Pharmaceutical Jobs - Remote Work From Home & Flexible
I'd accomplished everything I wanted to in my last position and there was no chance of advancement. I also wanted to change to a career where I was helping others and hopefully increase my salary. Being able to work from home is a big plus. Being a single dad, it's nice not to commute to work, and it's easier to work additional hours when needed. I found FlexJobs' customizable search filters most effective in mysearch.
David B. from Kansas City, MO United States —Hired at Included Health as Engineering Manager, Infrastructure
We all tend to second-guess our abilities, but FlexJobs boosted my self-esteem. I've been a nurse for over 15 years and had been in search of a more flexible way to serve patients. I dabbled in travel and per diem nursing, but neither of those options truly gave me the flexibility I longed for, so I became a FlexJobs subscriber. Working remotely will aid me in sticking to a daily routine, will improve my overall health and well-being, and will prevent me from eating out everyday.
Art M. from Montgomery, AL United States —Hired at Ontrak, Inc. as Care Coach
I applied to over 130 jobs online (on other sites) and had given up trying. I honestly had no success despite having what I considered related experience, an accredited course, and a national certification exam. I only applied to approximately 10 to 12 jobs on FlexJobs. It is the best resource for flexible work. I've never been happier with mycareer!
Jean B. from Jefferson Township, PA United States —Hired at Ciox Health as Coding Specialist
Welcome to remote, part-time, freelance, and flexible Pharmaceutical jobs!Pharmaceutical jobs are plentiful as the medical and healthcare industries continue to demand professionals who understand medicine and drug formulations to help patients overcome diseases and ailments. Pharmaceutical jobs range from clinical...More
Welcome to remote, part-time, freelance, and flexible Pharmaceutical jobs!Pharmaceutical jobs are plentiful as the medical and healthcare industries continue to demand professionals who understand medicine and drug formulations to help patients overcome diseases and ailments. Pharmaceutical jobs range from clinical trial associates to highly trained Pharmacist roles. There are also many remote jobs in Pharmaceutical sales and support that offer flexibility and advancement. If you are interested in the role of medication and new advancements in life-saving drugs, then a career in the Pharmaceutical industry might be a good fit for you.
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New!TodayProofread prescription drug labeling, packaging and submission documents for US & International markets -primarily in English. Spanish, or other international market proofreading capabilities will be an advantage. Review documents for accuracy, clarity...
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New!YesterdayExceed quarterly and annual bookings goals. Build sales pipeline of benefit brokers/consultants and employers under 20,000 lives.Strategically manage the sales process. Coordinate internal resources to further the sales efforts. Take part in meetings.
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FeaturedNew!2 days agoAs a Database Analyst, you will be responsible for using Microsoft Access, SAS and related applications (e.g. Geo Access) to increase efficiency and accuracy in the daily reporting. This is needed to support retail network accessibility and related...
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New!2 days agoProvides critical support in developing global regulatory strategy, planning and execution of global investigational and marketed prescription drug submissions and manages lifecycle regulatory activities in alignment with the Global Regulatory Lead (GRL).
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New!2 days agoResponsible for providing business operations support focused on patient access to client's specified products through interaction with the client's field sales team and customers related to business operations within a specific site of care.
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New!2 days agoCollaborate with corporate and business segment leadership in identifying and evaluating acquisition targets. Lead proactive originations of prioritized acquisition targets with variety of stakeholders including but not limited to founders, PE sponsors...
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New!2 days agoMonitors and analyzes proposed legislation and regulation to determine the effects on the industry; helps determine the most appropriate position for company; communicates those positions to federal and state teams as well as the relevant business...
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New!2 days agoDrug Safety Manager is part of the Project Delivery organization and is responsible for management in Drug Safety/Vigilance and will work according to company policies, SOPs, and regulatory requirements. Bachelor's degree and 10 years of experience.
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New!2 days agoLeads or contributes to cross functional teams: Labeling Committees, Labeling Teams, and provide direction and support to Product Review Council teams, Legal and other groups, as needed. Develop and maintain Target Product Label, Company Core Data...
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New!2 days agoLeads and manages all contract negotiations with assigned Pharma Manufacture partners. Develops and cultivates client relationships; prepares presentations and proposals in support of new business development. Requires a minimum of seven to ten...
