Communications Jobs - Remote Work From Home & Flexible
I am a semi-retired healthcare professional who is starting a home business. I was looking for something where I could work part-time at home. Thank you for the help and guidance, and I wish you
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Nicole C.
from
Green Bay, WI United States — Hired at The Center for Client Retention as Client Engagement Surveyor
After struggling to find relevant jobs (part-time and telecommute) through other sites, I came across FlexJobs. It was very easy to set up an account and search for jobs that met my requirements and skills. After applying for a handful of jobs, I was hired by a company within just a couple of weeks of signing up for this site. I highly recommend
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Dianna C.
from
Chanhassen, MN United States — Hired at Cactus Communications as Proofreader
I have already recommended your website to others. I will be back if needed again. What helped me in my search was creating multiple profiles outlining the different areas I was looking at, and taking the Skills Tests when I could. This also allowed me to perform searches based on those profiles. When searching, I would save listings to review more in-depth and would send in applications and resumes on those jobs that interested
me.
Kelly T.
from
Piqua, OH United States — Hired at Appen as Social Media Consultant
Welcome to remote, part-time, freelance, and flexible Communications jobs! Communications specialists are dynamic professionals who spend a majority of their time creating and delivering effective communications to others for their organizations. They may design printed or web based promotional materials, newsletters, or... More
Welcome to remote, part-time, freelance, and flexible Communications jobs! Communications specialists are dynamic professionals who spend a majority of their time creating and delivering effective communications to others for their organizations. They may design printed or web based promotional materials, newsletters, or other marketing materials or they may be asked to speak on behalf of their company at events or through media like television and radio. Communications specialists most often work as part of a team in conjunction with their PR and Marketing departments. Communications professionals may also be called Public Relation or Marketing Manager, Freelance Writer, Journalist, Line Editor or Advertising Coordinator. If you are seeking a remote job in Communications, then you will want to check out the jobs below that are available in contract, freelance, part-time and full-time opportunities.
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FeaturedNew! YesterdayWork directly with the study teams: in the development of clinical research documents including research protocols, informed consent documents, case report forms, study team worksheets and other documents; to guide the preparation of regulatory agency...
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New! YesterdaySupport the Quality Management System including SOPs, training and CAPA. Process and maintain documentation for controlled documents, as required. Develop and administer training for employees and/or consultants. Host client/sponsor audits and support...
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FeaturedNew! YesterdayPerform and coordinate all aspects of the clinical monitoring process. You shall also be qualified to conduct monitoring activities independently. Bachelor's degree in a life sciences related field or a Registered Nursing certification or equivalent...
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New! YesterdayManage the development of the regional product label by collaborating with the Labeling Working Group to define commercial objectives in the context of available and expected scientific data, regulatory guidance and precedent.
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FeaturedNew! 2 days agoIndependently performs analytical testing, method optimization/validation, and/or other specialty technologies studies OR method transfers for pharmaceutical and biopharmaceutical compounds in a variety of formulations and/or delivery systems.
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FeaturedNew! 2 days agoThe PL Is accountable for the overall delivery of the project (quality, time, cost) on behalf of the organization. Establishes and communicates customer expectations to the project team with minimal direction. Ensures that escalation pathways are...
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New! 2 days agoA Research Project Manager may also be assigned to oversee various operational and training aspects of the EPIC / OnCore application used by the Research Enterprise. The RPM will work closely and collaboratively with a variety of faculty and staff at...
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New! 2 days agoLeading or supporting scientific aspects of research activities in the following areas: research designs, methodologies, analytical techniques, data analyses, and reporting. Uses subject matter expertise in leading or supporting the development of...
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New! 3 days agoAssist team in the coordination of project-related activities. Assist investigators in determining patient eligibility for studies; ensure eligibility criteria are documented on all patients and only eligible patients are enrolled. Explain studies.
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New! 3 days agoConduct medical record reviews for a variety of cancer types with a focus on tracking the trajectory of patient care and outcomes after a cancer diagnosis. Collect and enter research data. Interview study participants remotely or in person. Recruit...
