The Masters of Arts in Clinical Counseling (MACC) Program invites applications for the Assistant Professor position starting August 2024. The California School of Professional Psychology (CSPP) at Alliant International University offers APA-accredited doctoral programs (PsyD and in Clinical Psycholo...
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...
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...
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...
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. Perform clinic...
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...
Please note: Only candidates with biotech/pharma industry experience will be considered.This organization is working on a novel approach using a non-viral targeted gene therapy to treat unmet needs.Perform extensive antibody screening and section, working with multiple tissue preparations and tissue...
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...
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...
Senior Administrative Assistant. Responsibilities include spearheading recruitment efforts, offering administrative support to our sales team, and assisting with various project-related tasks. ...
We are looking for an administrative and HR specialist!. ...
Medical, Dental, & Vision benefits. The Entry Level Non-Medical Caregiver provides services to patients/clients in their places of residence that includes, but is not limited to, certain hands-off care. ...
Our scientists, clinicians and Research & Dev Development, Research, Program, Associate, Operations, Chemistry, Technology. ...
Under the direction of the Chief Executive Officer (CEO), the Administrative Assistant (AA) I independently performs a variety of administrative tasks and special projects to assist the CEO in carrying out his/her duties and responsibilities. Relieving an administrator of assigned administrative det...
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. Associate Director, Project Management. ...
The Lead Administrative Assistant will primarily support the Executive Director and Project Team for Construction. Performs specialized administrative and general office activities in order to establish and manage the facilitation of administrative workflow within the department and/or unit. The Lea...
As a Clinical Research Coordinator I, you will work independently providing study coordination including screening of research participants for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Maintains research practices usi...
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...
Possession of a valid certificate from an agency approved by the Department of Consumer Affairs, Medical Board of California to practice as a Medical Assistant. Under the administrative supervision of the Supervising Registered Nurse (SRN) II/III, Correctional Facility (CF), and the clinical supervi...
The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Works closely with a regulatory coordinator or directl...
The Medical Assistant I (MA I) is an unlicensed healthcare professional who performs routine technical services within the medical practice settings under the supervision of the physician and the department’s leadership staff. Required: Basic Life Support (BLS); Medical Assistant Diploma. CHOC does ...
The Clinical Research Coordinator contributes to the overall operational management of clinical research/trial/study activities from design, set up, conduct, through closeout. Mathematical skills Sufficient to prepare clinical research budgets, knowledge of math ability and knowledge of clinical tri...
The Clinical Research Associate is the clinical sites’ direct point of contact and accountable for managing site quality and delivery from site identification through close-out. The Clinical Research Associate will oversee the conduct of the trial at designated sites, ensuring the rights and well-be...
A minimum of 12 months experience as a clinical monitor with demonstrated experience of monitoring (virtual or onsite). Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements. ...
Under the direction of Research Institute Management, the Clinical Research Nurse Coordinator II is responsible for providing coordinator assistance for sponsored clinical studies within the Center for Clinical Research in accordance with Institutional policy, Good Clinical Practice and ICH guidelin...