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New!2 days agoConduct onboarding call to gather demographic information and assess patient and caregiver needs. Make decisions based on patient feedback and advises on appropriate resources available. Research options based on Needs Assessment and provide...
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New!2 days agoAssist sales representatives in scheduling in-services by gathering critical information. Register nurse consultants and completes setup of on-site account in-services. Handle the enrollment of new nurse consultants into MSL Program. Prepare, confirm...
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New!2 days agoThe FRS will manage daily activities that support appropriate patient access to our client's products in the provider offices and work as a liaison to other patient assistance and reimbursement support services offered by our clients. Our teams travel...
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FeaturedNew!2 days ago开发、执行和管理业务的分析ss and financial metrics as well as performance measures. Supports business leaders with analytical analysis to help drive decision-making. Financial forecasting and reporting. Develop and maintain...
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New!2 days agoLead discussions to develop copy for the company and brainstorms with staff to collect background information and manages copy deadlines by holding others accountable for their contributions. 7 years of relevant experience in editing and proofreading...
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New!3 days agoParticipates in regulatory compliance audits and inspections. Provide objective, independent assessment of site / business unit's quality, regulatory compliance and business risk to management. Assesses compliance risk and recommends corrective action.
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New!3 days agoSupport development and maintenance of standard PVA templates for use at global and local level. Collaborate with other Baxter businesses/functions and GPS to ensure that new/planned business/commercial relationships are notified to GPS and agreements...
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New!3 days agoLeads the development and annual update of the Medical Affairs Strategic Plan for a specific disease area(s) and/or products in oncology (including publication plan, scientific narrative, grants/CMS plan, IST plan, and product launch plans).
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FeaturedNew!3 days agoServe as Regulatory Affairs, Global Development Team member that proactively provides regulatory strategies and pathways contributing to the optimum development, registration, and approval of new products. Able to lead and/or support project teams in...
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FeaturedNew!3 days agoOversees study vendors and contractors to ensure clinical trials are executed with high quality and within timelines to meet budget parameters. Minimum of 5 years of relevant Clinical Operations experience including development of clinical plans...
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New!3 days agoDevelop and maintain a thorough understanding of the business needs of Biology and how IT can enable them. Understands how Biology fits with the larger organization and how data moves and is used. Translate business needs into requirements. Define...
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New!3 days agoDevelop and lead the global and US medical affairs strategy for ARV-471. Serve as Core member on the Global Asset Teams and lead the Medical Sub-team. Provide Medical Affairs representation on Publication Planning Committee. Participate in data...
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New!4 days agoAnalyze manufacturer contract terms to ensure compatibility with rebate technology. Perform contract set-up support as required for each rebate period. Assist with the coordination, analysis and validation of rebate reports and distribution of...
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New!4 days agoPerforms review of medication lists to understand and eliminate barriers to medication therapy while serving as the member's Pharmacy Navigator in order to achieve the following: Proper Medication Adherence. Minimize any gaps in therapy. Prevention of...
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FeaturedNew!4 days ago在这个角色你会帮助准确地阅读, interpreting and entering prescriptions into the computer system , including the calculation of doses, assignment of directions and accepting proper insurance payment in a timely fashion. You will...
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New!5 days ago监督第三方分析方法的发展s, method validation, and investigations for out-of-specification, out-of-trend, and/or abnormal results. Provide technical review of various reports and raw data packages, utilizing a solid familiarity...
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FeaturedNew!5 days agoProvide Regulatory Documentation Support to Global Regulatory Affairs team members for Product Registrations, Renewals, Launches, etc. Provide support and needed information to all global regions on all US products across the product portfolio so that...
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New!6 days ago实现FHI临床表现,RFP的一代& sales targets. Actively prospect & generate new sales & business opportunities within assigned customer territory. Cultivate strong, long-term relationships with customers & develop in-depth knowledge.
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New!6 days agoLead supplier qualifications and contracts for all critical suppliers. Lead supplier audits in assessing materials/capacity/production capabilities and overall business issues. Manage key suppliers to strengthen relationship while ensuring continuity...
