--- title: 'Senior Clinical Research Associate - Contract Position at ProTrials Research, Inc.' canonical: 'https://feeny.ai/job/senior-clinical-research-associate-contract-position-protrials-research-inc-505t6pkckxh7' type: 'job' last_seen: '2026-09-16' --- # Senior Clinical Research Associate - Contract Position at ProTrials Research, Inc. - **Company:** ProTrials Research, Inc. - **Location:** Regional - **Employment:** contract - **Work type:** remote - **Posted:** 2026-05-19 - **Last confirmed live:** 2026-09-16 - **Apply:** https://jobs.lever.co/protrials/f49d9cae-9b9d-4165-8172-a65ae28d43a6 ## Job description ProTrials is a women-owned, WBENC-certified Contract Research Organization (CRO) that has been a trusted partner in clinical research since 1996. Founded with a clear mission to deliver high-quality, experienced, and ethical services, we’ve supported research behind innovative treatments in the pharmaceutical, biotech, and medical device industries. Our people are the heart of everything we do. We believe great work happens when team members feel valued, supported, and empowered. At ProTrials, you’ll join a collaborative community committed to making a meaningful impact on global health. We are excited to connect with skilled individuals who share our passion for advancing clinical research with care, integrity, and excellence. ## ABOUT THE JOB ProTrials is seeking a Contract Senior Clinical Research Associate to join our team. The Contract Senior Clinical Research Associate (Sr. CRA) plays an integral part in the successful monitoring and management of clinical trials. Responsibilities of a Contract Sr. CRA include ensuring clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH GCP, and all applicable regulatory requirements. Contract Sr. CRAs may be required to travel up to 65%. HERE IS WHAT YOU WILL DO: - Monitor clinical studies of investigational and approved products that have been determined to satisfy a medical need and/or offer a commercial benefit, including qualification, initiation, interim, and close-out site visits - Manage and train site personnel on therapeutic area, protocol requirements, proper source documentation, and case report form completion - Manage and track the preparation and return of investigational supplies at individual sites - Monitor and document investigational product dispensing, inventory, and reconciliation - Monitor and document laboratory sample storage and shipment - Monitor trial by reviewing and reporting on the following: site enrollment and termination updates, monitoring visits, protocol deviations/exceptions, serious adverse events, and laboratory abnormalities - Review source data and case report forms for accuracy, completeness, and integrity of the data, and identify and resolve ongoing data issues - Review data queries and listings, and work with study centers to resolve data discrepancies - Review regulatory documentation for accuracy and completeness, and support study centers with regulatory issues - Maintain complete and accurate study files and review files to ensure all appropriate documentation is present - Maintain consistent and timely contact with the study centers, investigators, coordinators, client personnel, and other individuals involved in clinical trials - Serve as a resource for project team members including supporting CRA I and CRA II staff by providing solutions to resolve issues HERE IS WHAT YOU BRING TO THE TABLE: - RN or Bachelor and/or advanced degree in biological sciences or related field, or equivalent combination of relevant experience, education or training, and previous CRA experience demonstrating career growth in the CRA position - Detail-oriented - Excellent organizational skills, strong interpersonal and communications skills, and strong problem-solving skills - Flexibility with changing priorities - Ability to efficiently perform and prioritize multiple tasks - Familiarity with the medical and pharmaceutical industries, and related terminology and practices - Extensive knowledge of FDA regulations and their practical implementation - Ability to travel, including by air or by car on short notice - Proficiency in Microsoft Word, Excel, and PowerPoint Except as otherwise permitted or required by applicable law or regulatory requirements, ProTrials will retain the applicant’s personal information in accordance with its statutory obligations and internal policies and procedures. Information collected during application completion may be retained for a reasonable period of time and in accordance with the company’s established retention policies. Applicants seeking more information may contact HR@ProTrials.com. ProTrials is an equal opportunity employer. ProTrials is committed to providing a workplace free from discrimination and harassment. All qualified candidates will receive equal consideration for employment without regard to race, color, citizenship status, national origin, ancestry, gender (including gender identity and gender expression), pregnancy, and childbirth or related medical conditions (including genetic characteristics), genetic information, sexual orientation, age, religion, creed, physical or mental disability, medical condition, military or veteran status, marital status, political affiliation, or any other characteristic protected by state or federal law. ## About ProTrials Research, Inc. ## Company Overview - **One-liner**: ProTrials Research, Inc. is a woman-owned, full-service Contract Research Organization (CRO) that provides clinical development services to pharmaceutical, biotechnology, and medical device