Planet Pharma Jobs & Careers - Remote Work From Home & Flexible
About Planet Pharma
(A Division ofPlanet Group)
Researched & Written by Adrianne Bibby on the FlexJobs Team
Planet Pharma, part of The Planet Group, is a privately-held, global staffing and recruiting agency dedicated to serving businesses in the clinical, scientific, and technology sectors. Based in Northbrook, Illinois, Planet Pharma has additional locations in the greater Chicago, Illinois, area, as well as in San Francisco, California; Baltimore, Maryland; Durham, North Carolina; and London, England, United Kingdom. All of Planet Pharma’s offices share the company’s values of innovation, entrepreneurship, expertise, and passion, and they're dedicated to connecting top talent with opportunities around the world. As an employer, Planet Pharma has supported flexible work in the past by posting part-time, freelance, temporary, alternative schedule, flexible schedule, hybrid, and 100% remote job opportunities in fields likemedical & health,project management,math & economics,operations, andwriting.
Founded in 2009 by a dedicated team of experienced professionals, Planet Pharma offers staffing expertise to pharmaceutical, biotechnology, and medical technology organizations. The company’s services include contract staffing, direct hiring, outsourced projects, permanent placement, contract-to-hire staffing, and managed services. Planet Pharma’s approach to outsourcing helps businesses manage development costs by focusing on scalability, flexibility, sustainability, expertise, and value. Employing flexible service delivery models and cutting-edge technology, Planet Pharma delivers solutions that are customized to the needs of each client. The company’s goal is to strengthen the employer-employee dynamic by connecting its customers with valuable talent and by building enduring relationships.
Visit Planet Pharma's websiteCompany Divisions
For Research: Past Remote and Flexible Jobs at Planet Pharma
We include these past jobs as a way for you to explore what kinds of remote and flexible jobs Planet Pharma has hired for in the past and might be likely to hire for again in the future.
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22天前Collaborate with brand managers, external agency partners, and vendors to successfully manage and execute print programs. Performs all planning, production and execution of multiple master schedules for marketing materials. Management of print partner...
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22天前Conduct proofreading, editing, document formatting, review comment integration, and document completion/approval activities. Previous PSUR writing experience or experience writing documents relevant to EU MDR. Knowledge of EU MDR. University degree...
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23 days agoCreate communications plans. Manage, develop and execute deliverables per the communication plans. Ensure consistent messaging and integrated approaches across therapeutic communication strategies. Identity opportunities to improve the communications...
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30+ days agoNegotiate budgets for clinical site contracts, ensuring adherence to company guidelines and parameters. Work with legal team to ensure contracts meet legal and regulatory requirements. Liaise with CROs to manage negotiations for site contracts.
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30+ days agoPrepares, tracks, maintains and reviews required labeling documents (e.g. physicians label, patient insert, carton, label, blister, tenders) using Text verification Tools, and additional software or process tools to maintain change history for all...
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30+ days agoSummary: A Project Manager is needed to ensure all global, regional and functional QMS documents are cloned and updated, as necessary, to support the go-live of the new Kidney Co. This role will facilitate compilation of a list of all documents that...
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30+ days ago评估临床试验协议(主服务greements, Work Orders, and Clinical Trial Agreements) and site budgets with US and ex-US institutions for tracking purposes. Establish Purchase Orders (PO) via Client Finance system. Track and report...
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30+ days agoProofread 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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30+ days agoEnsure customer satisfaction through high-quality, efficient and reliable laboratory services. Oversee personnel training, development, performance, and professional growth. Oversee interactions with customers (contracting, data transfer, logistics...
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30+ days 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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30+ days agoDrawing vector-based, 3D projections (in particular, orthographic and isometric) of hardware products. Creating exploded-view drawings. Drawing 2D diagrams and flow charts. Taking and manipulating screenshots (including text in screenshots).
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30+ days agoProvides support activities and assists with the workflow for specific tasks on document publishing requests between client and our service providers; works closely with both service providers and client teams to communicate priorities for document...
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30+ days agoCreate communications plans. Manage, develop and execute deliverables per the communication plans. Ensure consistent messaging and integrated approaches across therapeutic communication strategies. Identity opportunities to improve the communications...
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30+ days agoPerforms publishing/formatting checks on clinical documents. Manages publishing of stand-alone documents and Clinical Study Reports (CSRs). Performs completeness checks and archival of supporting documents provided for publishing requests. Document...
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30+ days agoWork with scientists, medical leads, biostatisticians and the clinical affairs team to plan write and edit clinical study protocols and CSRs for registrational studies. Work efficiently and accurately adhering to best practices and departmental...
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30+ days agoDistill highly technical information for internal and external users while adhering to internal standards. Conduct independent research and liaise with subject matter experts to ensure accurate interpretation of complex technical data, drawings,...
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30+ days agoSupport the Technical Writer in writing technical documentation for ophthalmic surgical products and software for internal or external audiences. Extract written content and illustrations from provided documents and input that same content into...
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30+ days agoWrite, edit, perform data verification, submit for review, and obtain approval for clinical and nonclinical regulatory documents including, but not limited to, clinical protocols, clinical study reports (CSRs), investigator's brochures, summary...
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30+ days agoResponsibilities may include the following and other duties may be assigned. Creates, develops, plans, writes and edits operational, instructional, maintenance or test procedures for paper, multimedia, webbased publications and user sites; may produce...
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30+ days agoGrants Coordinator will be accountable for grants & sponsorship management, tracking, reporting, contracting, and PR/PO development. Bachelor's degree required. At least 1 years relevant experience.
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30+ days agoLead development and submission of an IND application package and develop regulatory strategy within the Immunology space. You must have had extensive interactions with FDA divisions of Dermatology & Dentistry and/or Gastroenterology (preferably both)...
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30+ days agoThe Medical Outcomes Manager will act as the primary liaison for the division with national and regional payers. The position has functional responsibility for payer interactions, including presentation of health economic data and medical value...
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30+ days agoThis role will be responsible for managing the migration of CBO data from internal data sources into CBO-developed applications. BA/BS degree and advanced Microsoft Excel user, Database/Data Warehouse experience preferred. 65+ WPM typing. Remote work.
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30+ days agoResponsible for Vendor Management of early phase development to commercial Quality function to ensure appropriate and timely vendor qualification and maintenance. Maintains and manages risk-based model for management and quality oversight of GMP and...
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30+ days agoPerform duties associated with Centers for Medicare and Medicaid Services (CMS) Recovery Audit contractor (RAC) program and other government regulatory and enforcement agency audits for documentation and billing compliance. This includes data entry,...
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