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FeaturedNew! 4 days agoAccording to the specific role, coordinates, oversees and completes functions on assigned trials activities detailed on the task matrix. Performs department, Internal, Country and Investigator file reviews as assigned and documents findings in system.
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New! 4 days agoOversight of patient safety, data integrity such as reviewing study source data, review and sign off on CRFs, and review data queries, etc. Study participant interaction will be minimal.Must be aware of and comply with applicable regulatory requirements.
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New! 4 days agoOversight of patient safety, data integrity including reviewing study source data, review and sign off on CRFs, and review data queries, etc. Study participant interaction will be minimal. Active U.S. MD or DO to practice in the State of New Jersey...
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New! 4 days agoServes as a financial member of the Project Team with the goal to contribute towards timely, efficient, and accurate preparation and tracking of site payments. Reviews the financial section of the Clinical Trial Agreement (CTA) in order to prepare...
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New! 5 days agoLead the execution of chromatography (e.g., affinity, ion-exchange, size-exclusion) and filtration (e.g., tangential flow filtration, normal flow filtration) studies. Design and execute laboratory studies to evaluate novel technologies to improve...
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New! 5 days agoAct as person in plant (PIP) for key unit operations during critical production campaigns. Provide subject matter expertise on drug product investigations that result in timely closure of deviations and ensure implementation of robust solutions.
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New! 5 days agoProvide technical leadership for cell/gene therapy manufacturing process validation, process changes and improvements, external tech transfer, deviation investigations, and change management. Interact extensively with contract manufacturing...
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New! 5 days agoProvide scientific input during protocol development, study design, oversight of study conduct, interpretation of study results through the final study report. Interface with a cross-functional team including Clinical Operations, Data Management...
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New! 5 days agoFunction in a lead role, meet with Vitalief's clinical research client stakeholders to assess their current clinical trials operational environment and understand what their business objectives are. Utilize business process improvement and change...
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1 week agoReview and interpret clinical research protocols and develop budgets to capture trial activity. Negotiate directly with industry sponsors to reach an agreement on budget and payment terms. 2-4 years of experience in clinical research or financial field...
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Featured8 days agoEducate internal stakeholders & external customers on disease states applicable to our biomarker portfolio particularly for prenatal screening & oncology. Interact as a consulting expert with customers to assist in the development of pathways/ protocols.
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Featured8 days agoEvaluate the regulatory environment and support the products for the site. Advise on the optimal regulatory strategies, submissions product changes, and approval pathways.Provide regulatory strategy leadership & expertise to enable an optimized approach.
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Featured8 days agoCompletes study and site management activities as defined in task matrix, and as applicable and directed for study assigned. Completes and documents study-specific training. Orients and trains on any company/study-specific systems. Review materials.
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8 days agoWrite and implement SAS macros and other utility tools. Independently designs and codes SAS programs for assigned project(s), consistently meeting objectives of the deliverables. Codes complex SAS programs to analyze and report clinical trial data.
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Featured9 days agoProvide medical consultation to team members and answer study related medical questions. Communicate clearly with associates and clients, maintaining and open line of communication to ensure all procedures are followed appropriately.
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9 days agoContributes to the development and/or review of study-related documentation, including but not limited to monitoring plan, risk management tool, eCRF, manuals, training materials, safety and regulatory documents, and clinical study report, etc.
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9 days agoA dynamic Quantitative Researcher to work in collaboration with our engineers, data scientists and quantitative traders to support our low liquidity market-making initiatives. An ideal candidate lives and breathes math and statistics, enjoys digging...
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9 days agoSupport sales with clinical and technical demos of software products. Provide clinical guidance to sales, internal stakeholders, and customers as it relates to software. Collaborate with customers, sales, and customer success to define, document, and...
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10 days agoGuide all aspects of design, including visual design, interaction design, user experience, user research, and brand identity. Collaborate with cross-functional teams to develop design strategies that align with business goals and user needs. Develop...
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Featured10 days agoThe Senior Data Analyst will be responsible for implementing a range of moderate to complex analyses in support of clinical non-interventional studies (NIS)using collected data, such as chart reviews & prospective studies. PhD with at least 3 yrs of exp.
