- Merck & Co. (Orlando, FL)
- Job DescriptionThe Virology (HIV) Regional Medical Scientific Director is a credentialed (ie, MD, PhD, DNP, or PharmD) therapeutic and disease area expert who ... when requested, with external scientific leaders and investigators in the medical and scientific community. - Virology RMSDs provide Scientific Leaders (SLs)… more
- Merck & Co. (North Wales, PA)
- Job Description Role Summary: The Global Senior Director Medical Affairs (GDMA) is a subject matter expert in their area of responsibility (eg, defined tumor, asset, ... vaccine) and responsible for driving execution of the Global Medical and Scientific Affairs (GMSA) portion for their assigned...in collaboration with RDMAs, while also serving as a review panel member on TA specific MISP's to support… more
- Eisai, Inc (Nutley, NJ)
- At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai's human health care ... a difference. If this is your profile, we want to hear from you. The Medical Science Liaison (MSL) is a field-facing representative of US Medical Affairs with… more
- eviCore healthcare (Indianapolis, IN)
- Provides timely expert medical review for requests to evaluate the medical necessity of services that do not meet utilization review criteria while ... the United States.Reviews appeals for denied services related to current relevant medical experience or knowledge in accordance with appeal policies, if so… more
- Eisai, Inc (Nutley, NJ)
- At Eisai, satisfying unmet medical needs and increasing the benefits healthcare provides to patients, their families, and caregivers is Eisai's human health care ... your profile, we want to hear from you. The Medical Science Liaison (MSL or Sr. MSL) is a...members without a direct reporting relationship Research Support Facilitate review and follow up of submitted Investigator-Initiated Studies (IISs)… more
- Merck & Co. (North Wales, PA)
- …main focus will be on document production processes, including content authoring, review and finalization, and feed to the Submissions Assembly team. The Business ... on requirements and design topicsSupport functional areas in identification and review of process questions and issues related to submission content management,… more
- Merck & Co. (Rahway, NJ)
- …laboratory practices and procedures in a GMP environment including microbiology data review and quality procedures.This position is based at the Rahway, New Jersey ... Quality, Pipeline, and Operations.Supervise microbiology testing, data entry, data review , and author /approve analytical reports and data summaries.Conduct project… more
- Merck & Co. (Rahway, NJ)
- …laboratory practices and procedures in a GMP environment including microbiology data review and quality procedures. This position is based at the Rahway, New ... stakeholders and partners, including Quality, Pipeline, and Operations.Second scientist review microbiology experiments in line with GMP expectationsSupport internal… more
- Merck & Co. (Rahway, NJ)
- …laboratory practices and procedures in a GMP environment including microbiology data review and quality procedures. This position is based at the Rahway, New ... and Operations.Perform microbiology testing and studies, data entry, data review , and author analytical reports and data summaries.Conduct project management… more
- HealthCare Support (Houston, TX)
- …HealthCare Company in Remote Houston TX . Daily Responsibilities for Utilization Review RN: WIll need to use their OWN EQUIPMENT: 2 screens, will need a ... guidelines. Refers cases that do not meet criteria to Medical Director for review . 2. Assists in discharge planning especially Home Health Nursing requests… more
- Genmab (NJ)
- …'face' with our sites.Additionally, the Manager may also support on-site and/or remote trial oversight activities (within a region upon request). If regional-level ... and relevant stakeholders to obtain in-depth requirements to support efficient review of the conduct, quality and integrity of the data.Responsibilities/tasks:The… more
- Merck & Co. (Rahway, NJ)
- …and/or support batch processing readiness and execution activities. Prepare, review , and/or approve GMP Documentation as appropriate. Author/Approve Standard ... share and align on best practices. Author lessons learnt through after action review summaries or other reports to capture knowledge gained. Drive new technology… more
- Merck & Co. (Millsboro, DE)
- …of federal, state, and local biosafety regulations, and advise management accordingly. Review risk assessments for biological materials and laboratory operations to ... to enhance biosafety awareness and practices among laboratory personnel.Develop, review , and update biosafety policies and standard operating procedures (SOPs)… more
- Merck & Co. (Rahway, NJ)
- …organized manner following ALCOA principals and SOPs. - Author and review technical documents. Complete assigned work within established project timelines. Support ... days may vary by site or organization, with Friday designated as a remote -working day, unless business critical tasks require an on-site presence.This Hybrid work… more
- Merck & Co. (Rahway, NJ)
- …culture by reducing waste and constantly driving continuous improvement. Responsible to review and approve compliance documents, as per procedures or need.-Supply - ... days may vary by site or organization, with Friday designated as a remote -working day, unless business critical tasks require an on-site presence.This Hybrid work… more
- Merck & Co. (Rahway, NJ)
- …Support compliance audits, inspection activities, and investigation/CAPAs.-- Author and review technical documents. Complete assigned work within established project ... days may vary by site or organization, with Friday designated as a remote -working day, unless business critical tasks require an on-site presence.This Hybrid work… more
- Merck & Co. (Rahway, NJ)
- …research studies, in collaboration with scientific leaders, veterinary medical centers, corporate veterinary health systems, research organizations, database ... analysis plans, clinical study reports and manuscripts intended for peer- review . To ensure findings are communicated effectively at scientific conferences,… more
- Merck & Co. (Millsboro, DE)
- …IPT support for audits, inspections, validations and corrective actions.Author, review and approve SOPs, Quality Notifications and technical documentation; ... days may vary by site or organization, with Friday designated as a remote -working day, unless business critical tasks require an on-site presence.This Hybrid work… more
- Merck & Co. (Boston, MA)
- …to therapeutic area governance, functional area experts and development review committees.Contribute to assessment of internal and external opportunities identified ... days may vary by site or organization, with Friday designated as a remote -working day, unless business critical tasks require an on-site presence.This Hybrid work… more
- Merck & Co. (Rahway, NJ)
- …of worldwide regulatory submissions.This position involves interaction with Medical , Data Coordination, Statistical Programming, Research Laboratories scientists and ... agencies, or investigators.-10. Responsible for ensuring the accuracy of Statistical Review Aids submitted to regulatory agencies.11. Participates with management in… more
