May be responsible for CRA and CTAs as direct reports. ...
At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor. CRA’s are accountable for using their expertise to build and maintain the site relationship and ensure they are set up for success. As a CRA, Parexel will offer you world class technology and trainin...
Markets and promotes low- to moderate-income home loans.Seeks opportunities through seminars, home buyer education forums, and home ownership classes to emerging market populations and low- to moderate-income individuals.Establishes and cultivates relationships with community organizations, and othe...
At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor. CRA’s are accountable for using their expertise to build and maintain the site relationship and ensure they are set up for success. As a CRA, Parexel will offer you world class technology and trainin...
Through questioning the status quo and collaborating cross-functionally, the Manager, Clinical Operations provides leadership to a team of Clinical Research Associates (CRAs) and ensures the successful performance and delivery of his/her direct report’s project deliverables, on time with high qualit...
Specifically, the staff research associate will participate in the operation of instruments available at the Core Facility and provide sequencing-associated services, including but not limited to DNA/RNA extraction and quantification, setting up of Sanger sequencer, next-generation sequencing platfo...
The Clinical Research Assistant assists the Clinical Operations Team in a multi-functional capacity to carry out all assigned tasks associated with the collection, documentation, and maintenance of clinical data including phlebotomy/laboratory, data entry and administrative responsibilities. Velocit...
Lentiviral vector production and characterization for immune cell transduction in the vector engineering core lab.Develop and optimize methods to ensure high-titer lentiviral vector production.Provide technical support for process development, both internally and with external partners.Manage techno...
Roles on our site support the coordination and management of clinical research activities and involve working closely with research teams to oversee daily study operations and ensure compliance with all regulatory requirements. Provide guidance and training to clinical research staff. Assist with ma...
Avania is hiring Senior Clinical Research Associates (Sr CRAs) - West Coast - Extensive cardiology Class III device monitoring experience required. Avania’s ClinOps Team establishes, maintains and supports clinical trials; as a key member of the team, our Sr CRA performs clinical trial oversight for...
In Vivo (Senior) Research Associate - Contract - San Francisco Bay. Proclinical is seeking a dedicated and highly skilled (Senior) Research Associate to support the In Vivo Pharmacology Operations. In Vivo (Senior) Research Associate's. This role will play a crucial role in advancing all therapeutic...
Clinical Trial Manager / Senior Clinical Trial Manager. This role is a unique opportunity for an experienced Clinical Operations Professional with technical expertise in managing Phase I-III clinical trials in an industry setting and who has a strong knowledge of clinical operations, Good Clinical P...
Reporting to our Associate Director of Clinical Operations, the. Prepares and maintains documents and files such as clinical study files, regulatory binders, and operations manuals for clinical sites (i. Has some understanding of the science behind Clinical Research, observes and gains exposure to c...
Senior Clinical Research Associate. We are partnered with a rapidly expanding Neurology company in their search for a Senior Clinical Research Associate. This organization has already received multiple approvals for therapies generating upwards of 100 million dollars in revenue per year and they hav...
This role offers a unique opportunity for an experienced Clinical Operations Professional with technical expertise in managing Phase I-III clinical trials within an industry setting and a solid understanding of clinical operations, Good Clinical Practice (GCP), and FDA regulatory requirements. Hands...
The Clinical Trial Manager (CTM) is responsible for the day-to-day oversight of global clinical trials and will manage internal stakeholders, CROs, multiple service providers, clinical monitors, and clinical trial sites. This position will also work closely with a cross-functional team based in the ...
Through responsible research and development, we strive to be innovative leaders in biotechnology and regenerative medicine, renowned worldwide for our scientific and medical achievements and contributions to the health and well-being of communities. We have two business units, TheBioBox, which is f...
Develop expertise in assigned industries through independent and third-party industry research and targeted company research including analysis of public company filings. The research analyst position will be required to work out of either Miracle Mile’s Los Angeles, Sausalito or Chicago offices, wi...
Lead original research in foundation model and generative AI for automation. Collaborate with peers across research and product teams to foster innovation. Contribute to the broader application of your research within the company. Demonstrated excellence in research or significant product innovation...
Supports and coordinates clinical trial activities and manages execution of 1 or more clinical trials/programs to ensure completion according to timelines. They are looking to bring on a Clinical Trial Manager to the team. Ideal candidate will have at least 5 years of relevant experience in either s...
Staff Research Engineers/Scientists. Research and iterate models to ensure optimal-performance data transformation. ...
Assist the field Clinical Development team with administrative tasks for all clinical trials, including tracking study status and enrollment, managing research budgets, and maintaining up-to-date regulatory documents as required. Coordinate and organize clinical staff resources for internal research...
The Senior Research Assistant assists in entering and maintaining all documentation and records. Minimum two years of administrative/clerical experience required; one year research or laboratory experience preferred. Completion of LLU's educational program on "ethical use of human subjects in resear...
Minimum of 4 years of experience in clinical trial management, with a strong track record of leading Phase I-III trials. Are you a seasoned clinical trial professional looking for a new challenge? Join this dynamic and innovative biopharmaceutical company, where they are dedicated to transforming li...