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…

Purpose of the Role Responsible for the execution of protein science work plans within their area of expertise, supporting early drug discovery programs through the timely delivery of high-quality scientific outputs and technical solutions. Key Accountabilities Execute approved work plans in early drug discovery projects. Contribute to the optimization and continuous improvement of work plans by providing recommendations for review and approval Senior Scientists (Grade 5 or above) Support multi…

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. …

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…

Employment Type: Contract (Contract-to-Hire potential) Locations: Multiple openings — Northeast | Mid/Southwest | Midwest | Southeast Job Description: We're partnering with a private, global medical device company pioneering neurovascular solutions for stroke, aneurysms, and arteriovenous malformations. They've just received IDE approval for their first US Class III device trial and are expanding their clinical team to support site initiation and monitoring across a 35-site trial. Key Responsib…

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…

We are seeking a Senior CRA (Remote Contract with VERY MINIMAL TRAVEL – Less than 10%) for a successful and stable Molecular Diagnostics Sponsor . This Senior CRA to support Oncology Diagnostics studies . You will perform site start-up activities and visits (such as SQVs and SIVs), Site Monitoring Visits/IMVs (mostly remote visits), and related pre- and post-monitoring activities. This Senior CRA should be able to communicate with sites, deliver presentations, provide updates, and provide ongoi…

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. …

Purpose of the Role Responsible for the execution of protein science work plans within their area of expertise, supporting early drug discovery programs through the timely delivery of high-quality scientific outputs and technical solutions. Key Accountabilities Execute approved work plans in early drug discovery projects. Contribute to the optimization and continuous improvement of work plans by providing recommendations for review and approval Senior Scientists (Grade 5 or above) Support multi…

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…

Parexel FSP is looking for a CRA/Sr CRA in the US. Oncology Experience required. Cell therapy experience is strongly preferred. Job Purpose: The Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the local study team(s). The CRA works in close collaboration with other CRAs and the Local Study Team/ Local Study Associate Director (LSAD) to ensure that study commitments are achieved in a timely and efficien…

Parexel FSP is looking for a CRA/Sr CRA in the US. Oncology Experience required. Cell therapy experience is strongly preferred. Job Purpose: The Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the local study team(s). The CRA works in close collaboration with other CRAs and the Local Study Team/ Local Study Associate Director (LSAD) to ensure that study commitments are achieved in a timely and efficien…

Parexel FSP is looking for a CRA/Sr CRA in the US. Oncology Experience required. Cell therapy experience is strongly preferred. Job Purpose: The Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at allocated sites and is an active participant in the local study team(s). The CRA works in close collaboration with other CRAs and the Local Study Team/ Local Study Associate Director (LSAD) to ensure that study commitments are achieved in a timely and efficien…