- Merck & Co. (Rahway, NJ)
- …for clinical supplies . - Interacts with key partner organizations such as clinical development, regulatory , quality and other supply chain areas to address ... Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing...(GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full c ompany's Research… more
- Eisai, Inc (San Jose, CA)
- …will have the primary role of demand generation by conveying complex clinical information to customers and key stakeholders consistent with the FDA-approved ... demand generation within assigned geography by effectively conveying complex clinical information to customers and key stakeholders.Develop, maintain, and execute… more
- Eisai, Inc (Raleigh, NC)
- …a difference. If this is your profile, we want to hear from you. The QA Specialist plays a critical role in ensuring the quality and compliance of commercial and ... clinical products manufactured at the Eisai Raleigh facility. This...is responsible for executing core quality assurance functions, supporting regulatory inspections, and collaborating with internal and external stakeholders… more
- Merck & Co. (Omaha, NE)
- …time. -We are seeking a Growth and Improvement minded Associate Specialist , Logistics who can help drive our Strategic Operating Priorities.Strategic SummaryThe ... Associate Logistics Specialist will be responsible for export of raw materials...closely with freight forwarders, QA departments, USDA and other regulatory officers. Provide data to the Finance department so… more
- Aequor (Thousand Oaks, CA)
- …work alongside other innovative, driven professionals in this meaningful role. Role: Specialist Manufacturing, New Product Introduction Let's do this! At we strive ... introduction of new products into the manufacturing plant. This " Specialist Manufacturing" role will serve as a New Product...vital to the impact that ATO B20 with a clinical and commercial product mix has to the network.… more
- Merck & Co. (Rahway, NJ)
- …Experience with sterile GMP facility startup.Knowledge of Investigational drug regulatory requirements.Understanding of Clinical Supply Chain Operations.Current ... biologics, vaccine) Drug Product development and Good Manufacturing Practice (GMP) clinical supply manufacturing facility in Rahway, New Jersey.The Sterile Process… more
- Eisai, Inc (Phoenix, AZ)
- …customer business, disease state, product prescribing information, approved promotional clinical trials, patient access to medication, and regulatory /compliance ... profile, we want to hear from you. The Senior Oncology Sales Specialist is responsible for meeting/exceeding sales goals through promoting Oncology therapeutic… more
- Merck & Co. (Rahway, NJ)
- …Global Workspace and Enterprise Services (GWES) and our research laboratories, Global Clinical Development for Southeast and part of Northeast US. This position will ... Skills, Procurement, Procurement Management, Production Planning, Project Procurement Management, Regulatory Compliance, Risk Management, Stakeholder Engagement, Stakeholder Management, Stakeholder… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking QA Validation Specialist III as part of the Quality team based in Raritan, NJ. Role ... OverviewThe QA Validation Specialist role is an exempt level position with responsibilities...within a cell therapy manufacturing plant to support both clinical and commercial requirements in a sterile GMP environment.… more
- Vanderbilt Health (Nashville, TN)
- …Under the guidance and supervision of the Principal Investigator, the Research Nurse Specialist II (RNS II) is responsible for assuring that the integrity and ... quality of the clinical research trial is maintained and that the trial...shipping guidelines. Participates in periodic site visits from sponsor, regulatory authorities and others to review research, source documentation… more
- Johns Hopkins Healthcare (Baltimore, MD)
- …procedures and quality assurance programs including proficiency testing and regulatory compliance. Provides technical consultation services for JHMI laboratories, ... science. Work Experience: Work requires a minimum of five years of clinical experience to acquire knowledge and familiarity with laboratory policies and procedures.… more
- Maine Medical Center (Portland, ME)
- …6 months separation from employment. We are looking for an experienced and compassionate Clinical Nurse Specialist - Adult Medicine to join the team at ... experience, and experience in a leadership role. Knowledge of regulatory standards and best practices for clinical ...requires excellent problem solving, communication, and organizational skills. The Clinical Nurse Specialist will be a key… more
- Abbott (Greenville, NC)
- …Our 114,000 colleagues serve people in more than 160 countries. JOB DESCRIPTION: Clinical Specialist II About Abbott Abbott is a global healthcare leader, ... personnel. Remains current on developments in field(s) of expertise, regulatory requirements, and a good working knowledge of company...EP products. Requires a minimum of 6 months in Clinical Specialist position. Minimum of 2 years… more
- Associated Urological Specialist (Chicago Ridge, IL)
- …Paid time off Paid holidays Profit sharing Retirement plan GENERAL SUMMARY Clinical Research Coordinator, RN's are primarily responsible for study coordination and ... study implementation, data management and integrity, and compliance with regulatory requirements and reporting. Requirements ESSENTIAL JOB FUNCTION/COMPETENCIES Responsibilities… more
- JAG Physical Therapy (Belleville, NJ)
- …maximizing functional independence. Staff Physical Therapist examines patients using fundamental clinical knowledge, implements a treatment plan and executes plan of ... an EMR software is preferred *Excellent oral, written communication *Strong clinical decision-making skills *Excellent work ethic and dedication to patient success… more
- The Travelers Indemnity Company (Diamond Bar, CA)
- …current or future goals. Certified Case Manager (CCM), Certified Disability Management Specialist (CDMS), Clinical Research Counselor (CRC), or Certified Rehab ... Ideal Candidate Have? Disability case management experience preferred. Prior clinical experience preferred. Familiarity with URAC standards Analytical Thinking:… more
- AdventHealth (Orlando, FL)
- …healthcare with visionary leadership and world-class resources. **The role you'll contribute:** Clinical Regulatory Specialist - Emergency Department (CRSED) ... Offers supports to staff. + Prioritizes, compiles, and maintains regulatory data as required for system initiatives and action...a RN program + Two years of recent ED clinical nursing experience + Basic Life Support (BLS) certification… more
- University of Pennsylvania (Philadelphia, PA)
- …of health and wellness programs and resources, and much more. Posted Job Title Clinical Research Regulatory Specialist B (Abramson Cancer Center) Job Profile ... Title Clinical Research Regulatory Specialist B Job Description Summary The Abramson Cancer Center (ACC) of the University of Pennsylvania is a world leader… more
- University of Southern California (Los Angeles, CA)
- … SpecialistApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ Clinical -Research- Regulatory - Specialist ... to support principal investigators and quality assurance systems for the Clinical Investigations Support Office. Provides regulatory affairs support,… more
- Penn Medicine (Philadelphia, PA)
- …life's work? Penn Medicine is seeking a full-time, day shift, hybrid Ambulatory Care Clinical Pharmacy Specialist , Regulatory for the Hospital of the ... University of Pennsylvania (HUP). Summary: The Clinical Pharmacy Specialist , Regulatory (CPS-R) ensures pharmacy compliance related to regulatory and… more
