Job Description Job Description Job Description: The Clinical Research Associate will support the execution and oversight of clinical studies across multiple indications and geographic regions, including the United States, Europe, and the United Kingdom. This individual will work closely with investigative sites, internal team members, and external partners to help ensure that clinical trials are conducted in accordance with study protocols, applicable regulations, Good Clinical Practice, and c…

Job Description Job Description Clinical Research Associate - Texas At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. As a CRA II at ICON, you will design and analyze clinical trials, interpreting …

Job Description Job Description Job Title: Clinical Research Associate (Must have oncology experience) Job Description This Clinical Research Associate role focuses on data management and clinic coordination for oncology clinical trials, with a balanced mix of patient-facing responsibilities and data-focused tasks. The position supports the full lifecycle of clinical studies by conducting pre-screening, recruitment, consenting, specimen coordination, and follow-up activities, while collaboratin…

Job Description Job Description Job Title: Clinical Research Associate Job Description This Clinical Research Associate role focuses primarily on data management and clinic coordination for clinical trials. The position supports the full patient journey within studies, including pre-screening, recruitment, consent, specimen collection, and follow-up, while collaborating closely with physicians and a small, tight-knit research team. The role requires frequent use of multiple electronic systems, …

Job Description Job Description Job Description: Job title: Research Associate Location: 445 Eastern Point Road, Groton, CT 06340 Duration: 6 months Pay Range: $42-$45/hr

Hiring: Clinical Research Associate (CRA), Medical Device | San Diego, CA Based fully onsite in San Diego CA with some domestic clinical site travel I'm partnering with a fast-moving, commercial stage medical device company running investigational device studies. The research here moves toward commercialization and patient impact rather than sitting in a lab for decades. What you'll do: Monitor multiple investigational device studies, both company-sponsored and investigator-initiated Run site…

InnoCare (HKEX: 09969; SSE: 688428) is a commercial stage biopharmaceutical company committed to discovering, developing, and commercializing innovative drugs for the treatment of cancers and autoimmune disease, with unmet medical needs worldwide. InnoCare has built up a fully integrated platform in terms of research and development, clinical development, manufacturing and commercialization. To date, the Company has developed a robust product pipeline comprising three approved drugs (orelabruti…

InnoCare (HKEX: 09969; SSE: 688428) is a commercial stage biopharmaceutical company committed to discovering, developing, and commercializing innovative drugs for the treatment of cancers and autoimmune disease, with unmet medical needs worldwide. InnoCare has built up a fully integrated platform in terms of research and development, clinical development, manufacturing and commercialization. To date, the Company has developed a robust product pipeline comprising three approved drugs (orelabruti…

The Clinical Research Associate will lead clinical studies and/or parts of studies. The associate will be responsible for leading clinical study activities and procedures. Duties also include execution of experimental protocols and specimen processing. Essential Duties and Responsibilities • Lead clinical research activities and study management. • Liaison with Clinical Services, Medical Director, Veterinary Director, and Clinical Consultants to lead special test requests and results delivery. …

Consultant, Clinical Site Lead, Medical Devices Summary Our client, a Fortune 500 Medical Device company, has engaged GForce Life Sciences to source a skilled Clinical Site Lead (CSL). The CSL will oversee clinical study site maintenance, data collection, and field monitoring to ensure compliance with protocols, regulations, and Good Clinical Practices. Responsibilities include managing essential documents, resolving data discrepancies, reviewing adverse events, and coordinating site initiation…

Job Description Job Description Senior Clinical Research Associate - Oncology - Knoxville, TN At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. What You Will Be Doing: Serve as the primary point of…

Job Description: Job title: Research Associate Location: 445 Eastern Point Road, Groton, CT 06340 Duration: 6 months Pay Range: $42-$45/hr

The Clinical Research Associate maintains Trial Master File (eTMF) and is responsible for its accuracy and completeness. Actively participates in start-up process regarding EC and RA submissions and may assist with ICF creation or update. Independently performs site evaluation/initiation, training, monitoring and closure visits and applies risk-based monitoring. Closely interacts with project team and is responsible for accurate and timely completion of reports, issues/deviation reporting and r…

1. Job Purpose: This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical study studies in accordance with Tigermed or sponsor Standard Operating Procedures (SOPs), International Conference on Harmonization Good Clinical Practice standard (ICH-GCP), Clinical Practice standard (GCP) and other applicable regulations; The position is responsible for ensuring that all data generated by the assi…

Position: Senior Clinical Research Associate (Sr. CRA) – Transfusion Medicine / IVD Location: Remote with around 75% travel Schedule: Monday–Friday, approximately 8:00 AM–5:00 PM CT Contract Length: 12 months with significant travel Travel: Expected to increase to approximately 60–75% as the study ramps up Position Overview: Our client is seeking experienced Senior Clinical Research Associates to support a high-profile, high-volume clinical study within its Transfusion Medicine group. This is a…

Company Overview Our client is a clinical-stage targeted oncology company committed to developing first-in-class and best-in-class targeted cancer therapies. They are advancing an innovative portfolio of therapeutics, supported by a leadership team with deep experience in the design, development, and commercialization of cutting-edge therapies, including antibody-drug conjugates. Position Overview The Contract In-house Clinical Research Associate (Sr. IHCRA) provides hands-on support for the da…

We are looking for a Freelance, Part-Time CRA located on the U.S. East Coast to support and strengthen our Clinical Operations team. Job Requirements: Bachelor’s degree required – preferred qualification in life sciences or medical sciences Minimum 3 years of experience of onsite monitoring activities Profound knowledge of clinical research processes and medical terminology Expert knowledge of ICH GCP, and international and local regulatory requirements Passion for clinical research English lan…

Kelly Science and Clinical FSP is currently seeking a Regional Clinical Research Associate for a long-term engagement in the US with one of our Global Medical Device clients. This person will join our Kelly FSP (Functional Service Provider) division, a managed solution provider and business unit of Kelly Services, Inc. This role is full-time and is offering full benefit options. As a Kelly FSP employee you will be eligible for Medical, Dental, Vision, 401K and a variety of other benefits to cho…

Remote Based The Sr. CRA supports the day to day operations associated with the execution of clinical trials. He / she will monitor multiple clinical trial sites and studies. The primary objective and purpose of this position is to ensure the overall quality of clinical trials by monitoring study data and managing site adherence to the protocol, GCP, all applicable regulations and related study documents. The Sr. CRA is the primary contact with the study site and serves as the liaison between c…

100% TRAVEL ROLE EST Candidates will have to travel sites located in Eastern Time zone. CST Candidates will have to travel sites located in Central Time zone. West Coast Candidates will have to travel sites located in West Coast Time zone. Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (Google Cloud Platform) and International Conference on Harmonization…