Pharmacist Salary at Biomarin BETA

Join us as a Pharmacy Tech – Make an Impact! Location: Greenbrae, CA 94904 Job Type: 13-Week Contract Shift: Rotating shift 8 hrs. Days and Nights Scheduled Hours: 40 Hours a Week. Weekly Compensation: $1460.00 – $1560.00 What will you do: Prepare and dispense medications accurately under the supervision of a pharmacist. Receive, verify, and process prescriptions and refill requests in the pharmacy system. Manage inventory by ordering, stocking, and organizing medications and supplies. Provide customer service by answering phone calls, assisting patients, and providing information on medications. Maintain accurate patient records, labeling medications, and handled insurance claims. What You’ll Need: Current California Pharmacy Tech license. Must have one year of Recent Experience Able to use Pyxis system and Narcotic handling Don’t miss this opportunity – Be a part of one the best health care facilities!! Pride Global offers eligible employee’s comprehensive healthcare coverage (medica

Lead in Coordinating and site management of all aspects of clinical study from start-up to closeout, Supervise in- field clinicians, phlebotomist, pharmacists, nurse, technician, administrative staff, and data team. Set up study site for coordination, operation and management. Performs all aspects of the start-up process to include the development and approval of study specific documents, study schedules, and clinical planning. Clinical Operations Look into business development opportunities Conducted patient assessments and data collection according to study protocols Site management tasks Study coordination tasks Patient recruitment tasks Project management Research Administration Staffing, Staff Management and Training Data Integrity Regulatory compliance for all studies including coordination, submissions, and maintenance of regulatory files Set up SFRI SMO satellite program development in the region, including business development for the satellite sites. Patient Recruitment/Patie

Lead in Coordinating and site management of all aspects of clinical study from start-up to closeout, Supervise in- field clinicians, phlebotomist, pharmacists, nurse, technician, administrative staff, and data team. Set up study site for coordination, operation and management. Performs all aspects of the start-up process to include the development and approval of study specific documents, study schedules, and clinical planning. Clinical Operations Look into business development opportunities Conducted patient assessments and data collection according to study protocols Site management tasks Study coordination tasks Patient recruitment tasks Project management Research Administration Staffing, Staff Management and Training Data Integrity Regulatory compliance for all studies including coordination, submissions, and maintenance of regulatory files Set up SFRI SMO satellite program development in the region, including business development for the satellite sites. Patient Recruitment/Patie

Lead in Coordinating and site management of all aspects of clinical study from start-up to closeout, Supervise in- field clinicians, phlebotomist, pharmacists, nurse, technician, administrative staff, and data team. Set up study site for coordination, operation and management. Performs all aspects of the start-up process to include the development and approval of study specific documents, study schedules, and clinical planning. Clinical Operations Look into business development opportunities Conducted patient assessments and data collection according to study protocols Site management tasks Study coordination tasks Patient recruitment tasks Project management Research Administration Staffing, Staff Management and Training Data Integrity Regulatory compliance for all studies including coordination, submissions, and maintenance of regulatory files Set up SFRI SMO satellite program development in the region, including business development for the satellite sites. Patient Recruitment/Patie

Lead in Coordinating and site management of all aspects of clinical study from start-up to closeout, Supervise in- field clinicians, phlebotomist, pharmacists, nurse, technician, administrative staff, and data team. Set up study site for coordination, operation and management. Performs all aspects of the start-up process to include the development and approval of study specific documents, study schedules, and clinical planning. Clinical Operations Look into business development opportunities Conducted patient assessments and data collection according to study protocols Site management tasks Study coordination tasks Patient recruitment tasks Project management Research Administration Staffing, Staff Management and Training Data Integrity Regulatory compliance for all studies including coordination, submissions, and maintenance of regulatory files Set up SFRI SMO satellite program development in the region, including business development for the satellite sites. Patient Recruitment/Patie

Lead in Coordinating and site management of all aspects of clinical study from start-up to closeout, Supervise in- field clinicians, phlebotomist, pharmacists, nurse, technician, administrative staff, and data team. Set up study site for coordination, operation and management. Performs all aspects of the start-up process to include the development and approval of study specific documents, study schedules, and clinical planning. Clinical Operations Look into business development opportunities Conducted patient assessments and data collection according to study protocols Site management tasks Study coordination tasks Patient recruitment tasks Project management Research Administration Staffing, Staff Management and Training Data Integrity Regulatory compliance for all studies including coordination, submissions, and maintenance of regulatory files Set up SFRI SMO satellite program development in the region, including business development for the satellite sites. Patient Recruitment/Patie

Lead in Coordinating and site management of all aspects of clinical study from start-up to closeout, Supervise in- field clinicians, phlebotomist, pharmacists, nurse, technician, administrative staff, and data team. Set up study site for coordination, operation and management. Performs all aspects of the start-up process to include the development and approval of study specific documents, study schedules, and clinical planning. Clinical Operations Look into business development opportunities Conducted patient assessments and data collection according to study protocols Site management tasks Study coordination tasks Patient recruitment tasks Project management Research Administration Staffing, Staff Management and Training Data Integrity Regulatory compliance for all studies including coordination, submissions, and maintenance of regulatory files Set up SFRI SMO satellite program development in the region, including business development for the satellite sites. Patient Recruitment/Patie

Nimble is a healthtech company on a mission to simplify access, understanding and management of healthcare. We are starting by building the largest, most loved pharmacy business in the world. We are a fast-growing, technology-first startup driven by perfecting the patient and pharmacist experience. Nimble fosters a culture of collaboration, open communication and deliberate action that allows us to face today’s most exciting challenges head-on and grow incredibly quickly. The Client Partner Associate is a crucial member of the Nimble team, supporting new and current pharmacy partners as the lead point of contact, post launch. As we continue to grow nationwide, you will increase client engagement with Nimble features and create new sales opportunities by aligning pharmacy goals with revenue-focused growth. The ideal candidate is a proactive communicator, a problem-solver, and a team player with a passion for customer satisfaction and building their career in a post-sales role! You will: