- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... experience data (PED) evidence to support optimization of access & reimbursement, clinical practice, product development and registration. The Director serves as a… more
- Merck & Co. (St. Louis, MO)
- …(eg, grants) to appropriate company resources consistent with applicable policies- Review headquarters-directed education and training to maintain current knowledge ... and comprehension of dynamic scientific and clinical environment in the company's areas of interestScientific exchange...by site or organization, with Friday designated as a remote -working day, unless business critical tasks require an on-site… more
- Merck & Co. (North Wales, PA)
- …to support collaboration to further differentiate our portfolio.The Medical Consult and Review Physician provides clinical expertise and advice to internal ... Promotional Review Team, the Medical Consult and Review Physician is responsible for ensuring the clinical...by site or organization, with Friday designated as a remote -working day, unless business critical tasks require an on-site… more
- Merck & Co. (Rahway, NJ)
- …and prepares , analy ze s , and/or develops mitigation strategies for review with clinical partners and senior leaders.- - Responsible and accountable ... Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing...by site or organization, with Friday designated as a remote -working day, unless business critical tasks require an on-site… more
- Merck & Co. (Rahway, NJ)
- …chain deliverables and prepares , analyses , and/or develops mitigation strategies for review with clinical partners and senior leaders. Works directly in the ... Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing...by site or organization, with Friday designated as a remote -working day, unless business critical tasks require an on-site… more
- Merck & Co. (North Wales, PA)
- …This may include:Serving as the lead clinical scientist on the clinical trial team.Leading medical monitoring team in review and interpretation of ... SummaryThis position leads the scientific planning and execution of one or more clinical trials or significant aspects thereof. In this position, you will have the… more
- Merck & Co. (Rahway, NJ)
- …to ensure a thorough understanding of the science behind the medicine and review further unmet medical needs to support collaboration to further differentiate our ... have a medical contact within the company.Upon request from Global Clinical Trial Operations (GCTO), support Company-Sponsored Trials to enhance the understanding… more
- Merck & Co. (Rahway, NJ)
- …at governance for the Cardiovascular & Respiratory portfolio (discovery therapeutic area review , early and late-stage clinical governance), and fully supportive ... Area and strategy, bridging the continuum from Discovery Research through Late-Stage Clinical Development.- The AVP provides strategic oversight for the early … more
- Merck & Co. (Rahway, NJ)
- …opportunity is fast paced and contributes to the Pharmaceutical Sciences and Clinical Supplies (PSCS) deliverable which is the development of robust compositions, ... will preferably have experience with high concentration biologics to support clinical and commercial development. Maintaining a strong network internally and across… more
- Merck & Co. (Memphis, TN)
- Job DescriptionOur Sales team support our customers by providing clinical information about products, educational information, clinical training programs and ... impact of those options on the patient. Must understand impact and use of clinical trials in multiple tumor types/ therapies, both in impact on promoted products and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …is a key role responsible for producing scientifically accurate, high-quality clinical regulatory documents while adhering to regulatory guidelines. This position ... requires collaboration across various functions to meet aggressive timelines. Clinical regulatory documents include, but are not limited to, clinical study… more
- Merck & Co. (Rahway, NJ)
- …potential medical breakthroughs.Support statistical programming activities for Early Oncology clinical development projects. Review the quality and reliability of ... statistical analysis and high-quality data to support decision making in clinical trials.Responsible for the development and execution of statistical analysis and… more
- Merck & Co. (MA)
- …impact of those options on the patient. Must understand impact and use of clinical trials in multiple tumor types/therapies, both in impact on promoted products and ... channels of drug distribution, Oncology GPO's, wholesalers and specialty pharmacies. Review and evaluate patterns for products purchased and prescribed, outpatient… more
- Merck & Co. (Rahway, NJ)
- …stakeholders across organizations such as Regulatory CMC, formulation functions, and clinical functions to ensure timebound progression of portfolio, initiatives for ... driving the development of in vitro-in vivo relationships and preclinical-to- clinical translation in bioperformance of formulationsThe Director will report to… more
- Merck & Co. (Rahway, NJ)
- …nomenclature data into a centralized databasePerforming data integrity review activities, including proofreadingDeveloping rules to ensure data qualityContributing ... and vaccinesBroad understanding of drug discovery, development and research, clinical data coding and experience working within a regulated environmentAbility… more
- Merck & Co. (Rahway, NJ)
- …a Global Labeling Lead, you will guide cross-functional teams in the creation, review , and approval of Core and Local Labeling documents.You will be responsible for ... relevant pharmaceutical industry experience (eg, Medical Affairs, Regulatory Affairs, Clinical , Pharmacovigilance).Current Employees apply HERE Current Contingent Workers apply… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Identify opportunities for improvement within the customer campaigns and engagement. Review and interpret campaign/tactic data to inform adjustments on customer ... and preferences Physical RequirementsHybrid: 3 days in office, 2 days remote . Approximately 20-30% overnight travel. Qualifications Requires a Bachelor's degree;… more
- Magellan Health Services (Boise, ID)
- …supervision. Project management skills and demonstrated experience. General Job Information Title Quality Clinical Reviewer ( Remote - Must live in Idaho) ... MFT) or a provisional license. - 3+ years of clinical experience - Will substitute 5 or more years...experience - Will substitute 5 or more years of clinical experience along with an Associates degree and RN… more
- Walgreens (Deerfield, IL)
- **Job Description:** **Job Summary:** Walgreens RWE (Real World Evidence) Clinical Trials is seeking a remote Account Manager, RWE Clinical Trials with ... disability/veterans". \#LI-TO1 **Job ID:** 1506161BR **Title:** Account Manager, RWE Clinical Trials - Remote **Company Indicator:** Walgreens **Employment… more
- Walgreens (Deerfield, IL)
- …for clinical trial design, protocol development, and execution including review of new business proposals, clinical trial data, feasibility analysis, ... issues + Provides medical review of eCRFs and data analysis plan for clinical accuracy + Reviews safety fields at case freeze for reconciliation (if needed) +… more