sponsors. - **Entity Type**: Private (bootstrapped; no public funding rounds disclosed) - **Headquarters**: Los Gatos, California, USA (with operations across North America and Egypt) - **Founded**: 1996 - **Founders**: Jodi Andrews (Founder and Co-CEO) ## Core Business - **Primary industry/industries**: Clinical Research / Contract Research Organization (CRO) - **Target customers**: B2B – pharmaceutical companies, biotechnology firms, and medical device manufacturers - **Mission or purpose statement**: “To provide the worldwide clinical research industry with professional services that demonstrate the highest level of experience, quality, and integrity while supporting career growth for our employees.” ([protrials.com](https://protrials.com/about-protrials/)) ## Products & Services ProTrials offers a full range of clinical development services: - **[Site Management & Clinical Monitoring]**: Oversight of clinical trial sites and remote/in-person monitoring. - **[Project Management]**: End-to-end trial coordination and milestone tracking. - **[Data Management]**: Collection, cleaning, and analysis of clinical trial data. - **[Biometrics]**: Biostatistics and statistical programming support. - **[Regulatory Support]**: Assistance with regulatory submissions, compliance, and ethics committees. - **Service Type**: Service-based (CRO), delivered both onsite and remotely. ## Market Standing - **Valuation/Market Cap**: Not publicly available (private company) - **Key Metric**: Annual Revenue ~ $27M (as of latest reports) ([linkedin.com](https://linkedin.com/company/protrials-research)) - **Notable Investors/Partners**: None disclosed; company appears bootstrapped and self-funded. Key clients include pharma, biotech, and medical device sponsors. - **Growth Signals**: - 97% company-wide retention rate (2025), 98% in clinical roles ([protrials.com/careers](https://protrials.com/careers/)) - Inc. 5000 honoree - Founders & Co-CEOs named PharmaVOICE 100 Most Inspiring Leaders in Life Sciences - Voted Silicon Valley Business Journal top 50 women-owned businesses - Employee headcount: 83 (LinkedIn) to 119 (Built In) – conflicting reports; LinkedIn shows -4% YoY growth ([builtin.com](https://builtin.com/company/protrials-research-inc)) ## Competitive Advantages - **Experience & Expertise**: Project team members average 10 years in the industry across numerous therapeutic areas. - **High Repeat Business**: Exceptionally high repeat business rate, reflecting service quality and client trust. - **Woman-Owned Certification**: Differentiator for sponsors prioritizing diversity in their vendor supply chain. - **Employee Retention**: 97% retention rate signals strong workplace culture and stability. - **Flexible Work Model**: Hybrid/remote options for many roles, appealing to a broad talent pool. ## Strategic Focus - **Current priorities**: Continue delivering high-quality clinical development services; invest in employee growth and retention; expand global reach through clinical operations personnel across North America and internationally. - **Growth direction**: Likely organic growth through client relationships and therapeutic area expertise rather than external funding. ## Why Work Here - **Culture**: Emphasis on collaboration, integrity, balance, and community giving. Core values include Foster Excellence, Connect with Passion, Act with Integrity, and Pursue Balance. ([protrials.com/about-protrials](https://protrials.com/about-protrials/)) - **Work Model**: Hybrid workspace – employees combine remote and on-site work. Many clinical roles offer remote options. ([builtin.com](https://builtin.com/company/protrials-research-inc)) - **Notable Benefits**: - Medical, dental, vision insurance - 401(k) with company match - Flexible paid time off (including company-recognized holidays) - Pre-tax flexible spending accounts - Family medical leave ([protrials.com/careers](https://protrials.com/careers/)) - **Growth & Training**: Job training and talent development programs; supportive environment for career advancement. - **Team Size**: Mid-sized CRO (83–119 employees) – offers a closer-knit, collaborative environment compared to large CROs. ## Sources 1. [protrials.com](https://protrials.com/) 2. [protrials.com/careers](https://protrials.com/careers/) 3. [protrials.com/about-protrials](https://protrials.com/about-protrials/) 4. [linkedin.com/company/protrials-research](https://linkedin.com/company/protrials-research) 5. [builtin.com/company/protrials-research-inc](https://builtin.com/company/protrials-research-inc) ## Other roles at ProTrials Research, Inc. - [Clinical Project Specialist](https://feeny.ai/job/clinical-project-specialist-protrials-research-inc-regional-t8t6m8ek9dc8) — Regional - [Clinical Project Manager - Contract Position](https://feeny.ai/job/clinical-project-manager-contract-position-protrials-research-inc-remote-qk5k9tw77zd1) - [Senior Clinical Research Associate](https://feeny.ai/job/senior-clinical-research-associate-protrials-research-inc-regional-58jjhh7wvwg7) — Regional - [Lead Clinical Research Associate - Contract Position](https://feeny.ai/job/lead-clinical-research-associate-contract-position-protrials-research-inc-remote-txhyfzz5y598) - [Lead Clinical Research Associate](https://feeny.ai/job/lead-clinical-research-associate-protrials-research-inc-remote-hx2h7v3sw0qw) - [Clinical Project Manager](https://feeny.ai/job/clinical-project-manager-protrials-research-inc-remote-0aqchz10jync) - [Senior Clinical Trials Associate](https://feeny.ai/job/senior-clinical-trials-associate-protrials-research-inc-regional-nvnsk8hf3wm8) — Regional