Collecting information
Organizing data
This unique opportunity is at a prestigious facility looking to hire a traveling therapist. This exciting area offers many recreational activities. As a premier travel therapy company, Host Healthcare offers top pay, excellent benefits, and personalized service. The ideal candidate for this position will be dedicated to providing patients with the highest level of service. The ideal candidate will also be knowledgeable in Medicare, Medicaid, and private insurance, as well as the ability to complete relevant insurance documentations.
Other RN or LPN duties as assigned. Current PPD or Chest X-Ray. Competitive pay & weekly paychecks.. We offer private duty nursing, skilled nursing, physical rehabilitation, companion care, respite care and behavioral care for individuals with chronic and acute illnesses and disabilities. Our commitment to quality customer service, compassionate patient care, and filling critical healthcare needs makes us a trusted partner wherever care is needed.
Founded in 1997 and built upon 25+ years of dermatology-specific experience, we are the only full-service dermatology CRO that takes products from concept to approval.. The RAM will also assist in developing regulatory strategies for both internal and external Sponsored projects and act as liaison between FDA and the Sponsor.. Assisting or acting as the primary writer of regulatory content included as part of a regulatory submission or application.. Planning, compiling, publishing and submitting Regulatory documents for INDs and NDAs, including Amendments, Supplements, and Meeting materials to the FDA. Occasional support related to BLA, IDE, and PMA applications may be required.. Please note the candidate must be currently residing in San Diego, CA or willing to relocate.
Job Title: Professional Nursing Care Specialist. As a skilled nursing care specialist, you will be responsible for delivering high-quality patient care in a fast-paced healthcare environment.. The ideal candidate will possess excellent clinical judgment, strong communication skills, and the ability to work effectively in a team setting.. A minimum of one year of experience in a related nursing specialty is preferred.. Certifications such as ACLS, PALS, and TNCC are mandatory.
Specific responsibilities will include: being the clinical or program lead for the development of clinical research strategies, clinical development plans, and independent direction of Phase 1-4 clinical studies collaboratively within cross-functional project teams (including clinical operations, preclinical/clinical pharmacology, biometrics, regulatory, drug safety, CMC). Partners with Drug Safety Pharmacovigilance on adverse event reporting and safety monitoring committees as required. Contribute to publication and presentation of data through scientific communications externally.. MD or equivalent degree with accredited residency training and board certification in Neurology; subspecialization (Fellowship trained) preferred and 8+ years experience in clinical drug development (Phase 1-3) in a pharmaceutical/biotechnology company, including significant experience in senior leadership role.. Extensive knowledge of clinical drug development is mandatory, including knowledge of clinical development planning, US and global regulatory requirements and submission standards, study design, biostatistics, Good Clinical Practice (GCP), comfortable with oversight of internal and CRO resources in study conduct, data collection and analysis, report writing, and scientific presentation of data, across early and late development phases
( *in collaboration with AbbVie ). The role involves working with cross-functional teams (clinical project managers, pharmacology, biometrics, regulatory, drug safety) to create and execute development plans that will lead to product approvals.. The role includes providing expert medical advice to navigate complex drug development and working closely with Research and Preclinical Development to develop biomarkers for early clinical evaluation.. Deep knowledge of drug development, regulatory issues, and clinical research processes.. Strong knowledge of GCP, regulatory procedures, translational medicine, and biomarker evaluation.
Reproductive Partners San Diego is a leading Southern California fertility clinic, internationally and nationally recognized for our success in IVF in vitro fertilization, egg freezing and other fertility treatments for our patients.. The Financial Director is a key leadership role responsible for overseeing all aspects of Revenue Cycle Management (RCM) and financial operations within the organization.. Manage the practices accounting functions, including general ledger, accounts payable/receivable, and payroll.. Deep knowledge of medical billing, coding, insurance reimbursement, and healthcare compliance.. Technical Skills: Proficiency in RCM software, EHR systems, QuickBooks, and financial reporting tools.
LVN Position Under the supervision of the Registered Nurse Supervisor, the LVN will deliver the direct patient care services within the LVN scope of practice required of the nursing component of the LifePlan as well as provide all day center nursing functions and procedures for the assigned shift, to include the provision of nursing and personal care services (including and not limited to toileting, transfers, showers, dressing, grooming, and ADL's).. Monitors and assess patients in the PACE Day center and report any variances to normal to the RN and RN Supervisor for further assessment.. Remind all staff of and ensure compliance to all objectives of the Quality Assurance Program as well as safety, environmental and infection control standards.. Skilled nursing and/or Adult Day Center experience Vaccine administration and documentation experience Wound care experience Graduate of an accredited program of vocational nursing or equivalent.. Associates degree in Nursing or related field Current CA Licensed Vocational Nurse License Current Basic Life Support Healthcare Provider Course Certification Good oral and written communication.
