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. …

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…

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…

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…

Job Description Job Description An opening has become available for a SCRA or CRA to join one of the fastest growing CROs. We are currently looking for a Clinical Research Associate to join us. This position is permanent, home-based, must be located in Washington/Oregon/ Colorado/Wyoming/Montana/Utah/Arizona/Idaho/Nevada/New Mexico . Senior Clinical Research Associate Job Description: As Clinical Research Associate you will be responsible for monitoring clinical trials and ensuring investigator…

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…

Job Description Job Description POSITION TITLE: Clinical Research Associate II DEPARTMENT: Monitoring Ora Values the Daily Practice of … Prioritizing Kindness * Operational Excellence * Cultivating Joy * Scientific Rigor At Ora, we are building the future of ophthalmic clinical research. As the world's leading full-service ophthalmic drug and device development firm, we guide our clients across all phases of clinical research to efficiently bring new products and therapies to market. Over the p…

Job Description Job Description Company Description PSI is a leading Contract Research Organization with more than 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications. Job Description As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, ma…

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…

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…

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…