Healthcare & Pharma Careers

Monitors patients on chemotherapy, immunotherapy, and cell therapy treatment trials and communicates determination of dose delays and dose reductions based on hematological as well as clinical criteria to treatment team.. Coordinates FDA documentation including collecting, de-identifying, and submitting serious adverse event documentation to protocol sponsor and oversight groups such as the Investigational New Drug Office or Clinical Research Organization.. Demonstrates knowledge of research process, Code of Federal Regulations and ICH Guidelines for Good Clinical Practice (ICH-GCP).. Demonstrates knowledge of the current NCI-Common Toxicity Criteria and institutional reporting requirements.. Preferred: Prior Research Nurse and/or Oncology experience.

Fertility Centers of Illinois is one of the nation's leading infertility treatment practices, providing advanced reproductive endocrinology services in the Chicagoland area for more than 30 years.. More In Vitro Fertilization (IVF) procedures than any other practice in the Midwest-more than 25,000 since 1997. The only infertility practice in the Midwest providing professional counseling from in-house, licensed, clinical psychologists and behavioral health specialists (Remove?). We are searching for a full-time (40 hours per week)Clincal Research Nurse for our River North location.. 3+ years of experience managing and submitting regulatory documentation for clinical trials (IRB/GCP/FDA)

Great opportunity for experienced Spanish Bilingual Clinical Research Coordinator or Research Assistant.. Play a major role in cutting-edge clinical trials - a meaningful healthcare position!. Obtain clean, objective, and accurate data within sponsor timelines while following applicable SOPs, policies and procedures, federal regulations, medical ethics, Good Clinical Practices (GCPs), International Council of Harmonization (ICH), Institutional Review Board (IRB) requirements, and in compliance with specific sponsor protocol requirements.. Their sites conduct Phase I-IV trials in therapeutic areas like cardiology, metabolic disorders, renal, CNS, pulmonology, and vaccines.. Preferably a minimum of 1 years experience as a CRC or RA, plus 1+ years' minimum experience within the field of clinical research or biological research in university.

Manages all elements of a clinical research trial in order to meet all protocol obligations while following applicable regulations; Code of Federal Regulations Good Clinical Practices (GCP) and International Conference on Harmonization GCP guidelines; state regulations and departmental/institutional standard operating procedures.. Here, Diversity, Equity and Inclusion are integrated into our core values and practices.. Practices professional nursing and promotes patient advocacy in accordance with the ANA Code of Ethics for Nurses and maintains a current Ohio Nursing LicenseCollaborates effectively and communicates patient care needs/expectations/priorities related to clinical trial participation to all involved care providers including unit nursing staff, attending physician, ancillary service providers (radiology, cardiology, physical therapy, pharmacy, etc.). to facilitate positive patient outcomes both in clinical care and in clinical trial participation Completes and manages all procedural, data, regulatory and training elements associated with clinical research project implementation, execution and close out to ensure participant safety, data integrity and compliance with all applicable regulations.. Certification by the Association of Clinical Research Professionals or Society of Clinical Research Administrators, preferred.

Quality Patient Safety Program Manager-Unity. With your expert knowledge of quality assurance, patient safety and risk management, and ability to communicate effectively, you will help us to create the safest and most welcoming environment for those we treat.. This role is based at and supports the Unity Center for Behavioral Health. The Quality and Patient Safety Program Manager is a pivotal role within our healthcare organization, responsible for integrating and overseeing quality assurance, patient safety, and risk management initiatives.. Comprehensive understanding of quality assurance, patient safety, and improvement principles, as well as regulatory standards.

Medical Device Auditors - Full-time - USA remote with extensive travel.. The Auditor, Medical Devices will support the Business Assurance business by leading and/or participating as an assessor during all phases of a client's management system, in accordance with the company's accredited certification program.. Travel will include overnight 3 to 5 days per week, to various worksites and client locations: This will be a remote/home-based position, with extensive travel to client sites required Travel will include overnight/multiple days, to various worksites and client locations Coordinate audit activity with team members Liaison with client regarding audit activity.. Minimum Requirements & Qualifications: 4 year college/university degree in a science or technical field (biology or microbiology; chemistry or biochemistry; computer and software technology; electrical, electronic, mechanical or bioengineering; human physiology; medicine; pharmacy; physics or biophysics) or equivalent combination of relevant education and work experience.. Training/experience in quality tools (Kaizen, lean manufacturing, etc

