clinical case manager salaries in boston, massachusetts

job summary: 6-month contract Clinical Scientist role, requiring an experienced individual with an MS or PhD to support a high-priority Phase 3 Epilepsy Program. The role demands a mix of hands-on data review and cleaning, site query management, and scientific troubleshooting to ensure regulatory documentation is complete and timelines are met, with overtime required.   location: Needham Heights, Massachusetts job type: Contract salary: $80 - 95 per hour work hours: 9 to 5 education: Doctorate   responsibilities: Directly assist the Sr. Medical Director with high-volume data review and cleaning for a critical Phase 3 Pivotal Epilepsy Study.Manage and resolve site/data queries and implement documentation to close regulatory readiness gaps.Perform scientific deep-dive analyses on safety and efficacy data (e.g., lab results, adverse events) to identify trends.Serve as the scientific liaison for day-to-day study flow, requiring heavy cross-functional interaction with Data Management, Regulatory, and Medical Writing teams.Review and contribute to regulatory documents and clinical narratives as part of the documentation oversight requirements.  qualifications: Required: MS or PhD in Life Sciences, Biomedical Sciences, Pharmacology, or a related scientific discipline.3+ years of direct industry experience in clinical research3+ years of data review and data cleaning experience3+ years of site query management experience Preferred: Neurology experienceIndependent work ability #LI-AB1   skills: Site Management, Clinical Development Strategy 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: Global Medical Affairs Lead, Oncology 6 Month Initial Contract The Global Medical Affairs Leader is responsible for owning and executing medical affairs strategy across the company's Oncology portfolio, including pre-launch, launch, and lifecycle management. This role is critical in shaping the global medical strategy, driving external scientific leadership, and leading evidence generation to support registration, market access, and adoption. This position will report to the Vice President, Head of Medical Affairs Oncology and serve as the global medical lead with final accountability for the integrated medical plan and external scientific engagement for assigned oncology programs. The successful candidate will partner closely with global regulatory, clinical, commercial, and external stakeholders to ensure alignment and execution across the program lifecycle   location: Cambridge, Massachusetts job type: Contract salary: $150 - 155 per hour work hours: 9 to 5 education: Doctorate   responsibilities: Own and lead the global medical strategy for the Oncology portfolio, including end-to-end oversight from early development through commercialization and lifecycle planning.Provide medical leadership in governance bodies and global decision-making forums, ensuring medical alignment across development, regulatory, and commercial functions.Lead the cross-functional Development Integrated Evidence Team to build and deliver a comprehensive data package to support global regulatory authorities, payers, and healthcare stakeholders.Direct the global medical matrix team, including Scientific Communications, Field Medical, and Patient Advocacy, with ownership of cross-functional deliverables and execution timelines.Lead global launch readiness and execution for assigned oncology assets, including evidence generation, field medical training, scientific messaging, and external stakeholder engagement.Engage with global, regional, and national external experts to shape the scientific narrative, support clinical best practices, and influence policy and reimbursement discussions.Represent the company as the medical lead in global regulatory and payer engagements, providing strategic input and medical leadership in formal interactions.Drive the development and execution of publication strategy, real-world evidence initiatives, and global medical education programs to support external knowledge transfer.Steward the medical affairs budget and resource allocation for assigned oncology programs, ensuring alignment with franchise and enterprise priorities.Contribute to broader oncology franchise strategy in partnership with the VP and cross-functional leads, acting as a key voice in shaping medical direction and investment.  qualifications: MD or non-US equivalent, PharmD, or PhD with extensive oncology medical affairs leadership experienceMinimum of 15 years of experience in Medical Affairs, with a strong track record in global roles.Demonstrated leadership of global launch planning and execution in oncology or immuno-oncology settings.Deep expertise in oncology therapeutic area requiredStrong strategic thinking and leadership skills in a global medical affairs role.Experience in regulatory, scientific communication, and external stakeholder engagement.Launch experience global and/or locally. Preferred melanoma and immunotherapy experienceStrong track record of KOL engagement, scientific communication, and external representationExperience navigating strategic external collaborations and cross-company governanceExpertise in cross-functional team leadership, including pharmacovigilance, biostatistics, clinical operations, and regulatory affairsStrategic and operational mindset with excellent project leadership capabilitiesComfort managing cross-functional deliverables and owning timelines and outputs at a program level.Exceptional communication skills with the ability to translate complex science into clear, impactful messagingAbility to thrive in a fast-paced environment, balancing strategic leadership with hands-on executionA desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative. #LI-AT1   skills: Oncology, Medical Leadership, Medical Strategy, Key Opinion Leader (KOL), Medical Launches, Global Scientific Affairs Coordination 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 Posting: Manufacturing Associate I (Night Shift) - Lexington We are seeking a highly motivated Manufacturing Associate I (MA 1) to join the MA Bio Ops team at our client's facility in Lexington, MA. This role offers an immediate start in a critical production environment. Compensation: $28.00 per hour Duration: 6-Month Contract with potential for extension Shift: Night Shift  (2-2-3) The Role You will perform routine cGMP manufacturing operations for the production of clinical and/or commercial products, operating production equipment according to SOPs. Qualifications Experience: Normally requires a High School Diploma and 0–2 years related industry experience, OR an Associate’s Degree in a Life Sciences/Engineering field. A Biotech Certificate is desired. Key Skills: Familiarity with current Good Manufacturing Practices. Ability to follow written instruction. Possess excellent communication and troubleshooting skills. Familiarity with aseptic technique is a plus. Physical and Work Requirements This position is considered “Essential Personnel” and may require weekend or holiday off-shift support as needed. Ability to stand up to 6 hours in a production suite. Ability to lift, pull, or push equipment requiring up to 25–50 lbs. of force. Ability to gown and gain entry to biotechnology/pharmaceutical manufacturing areas. salary: $22 - $29 per hourshift: Thirdwork hours: 6 PM - 6 AMeducation: High SchoolResponsibilities cGMP Operations (80%): Carry out cGMP manufacturing operations utilizing Standard Operating Procedures (SOPs), Batch Records, and Form Preps. Documentation & Data: Execute and perform requests for GMP documentation. Enter data in systems like the Laboratory Information Management System (LIMS), MODA, or other business systems. Equipment Support (10%): Manage equipment by performing scheduled cleaning and standardization. Assist in the assembly and disassembly of process equipment. Quality & Training: Complete required training on time and identify changes needed to documentation. Maintain training requirements and personal development plans. The essential functions of this role include:working weekendsSkillsGMPClean RoomQualificationsYears of experience: 2 yearsExperience level: ExperiencedRandstad 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.