709 Results for

Chemical Engineering Jobs in Alabama

Jobs

Research Nurse IV, LPN/LVN, Clinical Trials Kaiser Permanente

Los Angeles, CA

Conducts and leads clinical research by: reviewing, designing, and collecting clinical trials data; leveraging an advanced knowledge of source data and the tools leveraged for analyzing, and interpreting clinical data; leveraging advanced knowledge when providing input on the design of clinical trials, studies, and interventions at the site-level; developing innovative clinical research protocols and other processes of large-scale clinical trials; preparing, submitting, and/or collaborating with others to ensure correct compilation of study documentation sent to regulatory bodies (e.g., IRB) for review and approval prior to implementation; may also be responsible for executing clinical trial activities (e.g., informed consent process, lab support and processing, pharmaceutical documentation data, sample processing, adverse event assessment process); and may be involved in various research lab operations (e.g., biological specimen collection, including patient preparation, labeling, handling, preservation or fixation, processing or preparation, and transportation and storage of specimens). Ensures documentation of clinical research files by: ensuring the timely, accurate, and complete documentation of all research activities (e.g., consent forms, reports, tracking forms); contributing to the development and/or implementation of moderately complex quality control and/or assurance measures and providing feedback to research staff and management; assessing volunteers and/or patients for eligibility to participate in Clinical Trials, escalating when necessary; and monitoring and auditing Clinical Trials across sites and presenting findings to KP leadership.

7 days ago

Research Nurse IV, Clinical Trials LVN (Durational with Benefits) Kaiser Permanente

Los Angeles, CA

6 days ago

Clinical Research Coordinator II - California Heart Center Cedars-Sinai Medical Center

Beverly Hills, CA

Primary Duties and Responsibilities: Establishes and executes logistical aspects of clinical research projects to achieve project objectives, including project planning, projecting resource requirements, and developing systems to ensure protocol compliance and patient safety. Coordinates administrative functions of research studies, including scheduling of patients for research visits, procedures, and labs, and completion and maintenance of consent forms, case report forms, SAE's, and source documents.

30+ days ago

Clinical Research Associate IRE

Long Beach, California

$91,336–$114,170 / year

Clinical Research Associate- Early Stage Development- West Region ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. Focus is early-stage development clinical trials (non-oncology)Key responsibilities include: Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.

30+ days ago

Clinical Research Associate II IRE

Los Angeles, California

$91,336–$114,170 / year

Willing and able to travel up to 50% for on-site monitoring visits across the West region; preference given to candidates residing in Los Angeles, Phoenix, Seattle, Denver or Portland, near major HUB airports to support efficient regional travel. Clinical Research Associate- Oncology- West Region ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

30+ days ago

Senior Clinical Research Associate IRE

Los Angeles, California

$110,520–$138,150 / year

Perform remote and on-site monitoring/co-monitoring visits (Site Qualification Visits, Site Initiation Visits, Interim Monitoring Visits and Close-Out Visits) to ensure data integrity and subject safety in the client's trials. Senior Clinical Research Associate- Oncology- Los Angeles, CA ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

30+ days ago

Clinical Research Assistant - Hematology/Oncology University of California

Los Angeles, CA

$26.23–$30.93 / hour

Major duties include, but are not limited to the following: triage paperwork, maintain confidential filing systems, confidential data entry, prepare and distribute correspondence, answer incoming phone calls, fax/photocopy/scan documents, scan lab manuals, update and distribute research charts and study logs, prepare investigational drug reports, obtain study participant records from internal and external sources, transport study participant records and charts to/from various CRU clinic locations, assist in obtaining physician signatures, assist with campus/building tours for sponsor representatives, process and pack/ship biological specimens (using dry ice), obtain liquid nitrogen and dry ice, request and prepare lab kits and supplies, dispose of biohazard material, review schedules for research coordinators and remind them of commitments, assist in tumor collection and freezing samples in liquid nitrogen, pick up oral medications from pharmacy, retrieve used oral medication for recording by research coordinator, attend meetings as required, perform other duties and assist as required. Ability to compose correspondence, prepare logs, and complete research forms/documents using clear and concise English grammar, Ability to compose letters and memos using clear and concise English grammar.

30+ days ago

Clinical Research Program Manager Charles R. Drew University

Los Angeles, California

$75,700–$90,000 / year

The Clinical Research Program Manager works closely with the Director, Principal Investigators (PI), ancillary departments, central research infrastructure teams, sponsors, institutions, and other entities as needed to manage the administration of all aspects of studies, including, but not limited to, compliant conduct, financial management, and adequate personnel support. Ability to develop and maintain professional working relationships in complex program/organizational settings involving heterogeneous constituents such as academic and clinical faculty, staff, students, and community partners from diverse backgrounds.

