Warehouse Clerk Rentokil Initial plcWarehouse ClerkFranklin, MA$18–$25 / hourThis role is responsible for daily operations in the Finishing Center by helping maintain the warehouse, assisting with plant maintenance, loading and unloading foliage trucks, and preparing branch deliveries. By applying to this job, you agree to receive initial texts from systems used on behalf of Rentokil North America, Inc., possibly including Workday, Loop, and HireVue.
Accounting Clerk SDL Search PartnersAccounting ClerkWakefield, MassachusettsThis role is responsible for managing day-to-day accounts payable and accounts receivable functions, ensuring timely and accurate processing of financial transactions. This is a temporary role with a high probability of turning into a full-time role for the right person.
Clinical Study Manager Integrated Resources, IncClinical Study ManagerCambridge, MassachusettsFull timeProvides Clinical Operations input to other important study activities, including but not limited to: site identification and selection, enrollment models, clinical supply planning and drug supply, organization of investigator and vendor meetings, development of informed consents forms, planning and management of Trial Master File, development of monitoring plans, development of IxRS systems, development of EDC / Case Report Forms, review of data during the study, data cleaning and database lock, writing the Clinical Study Report. 11 identify risks to study and develop risk mitigation plans, including communication and collaboration with Clinical Program Manager and Associate Director, Clinical Operations to escalate risks and ensure rigorous risk mitigation planning.
Administrative Assistant 2 - Clinical Practice Lahey Hospital and Medical CenterAdministrative Assistant 2 - Clinical PracticeMA$21–$28.26 / hourCustomer Service: Ability to provide a high level of customer service to patients, visitors, staff and external customers in a professional, service-oriented, respectful manner using skills in active listening and problem solving. Team Work: Ability to work collaboratively in small teams to improve the operations of immediate work group by offering ideas, identifying issues, and respecting team members.
Clinical Trials Safety Data Manager Integrated Resources, IncClinical Trials Safety Data ManagerCambridge, MassachusettsContractorConduct partner oversight and performance management on contracted work (e.g., monitoring reports, quality evaluations, annual meetings) Senior Manager, Safety Data Collection, Clinical Trials.• Communicates on PV legislation and regulatory commitments across the organization and externally Senior Manager, Safety Data Collection, Clinical Trials.• Acts as subject matter expert on Pharmacovigilance (PV) operations of Pre and Post-Marketing Clinical Studies during audits / inspections Senior Manager, Safety Data Collection, Clinical Trials. Report metrics and KPIs for Clinical Trial safety report collection Senior Manager, Safety Data Collection, Clinical Trials.• Oversee and ensure study safety operational requirements are operationalized Senior Manager, Safety Data Collection, Clinical Trials.• Support the following Strategic Partner / vendor oversight activities, in conjunction with relevant functions (such as Global Clinical Operations) in relation to Clinical Trial safety report collection.•
Clinical Data Manager Integrated Resources, IncClinical Data ManagerCambridge, MassachusettsContractorReview study database design and derivations to ensure the database will meetReview study validations and/or edit checks to ensure the quality of the dataManage Analytical Sciences project plan, report on progress of Analytical Sciences deliverables, identify and resolve issues, coordinate activities with the project team and management for assigned compoundsAnticipate and communicate resource and quality issues that may impact deliverables or timelines for a program or group of studies. Represents DM function on major matters regarding policies, plans and objectives and industry meetings as well as serve as a role model and mentor and thought leader for DM.Actively mentors Data Managers and Senior Data Managers.
Clinical & Translational Research Unit Lab Technician I Boston Children's HospitalClinical & Translational Research Unit Lab Technician IBoston, MA$19.06–$27.64 / hourUnder direct supervision of the BCH Clinical & Translational Research Unit (CTRU) lab supervisor, the primary on-site lab technician lab handles, processes and manages specimens entering the CTRU lab from research participants throughout the institution. Completes assigned tasks such as assisting with monitoring and maintenance of lab equipment, lab-related inquiries, and Clinical Research Operations (CRO) Continuous Quality Improvement projects and lab sample tracking database.
Senior Manager, Clinical Study Quality Lead (Hybrid) Vertex PharmaceuticalsSenior Manager, Clinical Study Quality Lead (Hybrid)Boston, MassachusettsRemote$137,800–$206,800 / yearThe Senior Manager, Clinical Study Quality Lead provides study-level quality oversight for assigned clinical trials to help ensure they are conducted in compliance with Good Clinical Practice (GCP), applicable global regulations, study protocols, and Vertex procedures. This is an individual contributor role focused on GCP quality assurance oversight for clinical trials, including risk-based audit strategy, quality risk identification, issue escalation, CAPA support, compliance trend analysis, and inspection readiness.