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10 days agoThe Senior Investigator Grants Associate position is designed to provide grant administration processing and financial support to the Finance Team and applicable project teams. The position requires the candidate to be detail oriented, analytical...
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10 days agoServes as a financial member of the Project Team with the goal to contribute towards timely, efficient & accurate preparation and tracking of site payments. Reviews the financial section of the Clinical Trial Agreement (CTA) in order to prepare the ...
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11 days agoRepresent Development Operations on the Program Team (contribute to drug development strategy, planning, timing, cost projections) at the program level as well as the individual clinical study level. The Clinical Operations Lead is accountable to...
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Featured11 days agoParticipate in the design of complex multi-form CRFs and the resulting electronic databases. Lead the efforts for data cleaning, editing, and validation. Implement variable derivation, conduct statistical analyses for the types of studies described...
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Featured11 days agoServes as the primary contact and lead between the sponsor and the organization at the project level.Drives and owns the overall delivery of the cross-functional project (time, cost, quality).Establishes, communicates and manages customer expectations.
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Featured11 days agoServes as the primary contact and lead between the sponsor and the organization at the project level. On projects where the scope requires, ensures clear delineation in responsibilities and communication pathways for secondary project leads (such as...
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Featured11 days agoAccountable for the overall delivery of the project (quality, time, cost) on behalf of the organization. Establishes and communicates customer expectations to the project team with minimal direction. Ensures that escalation pathways are adhered to...
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11 days agoProvide leadership in identifying and implementing appropriate statistical methodologies for evaluating all types of CMC data. Bachelor's + 10 years/Master's +8 years/PhD + 2 years of experience in a technical discipline (biostatistics, engineering...
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Featured12 days agoWorking with Research Leaders for preclinical/clinical research activities and drive Evidence Generation Strategy. Develop study-related materials (e.g. protocol). Perform assigned sub-project tasks with cardiovascular group clinical staff.
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Featured12 days agoPossess and maintain knowledge of pertinent human subject protections regulations including Office for Human Research Protections OHRP), Food and Drug Administration FDAregulations, ICH guidelines, and any other applicable laws, regulations, policies...
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15 days agoMust be able to quickly resolve issues and convey those issues to and from delivery and management teams, whether pertaining to a contractual question or an editorial production issue.Support the expansion and revenue growth of the overall division.
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15 days agoReviews research study submissions prior to IRB review for completeness and compliance to regulatory requirements. Reviews and edits research study consent forms for completeness, readability and format. Ensures integrity and security of IRB data.
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15 days agoReview clinical documentation, coding and hospital or professional fee claim or charge information in accordance with the Prospective Reimbursement Analysis (PRA) to determine if the items and services provided to patients enrolled in clinical research...
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16 days agoWill work to embed transition within the organization, delivering capability for staff to understand and respond appropriately to transition-related issues.Evaluate current processes and make recommendations on how to integrate them into new processes.
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16 days agoContinuously assess project status, reassess and revise risks, oversee issue documentation and escalation, and ensure the project team and stakeholders remain informed of project status, risks, and issues throughout the project (including both periodic...
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Featured16 days agoThe Medical Writer collaborates with internal and sponsor team members to interpret, distill, and summarize complex data concepts. Other tasks include presentation of clinical messages in clinical study reports, summarization of preclinical and...
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Featured16 days agoMonitors investigator sites with a risk-based monitoring approach applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and...
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Featured16 days agoServes as a creator/contributor for signal detection and product safety scientist tasks which are ultra-high in complexity or which concern ultra-high complexity products, under supervision by a more experienced team member. Conducts quality review...
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17 days agoParticipate with principal investigator, postdocs and department administrators in the preparation of the administrative components of proposals within parameters of sponsored and non-sponsored research guidelines. Oversee and communicate submission...
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17 days agoPerform Lead Biostatistician role on medium complexity studies, providing statistical oversight and attending relevant project meetings. Perform project management activities for identified projects including resource planning, timelines and milestone...
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