30+ days ago

Clinical Research Coordinator - Per Diem, Day Shift Adventist Health System

Glendale, CA

Applies substantial knowledge and experience to perform a wide range of advanced activities and/or determines how to use resources to meet schedules and goals; serves as working supervisor for team or work group. We are comprised of a 515-bed hospital, two urgent cares, home care services, comprehensive cardiology care and a vast scope of services located in the San Fernando Valley.

16 days ago

Clinical Research Coordinator II Velocity Clinical Research Inc

South Gate, CA

$30–$36 / hour

Implement and coordinate assigned clinical trials including start up, vendor management,subject recruitment, source development review, scheduling subjects, protocol training,collection of regulatory documents, conducting visits, ensuring data is entered in a timely manner and all queries are resolved, managing and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, providing all close out reports. Velocity Clinical Research is an owned and integrated research site organization, providing excellence in patient care, high quality data and fully integrated research sites.

27 days ago

Clinical Research Budgeting Analyst - Clinical Trials Providence St. Joseph Health

Los Angeles, CA

Remote

Main responsibilities include, but are not limited to, the review of New Study routing forms and essential study start-up documents, the itemized cost analysis and interpretation of clinical protocols into budget milestones, provide accurate patient cost descriptions for the ICF to be submitted to the IRB, and update budget, milestones, and ICF information as necessary per contract/protocol amendments. The Clinical Research Budgeting Analyst will be responsible for the timely and accurate preparation and maintenance of budgets for sponsored clinical trials, including the comparative review against budgets offered by study sponsors and the set-up of study payments milestones in the Clinical Trial Management System.

5 days ago

Clinical Research Budgeting Analyst - Clinical Trials Providence Health & Services

California, CA

Remote

$37.84–$58.75 / hour

It is comprised of eight hospital campuses (Ballard, Edmonds, Everett, Centralia, Cherry Hill (Seattle), First Hill (Seattle), Issaquah and Olympia); emergency rooms and specialty centers in Redmond (East King County) and the Mill Creek area in Everett; and Providence Swedish Medical Group, a network of 190+ primary care and specialty care locations throughout the Puget Sound. Main responsibilities include, but are not limited to, the review of New Study routing forms and essential study start-up documents, the itemized cost analysis and interpretation of clinical protocols into budget milestones, provide accurate patient cost descriptions for the ICF to be submitted to the IRB, and update budget, milestones, and ICF information as necessary per contract/protocol amendments.

5 days ago

Clinical Research Associate Zp Group Llc

$100,000–$140,000 / year

Keywords: Clinical Research Associate, CRA, Clinical Trials, Clinical Monitoring, Site Monitoring, Site Management, CRO, Biotechnology, Pharmaceutical Research, Oncology Research, Cardiovascular Research, Diabetes Research, GLP-1 Studies, Obesity Research, Ophthalmology Research, Clinical Operations, EDC Systems, CTMS, GCP, ICH Guidelines, FDA Regulations, Study Start-Up, Site Initiation Visits, Interim Monitoring Visits, Closeout Visits, Source Data Verification, Data Integrity, Protocol Compliance, Regulatory Compliance, Clinical Development, Trial Management, Investigator Relations, Multi-Site Studies, Patient Safety, Risk-Based Monitoring, Clinical Documentation, Drug Development, Research Compliance, Clinical Systems, Study Oversight. The Clinical Research Associate (CRA) will provide site management and monitoring support for clinical trials within Oncology, Cardiovascular, GLP-1/Obesity, Diabetes, or Ophthalmology research programs.

2 days ago

Coordinator, Clinical Research Consortia Children's Hospital Los Angeles

Los Angeles, California

$62,088–$82,784 / year
Part time

Overview: Purpose Statement/Position Summary: The Clinical Research Consortia Coordinator independently coordinate and manage all consortia activities at the coordinating center as it pertains to consortia protocols and clinical trials in conjunction with the Consortia Administrator and Medical Director. Children’s Hospital Los Angeles is consistently ranked among the top 10 children's hospitals in the nation, delivering world-class care through more than 350 specialized programs and services.

30+ days ago

Heart Institute - Clinical Research Associate I, Susan Cheng Team Cedars-Sinai Medical Center

Los Angeles, CA

Assists with regulatory submissions to the Institutional Review Board (IRB) and works closely with supervising research staff or directly with the Institutional Review Board to submit Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines. From genetic counseling and targeted drug therapies to a growing array of minimally invasive procedures, Cedars-Sinai continues to stand at the forefront of technology, innovation and discovery improving patient outcomes.