NewSenior Manager, Clinical Study Quality Lead Vertex PharmaceuticalsSenior Manager, Clinical Study Quality LeadBoston, MassachusettsRemoteThe Senior Manager, Clinical Study Quality Lead provides study-level quality oversight for assigned clinical trials to help ensure they are conducted in compliance with Good Clinical Practice (GCP), applicable global regulations, study protocols, and Vertex procedures. This is an individual contributor role focused on GCP quality assurance oversight for clinical trials, including risk-based audit strategy, quality risk identification, issue escalation, CAPA support, compliance trend analysis, and inspection readiness.
Director Clinical Research Alnylam Pharmaceuticals IncDirector Clinical ResearchCambridge, MA$255,000–$345,000 / yearBoard Certification (or equivalent) or specialist training in cardiology Expertise in heart failure and/or amyloidosis is desirable 3+ years industry experience or equivalent clinical academic experience Sound scientific and clinical judgment Familiarity with concepts of clinical research and clinical trial design, including biostatistics, and regulatory agency organization, guidelines, and practices Ability to effectively present ideas and document complex medical/clinical concepts in both written and oral communication History of solving problems while exhibiting superior judgment and a balanced, realistic understanding of issues Outstanding leadership and collaboration skills working within a matrix environment Experience and knowledge of working with biotech/pharma partner(s) Thrives in highly entrepreneurial biotech environment and embraces Alnylam's culture of science, passion and urgency. Influence internal and external audiences in a high impact, highly visible fashion A highly driven, dynamic, engaged and accomplished physician-scientist with experience and insight will thrive in this role.
Senior Medical Director Clinical Research - Neurodegeneration Alnylam Pharmaceuticals IncSenior Medical Director Clinical Research - NeurodegenerationMABoard Certification (or equivalent) or specialist training is highly desirable; drug development experience in neurology (Huntington's Disease) would be a great advantage, but not essential 10+ years industry experience or equivalent clinical academic experience Sound scientific and clinical judgment Successful track record of leading Phase 2/3 clinical programs (preferably in Huntington's drug development), including major interactions with Health Authorities Familiarity with concepts of clinical research and clinical trial design, including biostatistics, regulatory agency organization, guidelines, and practices Ability to effectively present ideas and document complex medical/clinical concepts in both written and oral communication History of solving problems while exhibiting superior judgment and a balanced, realistic understanding of issues Outstanding leadership and collaboration skills working within a matrix environment. Collaborate closely with Preclinical, Regulatory Affairs, Medical Affairs and Commercial to ensure tight strategic integration of product development plans Be accountable via Clinical Research and Operations for all relevant timelines and deliverables Drive/supervise all major written deliverables (regulatory submissions, original articles, abstracts), and presentation materials Be responsible (as appropriate in line with SOPs) for final review and sign off with respect to all controlled documents including protocols, IBs, informed consent forms Influence internal and external audiences in a high impact, highly visible fashion MD with strong research background or MD PhD, with a track record of successful research support and peer review publications.
Registered Nurse (RN) - Cardiovascular Suite Clinical Practice Specialist, 36 hours/week, rotating shifts Lahey Hospital and Medical CenterRegistered Nurse (RN) - Cardiovascular Suite Clinical Practice Specialist, 36 hours/week, rotating shiftsBeverly, MA$71,491.50–$157,135.50 / yearActual compensation is determined based on several factors, that may include seniority, education, training, relevant experience, relevant certifications, geography of work location, job responsibilities, or other applicable factors permissible by law. Demonstrates strong interpersonal skills evidenced by the ability to communicate effectively and work collaboratively to promote teamwork among all care providers.
Sr. Medical Director Clinical Research- CVM Alnylam Pharmaceuticals IncSr. Medical Director Clinical Research- CVMCambridge, MA$259,300–$350,800 / yearMD or MD PhD, Board Certification (or equivalent) or specialist training in Nephrology is preferred 5+ years industry experience with early phase clinical program leadership experience in CVM or renal drug development, including leading trial design and execution and successful regulatory interactions Ability to develop state-of-the-art CDPs and to navigate through internal governance boards in securing strategic approval of CDPs as well as resource planning and assignment Experience in effectively leading x-EA global clinical team (or CDST equivalent), managing direct reports with strong mentorship, and exhibiting effective collaborations with other EAs to fulfill program goals and objectives Sound scientific and clinical judgment LI-JB1 #LI-Hybrid U.S. Pay Range $259,300.00 - $350,800.00 The pay range reflects the full-time base salary range we expect to pay for this role at the time of posting. Serve as early clinical research lead on ePT (Early Project Team) or chair of CDST (Clinical Development Sub-Team) depending on the stages of programs, with accountability for the Clinical Development Plan.
