nurse salaries in boston, massachusetts

Join a dynamic healthcare community committed to innovation, excellence, and inclusivity. Work alongside top professionals in medicine, engage in groundbreaking research, and impact countless lives. Benefit from a culture of continuous learning, growth, and support, regardless of your career stage. Be part of a mission-driven organization shaping the future of healthcare globally.salary: $24 - $26 per hourshift: Firstwork hours: 8 AM - 5 PMeducation: High SchoolResponsibilitiesHere’s what you’ll be doing:The Senior Administrative Assistant supports the Cardiac Arrhythmia Service and Electrophysiology Program within Cardiovascular Medicine, handling various tasks across clinical, operational, and educational realms with discretion and organization. Schedule conferences, meetings, and appointments; coordinate national and international travel; maintain EP Faculty's clinical commitments schedule.Maintain Section Chief’s calendar; alert of unresolved issues or appointment conflicts before meetings.Assist physicians with administrative tasks; act as liaison to referring physicians, research personnel, vendors, and clinical staff.Manage physician and patient educational materials; assemble data for new clinical initiatives; organize faculty meetings and patient appointments; monitor clinical reports and physician adherence; handle incoming calls and visitors; ensure certification and licensure enrollment. Here’s what you’ll have: High School Diploma required3+ years medical office or Senior Administrative Support experienceCompetency in MS Word, Excel, OutlookHealthcare experience is a must Here’s what you’ll get: Above market pay at $26.00Excellent BenefitsFriendly coworkers and team membersSupportive management invested in your success Skills Administrative Duties (3 years of experience is required) Qualifications Years of experience: 3 yearsExperience level: Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad.Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).Applications accepted on ongoing basis until filled.

job summary: This role is key to help the medical supervision of clinical studies by Clinical Research Directors (CRD) and to ensure scientific management of clinical studies to be performed by the Clinical & Sciences Operations Platform (CSO) and Development Units in R&D.The primary purpose of the Clinical Scientist's position is to assist/support the Clinical Research Director in the medical/scientific contribution for the clinical studies e.g: supporting operational activities pertaining to the abbreviated protocol/protocol/amended protocol development (such as contribution to writing of protocol and/or amendments, informed consent, committees charters development and other study ancillary documents), support in the validation and clinical case review of study data, review of study plans and draft study reports/publications for accuracy, search of medical/scientific information for study teams, literature review and analysis, assists in the preparation of the responses for investigators, study teams, ethics committees or regulatory authorities, help manage study committees.Scope includes all R&D clinical trials for Riliprubart in CIDP (chronic inflammatory demyelinating polyneuropathy), from scientific assessment of a clinical project to final deliverable. The applicant must be able to use digital reporting tool, convinced and willing to promote their use. The applicant must be a fast learner as the work needs can change and evolve over time based on project progress. The applicant must be familiar with all medical and operational aspects related to the conduct of late-stage clinical trials.Under the guidance of the CRD he/she collaborates with the Coding specialist, Biostatisticians, Data Managers, Global and Regional Study Managers, Feasibility Managers, Pharmacovigilance representative, Medical Writer (e.g. planning and review of narratives) on high quality medical review, as needed. He/she supports the CRD to ensure appropriate documentation and consistency of the data and investigations of safety cases with the Clinical Trial Team (Monitoring Teams) or Pharmacovigilance.To better serve the activity, and depending on his/her experience, a Clinical Scientist can be dedicated to a specific task with minimal supervision (e.g. answering questions of local teams, managing validation strategy etc...), following business needs.   location: Cambridge, Massachusetts job type: Contract salary: $85.00 - 88.26 per hour work hours: 9 to 5 education: Doctorate   responsibilities: Ensure scientific support for the conduct of Riliprubart study(ies) he/she is allocated to by securing the operationalization of the medical validation/review plan (reports and trackers)Contribute to definition of the centralized monitoring strategy in consistency with the planned statistical analysis and is involved some of the study data validation and review processes, support the CRD for the Clinical Case review (safety events reported to Pharmacovigilance or safety events of special interest)Contribute to preparation and/or review of any documents related to the studies and requiring a scientific background (submission portfolio, abbreviated protocol/protocol/amended protocol, patient written information, presentations/communication to internal or external partners, study plans, study reports, trial disclosure form). Participates with the Study Team and monitoring team training on medical informationSupport CRD in the preparation of medical answers to questions from Health Authorities, IRB/Ethics Committees, investigators, experts involved in the study/project as neededIs involved in the quality and update of study documents, CRF adequacy with protocols/protocol amendments and will help in the objective of rationalizing and documenting the data collection needs quantitatively and qualitativelyHelp for the preparation, organization, conduct and minutes of Study Committees (eg. IDMC), follow the contracts with business support as neededSupport CRD in organizing/leading Steering committees, Data Monitoring Committees, Adjudication Committee meetings as neededSupport to regulatory documents filing and archiving.Is assessing, providing cost elements related to the study support in collaboration with study team, including planning management as needed  qualifications: Required Knowledge and Skills: Understand data collection, data flow, data validation, including medical validation and review processes up to data analysisAble to develop good quality management practices, including guidelines, as regard to medical data review activities, using a data-driven and risk management approachDigital and data orientedScientific expertise or interest and ability to learn in the domain of assigned study/projectAbility to take responsibilities on medical activities or endorse CRD decisions on his/her behalfQuality focused, detail-oriented and well organizedAbility to handle multiple tasks and to prioritizeStrong communication skills (verbal and written)Ability to synthesize the information, good presentation skillsAbility to work autonomously and to efficiently provide status reportsAbility to anticipate and timely escalate issues and to define appropriate action plansTeam and results orientedStrong English skills (verbal and written if English is the second language) Required Education/Experience: MD, Ph.D., Pharm.D., or similar; Bachelor's degree considered for candidates with experience. Previous experience in Clinical Research and/or Drug Development (e.g., at least 5-10 years within pharma industry or CRO or other clinical trial sites). Must have: Minimum Ph.D. or Pharm DPrevious senior clinical experienceMinimum of 5 years of clinic experience, review data, operation, and clinic dataExperience with Quality, deviations, Protocols and consentsMust have experience in late-stage clinical trials, medical monitoring, and data reviewsPrevious experience with medical validations/ reviews/ adverse events Nice to Have: Previous experience in neurology, neuroscienceMedical writing experience (drafting consents or protocols)Medical safety experience is a plus  skills: Pharmacovigilance, Data Validation Plan, Clinical Data Management Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility). Applications accepted on ongoing basis until filled.