Provides leadership by working cooperatively with ancillary nursing and other patient team personnel.. Maintains standards for professional nursing practice in the clinical setting.. Candidate must have reliable transportation for travel assignments.. Contract start date: Travel and housing provided.. All medical/occupational health compliance items must be completed within 5 days of offer acceptance.
As a Graduate Pharmacy Intern, you will leverage your academic knowledge from pharmacy school into real-world applications, gearing up for a Pharmacist role.. With guidance from your preceptor and District Leader, you will follow a comprehensive training roadmap within 120 days of graduation, aimed at expanding your understandings of store, district, and regional pharmacy operations.. This hands-on experience will enrich your insights into patient safety, error prevention, quality assurance drug utilization review (DUR), and pharmacy professional standards.. Ensure smooth pharmacy operations by adhering to workflow procedures for prescription fulfillment.. Must be a PharmD graduate of an accredited program before commencing the Post-Graduate Training Program at CVS Health.
Designed for retail clinics and private practices, our platform is currently undergoing FDA review and aims to revolutionize routine blood testing by making it more accessible, affordable, and actionable.. Truvian is seeking an experienced and hands-on Senior Regulatory Affairs Manager to lead and execute all aspects of the company’s global regulatory strategy.. Key Responsibilities Support the regulatory strategy for Truvian’s portfolio of IVD products, ensuring proactive planning and timely execution of submissions to FDA (510(k), CLIA Waiver), Health Canada, European Notified Bodies (CE Mark/IVDR), and other international agencies.. Required Qualifications Bachelor’s degree in Life Sciences, Engineering, or a related discipline required; advanced degree (MS, PhD, PharmD) strongly preferred.. Kombucha, cold brew, and healthy snacks are always on tap
We are seeking a dedicated Critical Care Clinical Pharmacist to provide expert pharmaceutical care to critically ill patients within a dynamic intensive care environment.. This role involves close collaboration with medical and hospital staff during patient care rounds to ensure optimal medication management and patient safety.. Support pharmacy operations as needed.. Education and Licenses Doctor of Pharmacy (PharmD) degree required.. Certifications Board Certified Pharmacotherapy Specialist (BCPS) preferred.
Balboa Nephrology is the largest kidney care practice in California and participates in a national Medicare program focused on value-based care.. We will help you grow in your leadership experiences while learning the new value-based care world.. From one small office, BNMG now has 24 clinical offices throughout San Diego, Imperial, Orange and Riverside counties.. In addition to office and hospital-based patient care, Balboa physicians manage the dialysis treatments of approximately 4,500 patients at 88 dialysis centers and conduct Nephrology based clinical research at 6 centers throughout Imperial and San Diego counties (California Institute of Renal Research).. Get notified about new Revenue Cycle Manager jobs in San Diego, CA.
San Diego Be a part of a global team that is inspired to make a difference in the lives of people living with rare disease.. We are seeking talented individuals who will thrive in our collaborative, diverse, fast-paced environment and share in our mission - to identify, develop and deliver life-changing therapies to people living with rare disease.. We stick by our values centered on patients, courage, community, and collaboration to pursue our vision of becoming a leading biopharmaceutical company dedicated to the delivery of innovation and hope to patients in the global rare disease community.. The Senior Regulatory Affairs Specialist is a highly motivated, organized and detail-oriented individual who will be responsible for supporting the Regulatory Project Lead on development of regulatory strategy, submissions to FDA and multiple countries (EU, APAC, Latin America) globally, including initial CTAs, INDs, and various amendments and maintenance of regulatory applications.. Proficient in Microsoft applications; experience with Veeva Vault EDMS and smartsheet a plus.
Job Description We are seeking a motivated Regulatory Affairs professional to join our team and help advance the clinical development of oncology products at ORIC. In this role, you will collaborate closely with colleagues across regulatory operations, quality, CMC, nonclinical and clinical functions to support high-quality, timely regulatory submissions.. Responsible for the creation, assembly, review, and archival of complex regulatory submissions which require interaction with internal and CRO teams to ensure optimal execution.. Collaborate cross-functionally with regulatory operations, quality, CMC, nonclinical, clinical teams.. Excellent writing and editorial skills, with the ability to develop high-quality clinical-regulatory documents (eg, investigator brochures, briefing documents, IND amendments, Fast Track/ODD designation requests).. Experience with regulatory information management system (Veeva RIM) is a plus.