NewClinical Research Coordinator II Mass General BrighamClinical Research Coordinator IIBoston, MassachusettsFollowing established policies, procedures, and study protocols, provides assistance on clinical research studies, including recruiting, evaluating, and consenting patients for studies; collecting and organizing patient data; scheduling patients for study visits; performing clinical tests such as phlebotomy, EKGs, EEGs, etc. The Massachusetts General Hospital Department of Emergency Medicine's division of clinical research is seeking a highly motivated individual with a minimum of one year hands-on clinical research experience to assist with ongoing and future clinical research studies as Clinical Research Coordinator II.
Outpatient Clinical Dietitian- Part time (20hrs/WK) Boston Medical CenterOutpatient Clinical Dietitian- Part time (20hrs/WK)Boston, MA$25.48–$37.02 / hourThe Outpatient Dietitian plays a key role in the creation and management of complex dietary regimens and protocols within the department and plays an active role in developing nutrition based programming, and in the mentorship and education of peers, staff, and students demonstrating consistent high level of competency. POSITION SUMMARY: The Outpatient Dietitian assesses, develops, and coordinates medical nutrition therapy and education activities for patients with complex nutritional needs in the treatment of chronic disease including but not limited to weight management, diabetes, heart disease, allergies, GI disorders, and malnutrition.
IO&E Clinical Specialist - Part-Time- Boston Boston Scientific CorpIO&E Clinical Specialist - Part-Time- BostonBoston, MA$45,000–$60,000 / yearThe anticipated annualized base amount or range for this full time position will be $45,000 to $60,000, plus variable compensation governed by the Sales Incentive Compensation Plan (which includes certain annual non-discretionary incentives based on predetermined objectives) as well as the value of core and optional benefits offered at BSC, which can be reviewed at www.bscbenefitsconnect.com. Code § 2.2-4312 (2000), Boston Scientific is providing notification that the unlawful manufacture, sale, distribution, dispensation, possession, or use of a controlled substance or marijuana is prohibited in the workplace and that violations will result in disciplinary action up to and including termination.
Senior Medical Director, Clinical Development- POVE Vertex PharmaceuticalsSenior Medical Director, Clinical Development- POVEBoston, Massachusetts$280,600–$420,800 / yearThe Senior Medical Director will define the clinical development strategy of povetacicept in primary membranous nephropathy, work with cross-functional multidisciplinary teams to define overall asset strategy as well as clinical trials strategy, design and execution, and may serve as the Medical Lead for clinical trials that will be conducted with these compounds. At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations.
Senior Clinical Trial Associate - Oncology Obsidian Therapeutics IncSenior Clinical Trial Associate - OncologyBedford, MA$108,000–$132,000 / yearAs a member of our Clinical Operations Team, you will be a vital part of a highly collaborative organization working to achieve Obsidian's vision by translating innovative science into medical breakthroughs for patients starting with our lead program OBX-115, a novel engineered tumor-infiltrating lymphocyte (TIL) therapy. You'll play a key role in driving the operational execution of complex clinical trials, supporting cross-functional coordination, vendor oversight, and ensuring high-quality, inspection-ready study delivery.
Pediatric Speech Language Pathologist Clinical Fellow (SLP-CF) Cortica - NeurodevelopmentalPediatric Speech Language Pathologist Clinical Fellow (SLP-CF)Burlington, MA$90,637–$112,082 / yearMultidisciplinary Collaboration: Work alongside neurologists, developmental pediatricians, nurse practitioners, ABA professionals, occupational therapists, physical therapists, and music therapists in a truly integrated care model that reflects the latest research and promotes better outcomes. Low Billable Target, High-Quality Care: With a manageable caseload (22.75 billable hours/week) , you'll have the time and flexibility to deliver meaningful, outcome-driven therapy rather than focusing on quantity over quality.
Clinical Laboratory Assistant II HCA HealthcareClinical Laboratory Assistant IIManchester, NHCollect venous and capillary blood samples for Transfusion Service, Hematology, Chemistry, and Microbiology, from inpatients and outpatients of the patient population served by the hospital upon request or as assigned, performing accurate patient identification, requisition verification, specimen labeling, specimen handling and disposal of contaminated waste and sharps. Performs a variety of clinical support duties involved with the phlebotomy collection, accessioning, identification, and processing of clinical specimens and the performance, reporting and documentation of waived and/or Point of Care Testing in the clinical laboratory areas, to include microbiology, serology, chemistry, hematology, urinalysis.