Collaborate with cross-functional teams, including R&D, production, and regulatory affairs, to support product development and production transfer activities.. Ensure that design controls are effectively applied throughout the product lifecycle, from concept to commercialization.. Prepare and maintain detailed documentation, including quality plans, inspection reports, and validation protocols.. Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities.. Relocation Assistance Provided: Yes

Clinical Research Associate 2064742 Location: Boston, MA (Onsite) Focus: Oncology Job Overview: Join our client as the inaugural in-house Clinical Research Associate to oversee quality and patient safety, coordinating with a CRO and facilitating daily study operations.. Build relationships with study sites and vendors, and develop monitoring tools for data review.. Primary Job Requirements: Bachelors degree with 6 years of clinical trials experience Skilled in managing complex oncology studies with a quality and compliance emphasis.. Willing to travel 50% and adept with Microsoft Office, EDC, CTMS, and eTMF. About Stratacuity: Whether you are seeking a career change or simply interested in becoming part of our network, you will appreciate the ethics guiding each Stratacuity team member.. We do not discriminate or allow discrimination on the basis of race, color, religion, creed, sex (including pregnancy, childbirth, breastfeeding, or related medical conditions), age, sexual orientation, gender identity, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, disability, status as a crime victim, protected veteran status, political affiliation, union membership, or any other characteristic protected by law.

Job Summary: Assists in the transition to a culture of safety by deploying proactive and preventive strategies to sustain fundamental improvements in the safe delivery of patient care.. Plans, organizes and assists in directing and implementing patient safety initiatives and patient advocacy through all CaroMont Health facilities.. Qualifications: Registered Nurse with Bachelor’s degree in nursing from an accredited college and current RN license to practice in NC. At least 1 year healthcare experience.. Experience in performance improvement process preferred.. Computer literacy, including use of Microsoft Excel and Word.

Signature HealthCARE is a family-based healthcare company that offers integrated services in 7 states across the continuum of care: skilled nursing, rehabilitation, assisted living, memory care, home health, cognitive care, and telemedicine.. Many of our skilled nursing facilities have achieved a 4 or 5-star overall rating from the Centers for Medicare & Medicaid Services.. Participate in Daily PPS meetings, weekly Medicare meetings, and month end meetings to assure federal billing requirements are met.. Our culture is built on three distinct pillars: Learning, Spirituality and Intra-preneurship.. Each pillar has its own staff and initiatives, ensuring that our unique culture permeates the entire organization.

Signature HealthCARE is a family-based healthcare company that offers integrated services in 7 states across the continuum of care: skilled nursing, rehabilitation, assisted living, memory care, home health, cognitive care, and telemedicine.. PINNACLE Workforce Development earn and additional dollar raise each year. At Signature HealthCARE, our team members are permitted no, encouraged to employ their talents and abilities to solve problems.. Our culture is built on three distinct pillars: Learning, Spirituality and Intra-preneurship.. Signature HealthCARE is an Equal Opportunity-Affirmative Action Employer Minority / Female / Disability / Veteran and other protected categories

Signature HealthCARE is a family-based healthcare company that offers integrated services in 7 states across the continuum of care: skilled nursing, rehabilitation, assisted living, memory care, home health, cognitive care, and telemedicine.. PINNACLE Workforce Development earn and additional dollar raise each year. At Signature HealthCARE, our team members are permitted no, encouraged to employ their talents and abilities to solve problems.. Our culture is built on three distinct pillars: Learning, Spirituality and Intra-preneurship.. Signature HealthCARE is an Equal Opportunity-Affirmative Action Employer Minority / Female / Disability / Veteran and other protected categories

The Department of Surgical Outcomes Clinical Research Coordinator will support clinical research activities for the department, division, and/or center.. As a result, the clinical research coordinator will help to advance research throughout the department and divisions as assigned.. This position will also support projects and assumes responsibility for the day-to-day operation of program activities, including the regulatory functions, project management, administrative tasks, study conduct, chart review, study enrollment, basic data analysis, RedCap, interpretation of results and reporting of research studies and experiments.. Completes Case Report Forms; responds to sponsor queries, prepares for internal and external audits by sponsor, IRB and/or the FDA/DHHS.. 1-3yrs Experience with facilitating research projects and regulatory functions, Clinical Research Certification (CCRP, CCRC) preferred

We are currently accepting applications for a clinical research nurse with expertise in caring for infants, young children, and school age children.. DBI provides advanced diagnostic imaging and multidisciplinary care for pregnant and postpartum individuals and families via clinical and applied research programs.. The clinical research nurse will participate in screening, assessment, recruitment, medical record extraction to support interdisciplinary studies.. This new position also will focus on conducting specific research related protocols, such as imaging and physiologic signals data acquisition (e.g. EEG, ECG), behavioral scoring, biosample collection and processing and related patient care for DBI infants, toddlers, and young children.. Outpatient services are provided in-person and via telemedicine, with the clinical research nurse located on-site at the main hospital campus in Washington DC.

