pharmacist salaries in boston, massachusetts

job summary: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. With a hefty goal of discovering medical breakthroughs to treat devastating neurological ailments, our partner is focused on furthering research and finding ways to improve our healthcare system. You can feel secure in the fact that you will be paving the way to life changing practices when you work for this well-known team!   location: Telecommute job type: Contract salary: $175.00 - 202.49 per hour work hours: 9 to 5 education: Doctorate   responsibilities: The Global Safety Contract Physician will support the safety team for assigned products and activities, and will have the medical safety expertise to perform obligatory safety functions with oversight from the product-specific Global Safety Officers. support for global pharmacovigilance of assigned products as needed, including the review and analysis of safety data from clinical studies, the post-marketing setting, and the scientific literatureassistance with signal assessmentsassistance with the preparation and review of aggregate reports, core documents, and labelling updates as requiredassistance with the preparation and review of regulatory filing dossiers and responses to regulatory authority requestsserving as a safety MD representative for assigned study management teams, including the review of clinical study documents and reportsproviding safety MD representation for publications team meetings and review of publications.  qualifications: MD required; subspeciality focus in neuroscience preferredMinimum 5+ years of experience in the pharmaceutical industry or clinical care setting; ideally with 3-5+ years of overall experience specific to pharmacovigilancePrior experience in clinical trials (academic and/or industry)Knowledge of pre- and post-marketing US and EU regulationsFlexibility; dependability; strong written and verbal communication skills; ability to work well within a cross-functional team  skills: Drug Safety 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: As the world's largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. With a hefty goal of discovering medical breakthroughs to treat devastating neurological ailments, our partner is focused on furthering research and finding ways to improve our healthcare system. You can feel secure in the fact that you will be paving the way to life changing practices when you work for this well-known team!   location: Telecommute job type: Contract salary: $175.00 - 202.49 per hour work hours: 9 to 5 education: Doctorate   responsibilities: The Global Safety Contract Physician will support the Biogen safety team for assigned products and activities, and will have the medical safety expertise to perform obligatory safety functions with oversight from the product-specific Global Safety Officers. support for global pharmacovigilance of assigned products as needed, including the review and analysis of safety data from clinical studies, the post-marketing setting, and the scientific literatureassistance with signal assessmentsassistance with the preparation and review of aggregate reports, core documents, and labelling updates as requiredassistance with the preparation and review of regulatory filing dossiers and responses to regulatory authority requestsserving as a safety MD representative for assigned study management teams, including the review of clinical study documents and reportsproviding safety MD representation for publications team meetings and review of publications.  qualifications: MD required; subspeciality focus in neuroscience preferredMinimum 5+ years of experience in the pharmaceutical industry or clinical care setting; ideally with 3-5+ years of overall experience specific to pharmacovigilancePrior experience in clinical trials (academic and/or industry)Knowledge of pre- and post-marketing US and EU regulationsFlexibility; dependability; strong written and verbal communication skills; ability to work well within a cross-functional team  skills: Drug Safety, SD (Signal Detection) 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: As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. With a hefty goal of discovering medical breakthroughs to treat devastating neurological ailments, our partner is focused on furthering research and finding ways to improve our healthcare system. You can feel secure in the fact that you will be paving the way to life changing practices when you work for this well-known team!   location: Telecommute job type: Contract salary: $90.00 - 117.69 per hour work hours: 9 to 5 education: Doctorate   responsibilities: Plans and directs all aspects of an organization's medical policies, standards, and programs. Responsible for strategic clinical relationships with physicians and interns. Ensures all clinical programs are in compliance with all applicable regulations. Researches and studies current medical publications and data on new treatments and practices to ensure high quality clinical service offerings. Advises non medical management on clinical and patient related matters and policies. Requires an advanced degree of in medicine. Manages a departmental function within a broader corporate function. Develops major goals to support broad functional objectives. Approves policies developed within various sub-functions and departments. Typically requires 8-15 years of managerial experience. The Clinical Trial Physician will play a key role in a large global phase 3 lupus outcome study. In addition to the responsibilities described below, the CTP will be specifically responsible for reviewing participants medical conditions for study entry requirement. The tasks and activities of the Clinical Trial Physician will be carried out in close collaboration with the study Clinical Lead. Providing medical leadership internally for the trial activities assigned, through a comprehensive understanding of the science, medicine, product environment and competitive landscape relating to a disease areaContributing to the core medical/scientific information required in all clinical documents of the respective trial (e.g. protocols, core informed consent forms, clinical study reports, safety related documents etc.) and assure production of high-quality documentsSupporting the Clinical lead by:Delivering medical oversight of the study (including safety, medical review of data during the trial, quality and performance of the trial)Answering to trial-related EC/IRB and HA questionsDelivering medical training to the study teams' members and staff and protocol-related training to study sites  qualifications: MD, RheumatologistAt least 2 years' experience in clinical research in a Pharmaceutical and/or Biotech company or equivalent in Academia within lupus therapeutic areaExperience in patient education is a plusGood knowledge of drug development and clinical trial process based on previous experienceGood knowledge of regulatory requirements/ICH guidelinesGood organizational and communication skills, able to work as part of a team and independentlyResults driven attitude and good sense of urgencyAble to anticipate and proactively address issues and demands, solution oriented and hands-onAnalytical thinking, data and detail orientedShares knowledge and expertise openlyExcellent written and spoken communication skills in English  skills: Phase iii, ICH Regulations 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.