job summary: This role is key to help the medical supervision of clinical studies by Clinical Research Directors (CRD) and to ensure scientific management of clinical studies to be performed by the Clinical & Sciences Operations Platform (CSO) and Development Units in R&D.The primary purpose of the Clinical Scientist's position is to assist/support the Clinical Research Director in the medical/scientific contribution for the clinical studies e.g: supporting operational activities pertaining to the abbreviated protocol/protocol/amended protocol development (such as contribution to writing of protocol and/or amendments, informed consent, committees charters development and other study ancillary documents), support in the validation and clinical case review of study data, review of study plans and draft study reports/publications for accuracy, search of medical/scientific information for study teams, literature review and analysis, assists in the preparation of the responses for investigators, study teams, ethics committees or regulatory authorities, help manage study committees.Scope includes all R&D clinical trials for Riliprubart in CIDP (chronic inflammatory demyelinating polyneuropathy), from scientific assessment of a clinical project to final deliverable. The applicant must be able to use digital reporting tool, convinced and willing to promote their use. The applicant must be a fast learner as the work needs can change and evolve over time based on project progress. The applicant must be familiar with all medical and operational aspects related to the conduct of late-stage clinical trials.Under the guidance of the CRD he/she collaborates with the Coding specialist, Biostatisticians, Data Managers, Global and Regional Study Managers, Feasibility Managers, Pharmacovigilance representative, Medical Writer (e.g. planning and review of narratives) on high quality medical review, as needed. He/she supports the CRD to ensure appropriate documentation and consistency of the data and investigations of safety cases with the Clinical Trial Team (Monitoring Teams) or Pharmacovigilance.To better serve the activity, and depending on his/her experience, a Clinical Scientist can be dedicated to a specific task with minimal supervision (e.g. answering questions of local teams, managing validation strategy etc...), following business needs.   location: Cambridge, Massachusetts job type: Contract salary: $85.00 - 88.26 per hour work hours: 9 to 5 education: Doctorate   responsibilities: Ensure scientific support for the conduct of Riliprubart study(ies) he/she is allocated to by securing the operationalization of the medical validation/review plan (reports and trackers)Contribute to definition of the centralized monitoring strategy in consistency with the planned statistical analysis and is involved some of the study data validation and review processes, support the CRD for the Clinical Case review (safety events reported to Pharmacovigilance or safety events of special interest)Contribute to preparation and/or review of any documents related to the studies and requiring a scientific background (submission portfolio, abbreviated protocol/protocol/amended protocol, patient written information, presentations/communication to internal or external partners, study plans, study reports, trial disclosure form). Participates with the Study Team and monitoring team training on medical informationSupport CRD in the preparation of medical answers to questions from Health Authorities, IRB/Ethics Committees, investigators, experts involved in the study/project as neededIs involved in the quality and update of study documents, CRF adequacy with protocols/protocol amendments and will help in the objective of rationalizing and documenting the data collection needs quantitatively and qualitativelyHelp for the preparation, organization, conduct and minutes of Study Committees (eg. IDMC), follow the contracts with business support as neededSupport CRD in organizing/leading Steering committees, Data Monitoring Committees, Adjudication Committee meetings as neededSupport to regulatory documents filing and archiving.Is assessing, providing cost elements related to the study support in collaboration with study team, including planning management as needed  qualifications: Required Knowledge and Skills: Understand data collection, data flow, data validation, including medical validation and review processes up to data analysisAble to develop good quality management practices, including guidelines, as regard to medical data review activities, using a data-driven and risk management approachDigital and data orientedScientific expertise or interest and ability to learn in the domain of assigned study/projectAbility to take responsibilities on medical activities or endorse CRD decisions on his/her behalfQuality focused, detail-oriented and well organizedAbility to handle multiple tasks and to prioritizeStrong communication skills (verbal and written)Ability to synthesize the information, good presentation skillsAbility to work autonomously and to efficiently provide status reportsAbility to anticipate and timely escalate issues and to define appropriate action plansTeam and results orientedStrong English skills (verbal and written if English is the second language) Required Education/Experience: MD, Ph.D., Pharm.D., or similar; Bachelor's degree considered for candidates with experience. Previous experience in Clinical Research and/or Drug Development (e.g., at least 5-10 years within pharma industry or CRO or other clinical trial sites). Must have: Minimum Ph.D. or Pharm DPrevious senior clinical experienceMinimum of 5 years of clinic experience, review data, operation, and clinic dataExperience with Quality, deviations, Protocols and consentsMust have experience in late-stage clinical trials, medical monitoring, and data reviewsPrevious experience with medical validations/ reviews/ adverse events Nice to Have: Previous experience in neurology, neuroscienceMedical writing experience (drafting consents or protocols)Medical safety experience is a plus  skills: Pharmacovigilance, Data Validation Plan, Clinical Data Management Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility). Applications accepted on ongoing basis until filled.