Come join our team and make a difference as we blaze the way into the future of medical discovery through world-class clinical research.. Summary: PCR seeks a Clinical Research Coordinator who will be responsible for managing the day-to-day operations of assigned clinical trials, assisting in project planning, and ensuring that pre-established work scope, study protocol, and regulatory requirements are followed.. They will attend meetings and events to promote studies, recruit, and screen study participants, as well as document and report on the daily operations of a study and participant status.. The Clinical Research Coordinator I must be organized, excel at multi-tasking, detail-oriented, an excellent communicator, and be able to provide high quality patient care.. Benefits of working at Pinnacle Clinical Research: 401k Medical, dental, vision, long term disability, short term disability, FSA, and life insurance 3 weeks of paid time off 14 paid company holidays Tranquility Room (specific positions apply) Pinnacle Gym (specific positions apply) Scrub uniform voucher (specific positions apply) And more!

Prepare any necessary regulatory documentationDUTIES: The Clinical Trials, Billing, Budget and Compliance Specialist will report directly to the Senior Finance Manager.. Clinical Trials, Billing, Budget and Compliance Specialist will also work with faculty and staff to provide pre and post award support.. Choose from a wide variety of investment options through TIAA and Vanguard.. There’s always something going on at Penn, whether it’s a new exhibit at the Penn Museum, the latest music or theater presentation at the Annenberg Center, or the Penn Relays at Franklin Field to name just a few examples.. You can also enjoy substantial savings on other goods and services such as new cars from Ford and General Motors, cellular phone service plans, movie tickets, and admission to theme parks.

Join Kelly FSP as Senior Clinical Research Specialist with our Medical Device client in Irvine, CA!. This Senior Clinical Research Specialist will be responsible for supporting one or several clinical trials within the Clinical R&D Department while fostering strong, productive relationships with colleagues across the organization.. Serve as a Senior Clinical Research Specialist within the Clinical R&D Department to support execution of company sponsored clinical trials, ensuring compliance with timelines and study milestones.. May contribute to the development and delivery of appropriate global evidence generation strategies (EGS) and evidence dissemination strategies (EDS) within the assigned projects;. Minimum of a Bachelor’s Degree preferably in Life Science, Physical Science, Nursing, or Biological Science required.

Hims & Hers offers nonprescription products and access to highly personalized prescription solutions for a variety of conditions related to mental health, sexual health, hair care, skincare, heart health, and more.. The candidate will have experience in government affairs and public policy working in disruptive industries, telehealth, pharmacy regulation, or healthcare compliance.. Identify and engage with relevant working groups, advisory panels, and federal task forces to position the company as a thought leader in digital health and telemedicine.. Bachelor's degree in Public Policy, Political Science, Government Administration, Health Policy or other relevant field. Competitive salary & equity compensation for full-time roles

o Physicians are the Vanguard. As the Business Development Manager, you will serve as the primary customer-facing team member focused on driving market education of Profound Research capabilities and procuring clinical trials for our physicians and patients.. You will lead account planning and engagement, identifying ongoing and planned clinical trials which benefit from Profound's access to patients and our physician partner capabilities and expertise.. Conduct of market research identifying qualified opportunities to positively impact ongoing and planned clinical trials. The worker is required to have close visual acuity to perform an activity such as: preparing and analyzing data and figures; transcribing; viewing a computer terminal; extensive reading; visual inspection involving small defects, small parts, and/or operation of machines (including inspection); using measurement devices; and/or assembly or fabrication of parts at distances close to the eyes.

We are seeking a highly skilled and dedicated Director of Nursing to join our team at Kith Haven.. Staying current with managed care, Medicare, and state Medicaid regulations. Participating in Quality Assurance Performance Improvement programs. Director of Nursing or management experience in long-term care, restorative, or geriatric nursing. Ciena Healthcare is Michigan's largest provider of skilled nursing and rehabilitation care services.