30+ days ago

Clinical Research Coordinator I/CPT - Women's Health Program - Inflammatory Bowel Disease Center Cedars-Sinai Medical Center

Los Angeles, CA

Verifies specimen identification, assesses appropriateness of test orders and quality of specimen by recognizing factors that affect procedures and results; takes appropriate action when corrections are indicated Identifies patients and patient samples by strict adherence to established procedures; labels samples accurately and completely. 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.

30+ days ago

Clinical Research Program Manager - Women's & Guerin Children's - Full-Time, On-Site Cedars-Sinai Medical Center

Los Angeles, CA

Collaborate with internal and external key stakeholders including other departments, leaders across the organization, representatives from external agencies/organizations in the management of the program to provide guidance, resolve issues, grow the program, and/or implement processes and/or solutions. You will be responsible for directing and managing specified programs and will provide leadership, guidance and direction for the day-to-day clinical research operations and activities, including authority to make independent decisions regarding program operations, administration, and governance.

20 days ago

Clinical Research Coordinator III - Cardiology Cedars-Sinai Medical Center

Los Angeles, CA

Provides study coordination for assigned projects, including patient screening and consenting, regulatory reporting, completion required data collection, maintenance of source documents, facilitation of all study logistics to ensure successful protocol implantation and patient safety. This includes managing schedules and coverage for the coordinator team, improving efficiency of research systems and processes, training of personnel, and resolution of day-to-day administrative and operational problems to ensure the successful implementation of research protocols.

30+ days ago

Heart Institute - Clinical Research Assoc I/CPT, Susan Cheng Team Cedars-Sinai Medical Center

Los Angeles, CA

The Clinical Research Associate I/CPT works under the direction of a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or other supervising staff to assist in tasks supporting the coordination/implementation of noncomplex research studies. Supports objectives of research studies through noncomplex tasks such as data collection, prescreening of potential and scheduling of current research participants, assisting in IRB submission activities, budget and billing, and ensuring overall compliance with all federal and local guidelines.

30+ days ago

RN Clinical Research, Full time, 8am-4:30pm PIH Health

Whitter, CA

$52.50–$84.25
Full time

The clinical trial nurse is required to have comprehensive knowledge in all areas of protocol design, strong clinical assessment and decision-making skills, ability to navigate fast-paced hospital environments, manage multiple studies, excellent communication and patient education abilities, knowledge of federal regulations (FDA, OHRP), ICH-GCP guidelines, and HIPAA, proficient in EMRs and clinical research platforms (e.g., Epic, REDCap, Medidata, OnCore). The fully integrated network is comprised of PIH Health Hospital - Whittier, PIH Health Hospital - Downey and PIH Health Good Samaritan Hospital, 27 outpatient medical locations, a multispecialty medical (physician) group, home healthcare services and hospice care, as well as heart, cancer, women’s health, urgent care and emergency services.

30+ days ago

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Chemical Engineering Jobs in Alabama

Research Nurse IV, LPN/LVN, Clinical Trials Kaiser Permanente

Research Nurse IV, Clinical Trials LVN (Durational with Benefits) Kaiser Permanente

Clinical Research Coordinator II - California Heart Center Cedars-Sinai Medical Center

Clinical Research Associate IRE

Clinical Research Associate II IRE

Senior Clinical Research Associate IRE

Clinical Research Assistant - Hematology/Oncology University of California

Clinical Research Program Manager Charles R. Drew University

Clinical Research Coordinator - Per Diem, Day Shift Adventist Health System

Clinical Research Coordinator II Velocity Clinical Research Inc

Clinical Research Budgeting Analyst - Clinical Trials Providence St. Joseph Health

Clinical Research Budgeting Analyst - Clinical Trials Providence Health & Services

Clinical Research Associate Zp Group Llc

Coordinator, Clinical Research Consortia Children's Hospital Los Angeles

Heart Institute - Clinical Research Associate I, Susan Cheng Team Cedars-Sinai Medical Center

Clinical Research Coordinator I/CPT - Women's Health Program - Inflammatory Bowel Disease Center Cedars-Sinai Medical Center

Clinical Research Program Manager - Women's & Guerin Children's - Full-Time, On-Site Cedars-Sinai Medical Center

Clinical Research Coordinator III - Cardiology Cedars-Sinai Medical Center

Heart Institute - Clinical Research Assoc I/CPT, Susan Cheng Team Cedars-Sinai Medical Center

RN Clinical Research, Full time, 8am-4:30pm PIH Health

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