Agoura Clinical/Medical Research Job Listings

RDI - Clinical Operations Lead63844255182849120

Workable

RDI - Clinical Operations Lead

The Mission At RDI, we are building something most of the world thinks is impossible: A clinical trial engine that actually works — for the sponsors who need results, for the labs that generate data, and for the patients waiting on therapies. We sit at the intersection of clinical trials, laboratory operations, and highly specialized data systems — building trials that run faster, cleaner, and with fewer unforced errors, by closing the gaps that usually sink timelines. This is a company designed to build better systems for how trials are actually run. The Role We’re hiring a Clinical Operations Lead — someone who can both do the work and build the system. You will own trial execution — start to finish — while designing the systems that allow us to scale. You will mentor junior operators, work directly with sponsors, and stand between us and the thousand small failures that collapse studies. There is no giant department here. No safety net of redundant processes. If something breaks, you will see it. You will fix it. You will prevent it from happening again. You will work directly with the CEO and a highly driven cross-functional team. We are not looking for someone who wants a quiet management role. We are looking for a builder, operator, and coach who wants to create something that outlasts them. What You Will Actually Do Design and execute full clinical trial operations — protocol to closeout. Build the operational playbooks, systems, and SOPs we need to scale. Manage vendors, sites, CROs, and labs directly. Oversee enrollment, timelines, budgets, compliance, and data integrity. Train and mentor our junior team as they develop into full PMs. Sit across sponsors, labs, and internal teams to keep every trial on track. Solve problems that don’t yet have names. Build systems that make the next trial easier than the last. Who You Are You’ve run full clinical trials, from startup through closeout, with real accountability for timelines, vendors, and data. You’ve worked on the sponsor side, where the real accountability lives. You’ve built processes before — not just followed them. You are deeply familiar with GCP, ICH, IRB, site management, and clinical regulations. You can see around corners, spot operational risks early, and course-correct without drama. You love developing people and building team capacity. You write clearly, speak directly, and own your work. You are fully accountable — when things go wrong, you don’t point fingers; you fix them. Who You Are Not You’re not looking to “oversee” a team that does the work. You’re not afraid of ambiguity. You don’t need someone to hand you a 400-page SOP binder to get started. You don’t hide behind process when decisions need to be made. The Conditions Location: Los Angeles preferred. Remote considered for exceptional candidates. Travel: Occasional (site visits, internal meetings, vendor oversight)

Van Nuys, Los Angeles, CA, USA

Negotiable Salary

RDI - Clinical Research Associate63500033798787121

Workable

RDI - Clinical Research Associate

RDI is seeking a detail-oriented and motivated Clinical Research Associate (CRA) to join our dynamic team. As a leading organization in clinical research, RDI is devoted to advancing medical knowledge and contributing to the fight against diseases by conducting high-quality research studies. In this role, you will act as a critical link between the clinical sites and our research teams, ensuring that all clinical trials are conducted according to regulatory guidelines, protocols, and ethical standards. You will have the opportunity to work closely with investigators and other health professionals to monitor and evaluate study progress, data integrity, and patient safety. The ideal candidate will possess strong analytical skills and have a comprehensive understanding of Good Clinical Practice (GCP), clinical trial design, and regulatory requirements. You will be instrumental in ensuring the success of our studies by performing site selection, initiation, monitoring, and closeout visits. Join us at RDI, where you can make a meaningful impact on human health and work alongside passionate professionals committed to excellence in research. This is an exciting opportunity for those who thrive in a fast-paced environment and wish to contribute to cutting-edge clinical research. Responsibilities Conduct site visits including initiation, monitoring, and closeout activities to ensure compliance with protocol and regulatory requirements. Collaborate with investigators and site staff to provide training on protocols and study-related procedures. Review and verify clinical data for accuracy and completeness in accordance with Good Clinical Practice (GCP). Prepare and maintain necessary documentation, including progress reports, to keep all stakeholders informed about study status. Identify and resolve site issues, discrepancies, and non-compliance matters promptly to ensure study integrity. Assist in the selection and evaluation of study sites to ensure suitability for clinical trials. Manage study supplies and ensure timely delivery to clinical sites, maintaining an effective inventory. Requirements Bachelor's degree in life sciences, nursing, or a related field; advanced degree preferred. At least 2 years of experience as a Clinical Research Associate or similar role in the clinical research industry. Strong knowledge of Good Clinical Practice (GCP) and regulatory guidelines. Excellent communication, interpersonal, and presentation skills. Ability to travel to various clinical sites as required by the study protocol. Strong organizational skills and attention to detail in managing multiple priorities. Proficient in using clinical trial management systems (CTMS) and other relevant technologies.

Van Nuys, Los Angeles, CA, USA

Negotiable Salary

RDI - Clinical Data Manager63393501929091122

Workable

RDI - Clinical Data Manager

Job Title: Clinical Data Manager – Data Integrity & Analysis Own the data. Shape the science. About RDI RDI is a CRO purpose-built for diagnostics. Since 2008, we’ve completed over 200 trials supporting some of the largest IVD companies in the world. Our mission is to get better tests to market — faster — with cleaner data, smarter tools, and zero nonsense. We work at the intersection of research, tech, and regulatory strategy. If you care about meaningful data, and want to see your work shape real-world decisions, you’ll feel right at home here. The Role We’re looking for a Clinical Data Manager who does more than clean data — you think critically about how it's structured, how it will be analyzed, and whether it will hold up to regulatory scrutiny. You’ll sit between clinical operations and biostatistics, owning the entire flow of subject- and sample-level data. You’ll build eCRFs, validate inputs, spot errors others miss, and help shape how that data is ultimately analyzed and presented. If you’ve ever wanted to be both the person who finds the bad data and the person who can explain why it matters — this is that role. Key Responsibilities Build and optimize electronic case report forms (eCRFs) to simplify physician data entry and reduce protocol deviations Review, clean, and validate large clinical datasets (subject metadata, lab results, demographics, etc.) Flag inconsistencies, errors, and outliers with precision and context Format data to support downstream analysis (e.g., standardization, categorical formatting, units, date logic) Support basic statistical reporting (e.g., inclusion criteria tracking, diversity metrics, confidence intervals, ROC) Collaborate with our regulatory and science team to ensure final datasets support submission claims Partner with Salesforce developers and EDC platforms to improve the usability of our paperless trial systems Create reports that help us track site enrollment, sample quality, and trial performance in real time Ready to own the data — and the outcome? Join us and build something that actually matters. Requirements What You Bring 3+ years in clinical data management or diagnostics data analysis Strong Excel skills, plus familiarity with EDC platforms (Castor, Cloudbyz, REDCap, etc.) Exposure to basic biostatistics (even if not a statistician): sensitivity/specificity, AUC, stratification, etc. Ability to write queries, troubleshoot messy data, and explain your logic to both devs and scientists A mindset for structure, logic, and accuracy — you question the data before trusting it Bonus if you’ve worked with R, SAS, or Python to run analyses or QA data Even better if you’ve touched submissions to FDA or worked in regulated diagnostics Benefits Why This Role? You’ll have end-to-end ownership: from raw inputs to regulatory-ready datasets You’ll work across teams — clinical, lab, tech, and regulatory — with visibility and voice Your work won’t just live in spreadsheets. It will show up in FDA filings, strategic meetings, and patient-facing diagnostics

Van Nuys, Los Angeles, CA, USA

Negotiable Salary