical monitoring and site management
• 20-25% travel (1x a month)

Minimum Requirements

• 2+ years of ONSITE monitoring experience at a sponsor or CRO (academia does NOT count)
• A Bachelor's degree in Biological Sciences, Nursing, Pharmacy or a related discipline
• A working knowledge of ICH GCP guidelines

If you are interested in this Clinical Research Associate role, don't hesitate to reach out!

Seniority level

Associate

Employment type

Full-time

Job function

Research

Industries

Pharmaceutical Manufacturing