clinical case manager salaries in boston, massachusetts

Randstad is working with a premier firm in Downtown Boston, MA to join their medical case review team. This role will join a team of highly tenured individuals in a new position due to growth and influx of work. This company highly values work/life balance, is a human first environment, and has a Monday-Friday 9AM-5PM schedule. This is a fully onsite position in Downtown Boston, MA, and is an excellent way for a driven, highly attention and detail oriented professional to build their career in a high growth position. The ideal candidate will have experience and education in a medical/healthcare setting, a Bachelor's Degree, and a desire to get into a dynamic legal organization. Qualifications: -Bachelor's degree in biology, health sciences, or related; pre-health concentration a plus -Highly intelligent, analytic, and detail-oriented -Driven by completing tasks and checklists -strong attention to detail and computer skills  salary: $55,000 - $60,000 per yearshift: Firstwork hours: 9 AM - 5 PMeducation: BachelorsResponsibilities-Extract Key Clinical Information: Utilize structured checklists to precisely identify and flag vital clinical data from essential medical records (e.g., pathology, delivery, and operative notes). -Facilitate Medical Review for Court: Help prepare the medical review sections of court documents by digitizing scanned records for search ability and creating comprehensive tables of contents for easy navigation by nurse investigators. -Inform Case Strategy: Conduct focused medical research to provide critical support for ongoing case development. -Protect Sensitive Data: Carefully review medical records to redact confidential content.SkillsLegalData CollectionElectronic Health Records (EHR)MEDICAL MALPRACTICEmedical records (1 year of experience is preferred)QualificationsYears of experience: 1 yearExperience level: Entry LevelRandstad 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: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).This posting is open for thirty (30) days. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

job summary: This role will sit within the I & I TA and will be responsible for reviewing and enforcing lab safety and data quality in research practice and documentation and ensure compliance with company GRP and research ethics standards.   location: Cambridge, Massachusetts job type: Contract salary: $48 - 51 per hour work hours: 9 to 5 education: Bachelors   responsibilities: Job Responsibilities Electronic Lab Notebooks (ELNs) - Company uses BenchlingAct as the TA representative at the global Digital Lab Notebook forum; attend monthly meetings and bring back any relevant updates to the LT and the TA. Request account creation and access to ELN for new hiresTrain new hires on the functionality and use of ELN for research documentationHelp troubleshoot ELN related issues either directly or by interfacing with the local ELN representative. Notebook audits - Spot check ELN entries on an ongoing basis to make sure they are compliant with the company Global Research Policy and research ethics standards.Coordinate with the Lab heads and senior researchers and set up quarterly notebook reviews within the TA.Working with the lab heads and senior researchers, conduct an annual ELN audit for the TA; generate a report of the results and communicate the outcomes to individuals as well as to the LT.Act as Lab Notebook Audit lead Support the team with training on lab tools e.g. BiosourceEnable teams to overcome supply challenges for novel reagentsSpecific Pharmacology reports (SPRs) Lead project teams through the SPR processAct as an expert user of Veeva Vault and train scientists for report writingRigorously evaluate internal study reports and manuscripts for data consistency between the report and the cited ELN entries to support regulatory submissions.Coordinate with the biostatistics representative to verify data consistency in the statistical analysis (if any).Coordinate with dossier management group and biology leads to ensure study report conforms with the prescribed formatting requirements. Support with the audit and maintenance of equipment, instruments, and other laboratory systems to ensure compliance with corporate policies and regulatory requirements.Record, track, and notify supervisor/ LT of potential quality issues.Health and Safety audits and corresponding corrective actions - Waste Accumulation Area weekly inspectionLabels on all containersFlammable/acid/base cabinet volume checksLab spot checks for expired reagents/materialsAssist with any additional job responsibilities or tasks based on business or departmental needs, as assigned.   qualifications: Required Qualifications Bachelor's Degree plus minimum 5 years of immunology research experience in an academic or biopharmaceutical setting OR Master's Degree plus minimum 2 years of immunology research experience in an academic or biopharmaceutical setting OR PhD plus minimum 2 years of immunology research experience in a biopharmaceutical setting.Experience working to GLP standardsExtensive experience writing research reports for IND (Investigational new drug) filingsAbility to work independently or with minimal supervision and effectively within timelines and collaborate in a highly matrixed global environment.Possesses strong communication skills, an exceptional work ethic and a willingness to spend time mentoring others. Preferred Qualifications: Relevant immunology research experience in an academic or biopharmaceutical setting. #LI-AM1   skills: Immunology, Electronic Laboratory Notebook (ELN), Good Laboratory Practices (GLP), Investigational New Drug (IND) 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: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

job summary: Company is currently seeking an Analytical Chemist in our Pivotal Attribute Sciences Department in Cambridge, MA. This team plays a crucial role in pivotal phase analytical support, including product development support, testing of drug substances and drug products. The role will work closely with a team of analysts and scientists responsible for the technical aspects of developing analytical tools to gain understanding of key quality attributes in product and process for late phase synthetic small molecule, synthetic peptide and/or antibody peptide conjugates. The Scientist will integrate and optimally utilize platform and in-depth product attribute knowledge to advance Company products and ensure success through pivotal clinical phases to marketing authorization application.   location: Cambridge, Massachusetts job type: Contract salary: $35.00 - 42.36 per hour work hours: 9 to 5 education: Masters   responsibilities: Regularly perform and adequately document routine maintenance of the HPLC instrument.Ensure consumables and supplies are properly maintained and readily availableHand-on experience in sample preparation and analysis of synthetic in-process samples, lot release samples, and drug product formulations using primarily chromatographic and spectroscopic techniques.Organize and document analytical data under Good Documentation Practice using electronic laboratory notebook system.Perform all duties in accordance with established quality protocols and standard operating procedures (SOPs)Provide general laboratory support and other responsibilities as assigned by the Supervisor.  qualifications: Master's degree in Analytical Chemistry, Organic Chemistry, Physical, Pharmaceutical, Life Sciences or EngineeringHands on experience in chromatographic techniques such as: CEX, SEC and RPLCExperience in synthetic peptide and/or peptide antibody conjugates including theoretical knowledge, research, and hands-on experience to support process development/scale up activities and formulation development.Experience with operation, maintenance, and troubleshooting of laboratory equipment and instrumentation, especially chromatographic (e.g. liquid chromatography) and spectroscopic instruments (e.g. mass spectrometry).Experience in laboratory settings within the pharmaceutical or biotech industryTechnical aptitude for identification, development, and implementation of novel analytical technologies #LI-HK1   skills: Chemistry, Chromatography, High Pressure Liquid Chromatography (HPLC), Liquid Chromatography (LC), Good Laboratory Practices (GLP) 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: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.