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New!6 days agoReview and approval of master batch records; product and material specifications; certificates of analysis; stability protocols and reports; validation protocols and reports; and other GMP-related documentation as developed I generated by the CDMOs.
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New!6 days agoCommunicate and negotiate directly with co-developers/co-marketers/partners (e.g. distribution partners) and patient support program (PSP) / market research program (MRP) vendors (External Parties) related to development, implementation and maintenance...
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New!6 days agoBuild targeted digital marketing plans for market segments to support education and adoption. Oversee media, digital, and other agency partners. Review KPI reports. Observe and perfect digital and consumer marketing...
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New!6 days agoAs a strategic problem solver, this individual must have strong project management experience, the ability to identify needs, streamline processes and meet deliverables. This role will help support and understand current operations and redefine...
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1 week agoThe associate Director provides comprehensive project management support for one or more of our development teams, driving execution of the strategy, development, and maintenance of program timelines, and leads gap assessment and problem solving...
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1 week agoIdentify and foster new and existing strategically aligned relationships with key Global research sites and build support strategies to ensure success with the overall conduct and recruitment of clinical trials for early and late-stage assets in the...
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1 week agoGMA Publications Manager will help develop, deliver, and drive the execution of internal and external scientific communication strategy and related tactics including global publications (e.g., abstracts, posters, manuscripts) and scientific materials.
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Featured1 week agoCreates patient recruitment strategy for clinical trials based on indication, protocol, client goals and recruitment history. Recommends specific marketing/advertising tactics and/or study site materials. Triages and tracks proposal requests.
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1 week agoManages all clinical operational and quality aspects of allocated studies, of low to moderate complexity, in compliance with ICH GCP. In accordance to project specific requirements, assumes Clinical Study Manager (CSM) responsibilities on small and...
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1 week agoAct as US/EU local safety office and FDA/EMA point of contact for safety reporting. Submission of all individual case safety reports to FDA/EMA, and interactions support with business partners (license partners) and vendors for all case intake and...
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1 week agoResponsible for the conceptualization, design, build and maintenance of the financial tools used within Business Operations in support of the budget development and reporting needs for our internal and external clients as well as other duties.
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8 days agoThe Consultant and or Senior Consultant (depending on experience), is part of an elite team of consultants to audit, analyze, and model information to provide insight to their clients on matters related to Gross Profit, Gross to Net, Fair Market Value...
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Featured8 days agoThe responsibilities of the Pharmacy Service Representative are to assist with and provide resolution to colleagues and customers with any and all escalated issues regarding pharmacy services, customer service and work flow concerns.
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Featured8 days agoDevelop processes to understand and drive management of rebate & margin impacts of formulary strategies, pharmaceutical manufacturer contract changes, public policy changes, & other internal initiatives or external market events. Assess pharmaceutical...
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Featured8 days agoPreparation for study initiation and submission of required regulatory documents such as CV's, Laboratory Certificates, FDA Forms, 1572's, Financial Disclosure Forms, Training certificates, Delegation of Authority Forms, IRB submission and approvals...
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9 days agoOn-site or remote / virtual auditing to support approval of new CROs; on-going qualification of existing CROs; or to investigate specific events involving GCP and GLP compliance ( for cause' audits). Review and follow-up on audit responses from these...
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9 days agoWe are looking for a full-time Client Services Triage Specialist. This role will work collaboratively with other Client Services Team members to achieve department goals and contribute to the overall success of the company. HS diploma w/ 2+ years of exp.
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9 days agoAuthor responses to health authority questions within the required timelines. Author precursor documents such as the Process Chemistry and Formulation Development summaries to be used as the basis for regulatory filings. Review and adjudicate comments...
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10 days agoDevelop and justify modeling and simulation strategies and tactical plans for drug development programs in all stages through approval. Document modeling plans and results in plans, memos and reports in accordance with Arvinas SOP and general...
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Featured10 days ago1年以上经验in healthcare environment, with experience working with medical insurance, benefits verification, medical billing, or a related field. You are a critical liaison between our patients, healthcare professionals and insurance carriers.
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Featured10 days agoAs a Benefits Verification Representative, you are a critical liaison between our patients, healthcare professionals and insurance carriers. You will verify insurance coverage in order to process patient prescription orders in a timely manner.
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