📑 Senior Clinical Trial Management AssociateW2 ContractSalary Range: $145,600 - $156,000 per yearLocation: Redwood City, CA - Hybrid RoleJob Summary:As a Senior Clinical Trial Management Associate, you will be responsible for Contract Research Organization (CRO) oversight and execution of clinical studies. This role is an opportunity for an experienc ...
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📑 The Trial Manager creates and ensures the successful execution of the clinical data management strategy for assigned trials within a specific drug/vaccine program. Develops and manages project plans which span from protocol development through database lock. Collaborates with appropriate functional areas to align resources and ensure all aspects of ...
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📑 Salary: $120-139K Company Summary: Working with a precision IO biotechnology company to build out their clinical operations team and they are currently looking for a Sr. Clinical Research Associate (SCRA) on a hybrid capacity in their SF office. Their mission is to develop best-in-class immunotherapies to address unmet needs within the oncology and ...
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📑 Hybrid Position | Located in San Diego, CA This Director of Clinical Operations will play a pivotal role in leading and supervising all activities related to clinical operations, including the management and execution of clinical trials in accordance with Good Clinical Practices (GCP) as well as in compliance with various governing regulatory agenc ...
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📑 Associate Director/Senior Manager, Oncology BiostatisticsLocation: Hybrid SF or PAContact: Susan Devine - sdevine@penfieldsearch.comOur client is a clinical-stage biotech company with an established track record and a strong pipeline in Oncology and Rare Disease, looking for an experienced Biostatistician. This is a hands-on role that will utilize ...
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📑 Clinical Development, Senior Manager/Associate DirectorTHE COMPANY89bio is a clinical-stage biopharmaceutical company focused on the development and commercialization of innovative therapies for the treatment of liver and cardio-metabolic diseases. The company's lead product candidate, pegozafermin (BIO89-100), is a specifically engineered glycoPEG ...
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📑 Title: Senior Medical Director, Clinical DevelopmentDescription: The Senior Medical Director, Clinical Development is a vital contributor to clinical development programs, overseeing study-specific activities, collaborating with cross-functional teams, and supporting regulatory activities. Responsibilities include protocol design, data analysis, co ...
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📑 Contract Senior Manager Clinical Inspection Readiness, Hybrid 3 days onsite in Northern NJ/New York areas. $80-100 phr plus benefits, PTO. 12 months renewable **No 3rd parties** No Corp to Corp**Description: Top pharmaceutical company in the area is looking for a Contract Senior Manager Clinical Inspection Readiness candidate to lead clinical inspe ...
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📑 An exciting biotechnology company are growing out their clinical trial function and consequently, looking for a Director, Clinical Operations to join the team based out of Massachusetts.About the CompanyAt the forefront of groundbreaking clinical trials, this company is spearheading scientific discoveries in the fields of oncology, cardiology, and ...
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📑 Director of Clinical Trial Supply - Clinical Packaging & Labelling - High growth business with strong financial backingAre you a talented leader, looking for that role to develop site capabilities, personnel and make a difference in the development of a high growth Clinical Trial Supply business?You will join a CTS business who specialise in the He ...
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📑 Candidates must be located in the United StatesReporting to the Associate Director of Clinical Operations, the Clinical Trials Manager will be accountable for managing the clinical operation activities for clinical studies. This person will be key in driving the clinical studies day to day activities, ensuring on time delivery of main clinical mile ...
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📑 Are you a detail-oriented QA professional with a deep understanding of Good Clinical Practice (GCP) guidelines? If so, I want to hear from you! We are partnered with a breaking clinical biotech company seeking a highly motivated Senior QA Consultant to join their growing team.What you'll do:Conduct comprehensive reviews of clinical trial protocols, ...
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📑 Site Lead / General Manager - Secondary Clinical Packaging & Labelling - Hybrid role in NJAre you a talented leader, looking for that role to develop site capabilities, personnel and make a difference in the development of a high growth Clinical Trial Supply business? You will join a CTS business who specialise in the Healthcare Logistics, expandin ...
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📑 Our client is a biotechnology company dedicated to the discovery and development of next-generation cancer treatments. The company has had great success building a clinically differentiated pipeline of small molecules and biotherapeutics, including antibody-drug conjugates, to target an expanding range of tumor types using multiple modalities and m ...
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📑 In this newly created position, the Associate Director/Director, Clinical Sciences will report to our Executive Director, Clinical Sciences with primary responsibility to further advance progress of our expanding ophthalmology program. In addition to planning, implementing, and managing clinical research studies in collaboration with internal and e ...
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📑 Our client is an established, mid-sized pharma specializing in developing novel therapeutics in the area of Oncology. They are seeking a Senior Director of Biostatistics to provide statistical input and support for clinical trial design, conduct data analysis, and results interpretation. This role may also be responsible for managing junior biostat ...
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📑 Our innovative Oncology ADC Pre-IPO biotech client is seeking a Medical Director / Senior Medical Director with strong Oncology Clinical Development experience to cover development programs spanning phases I, II, III.Responsibilities:Providing clinical leadership; from early-stage clinical trial design for novel cancer drugs through to CoP stageWor ...
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📑 The Executive/Senior Medical Director, Clinical Development will play a vital role in shaping the scientific, clinical, and operational aspects of our client's clinical development programs, focusing on study and program-specific activities. This position will lead the design, planning, and implementation of study protocols for assigned investigati ...
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📑 Beacon Hill Life Sciences is actively recruiting for a Senior Manager of GCP Quality Assurance to work a contract assignment, part-time hours. Part-time, approximately 20 hours per weekDuration of assignment: 6 months with possibility of extensionFully remote is possible, preference though is hybrid (Location: Cambridge, MA)Pay Rate is based on exp ...
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📑 We are partnered with a prominent biopharmaceutical company based in the San Francisco area in search of a Medical Director or Senior Director.Requirements:MD (or equivalent outside the US) with a minimum of 5 years of experience in clinical drug development within the biotech/pharma industry.Preference for board certification in Gastroenterology, ...
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📑 Drug Safety Specialist - 12 Month FTC Location Marlow, UK Requisition ID 2256 # of openings 1 Apply Now ( Job Brief <br ...
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📑 BioPhase Solutions specializes in recruiting top talented professionals for Southern California's Life Sciences community. We are currently looking for an ONSITE Sr. Clinical Trial Manager to work for a leading San Diego area biotech company.*Must be local to San Diego, CA.Key Responsibilities:· Oversee the performance of CROs and third-party vend ...
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📑 Clinical Monitor (West Coast highly preferred)Background: Our client is a small medical device and aesthetics manufacture that focuses on breast reconstruction clinical studies. They have a long-term Post Marker clinical study that is currently ongoing, and they are looking for a field clinical monitor to come on and help with clinical monitoring. ...
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📑 Our client, a small oncology-focused biotech company is currently looking for an experienced Contract Senior Clinical Trial Manager to join their dedicated team and play an important role in advancing groundbreaking cancer therapies through phase I and II.About the position/Requirements:8-10 years of experience in clinical and drug developmentExten ...
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📑 Job DescriptionThe Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Evaluates and abstracts research data and ensures compliance with protocol and research objectives. Responsible for completing case report forms, entering c ...
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📑 Clinical Business Operations, Associate Director/DirectorTHE COMPANY89bio is a clinical-stage biopharmaceutical company focused on the development and commercialization of innovative therapies for the treatment of liver and cardio-metabolic diseases. The company's lead product candidate, pegozafermin (BIO89-100), is a specifically engineered glycoP ...
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📑 Company overview:Nulixir, a nano-biotechnology start-up, is a VC-backed business-to-business (B2B) company that develops, manufactures, and licenses intellectual property (IP) for smart nanocarriers, called nanovesicles, which optimize the performance of functional ingredients in food & beverage products. Nulixir, as the Function HouseTM, is revolu ...
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📑 THE COMPANY89bio is a clinical-stage biopharmaceutical company focused on the development and commercialization of innovative therapies for the treatment of liver and cardio-metabolic diseases. The company's lead product candidate, pegozafermin (BIO89-100), is a specifically engineered glycoPEGylated analog of FGF21. Pegozafermin is being developed ...
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📑 About this position:The Clinical Trial Manager (CTM) position will provide support and/or leadership for one or more global cross-functional clinical studies (includes First-in-Human, proof-of-concept, dose-ranging, special populations Phase II trials). Experience working in a fast-paced, highly dynamic biotech environment is desirable. The CTM is ...
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📑 Company Description Andrade Gonzalez LLP is a DTLA boutique litigation firm. We use creativity, flexibility, and experience to secure the very best results for our clients. We represent major corporations, public entities, and individuals in a variety of complex business disputes, mass tort litigation, insurance recovery disputes, employment and wa ...
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📑 A clinical-stage biotechnology company based in San Francisco, backed by Third Rock Ventures, is harnessing the power of adipocyte biology and the latest advances in human genetics to develop first-in-class, next-generation medicines for cardiometabolic diseases. The company is building a pipeline of therapies that target rare and common cardiometa ...
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📑 Medical device company with a novel structural heart device is seeking an experienced PM to join their team as they begin First-In-Human Clinical Studies in the U.S.The PM will oversee the development and execution of clinical research studies, manage research sites, develop and maintain successful working relationships & implement project scope, d ...
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📑 Location: East Coast, USThis role is only open to candidates that already have the right to work in the US. No sponsorship available.The CompanyWe are partnered with a leading global biopharma company that is transforming the lives of patients with rare disease through a novel class of medicines. Having delivered the world's first and only approved ...
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📑 Hybrid position located in San Diego, CA Candidates are expected to manage and oversee all study-level vendor and site related activities and issues related to one or more clinical trials, as needed. The successful candidate must have experience managing Phase I-III trials and a good knowledge of clinical operations, GCP, and FDA regulatory environ ...
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📑 Director, Clinical Development - Immunology*Remote for East Coast Candidates*Meet has partnered with a well-established pharma based on the East Coast! They are looking for a Director of Clinical Development to join their immunology department. This position will be reporting into a Senior MD and will be supporting multiple global clinical programs ...
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📑 Our client is a biopharmaceutical company with marketed product, a robust pipeline and solid financials, focused in the Rare Disease area. They are currently seeking a Director or Senior Director of Biostatistics (depending on experience) to be responsible for statistical activities supporting clinical trials, including contributing to trial design ...
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📑 Part Time 20 hours per weekThe resource will be screening and enrolling subjects in trials.Must have an MD, experience in screening and enrolling subjects in clinical trials.Job SummaryPlans and directs all aspects of an organization's medical policies, standards, and programs. Responsible for strategic clinical relationships with physicians and in ...
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📑 ABOUT MACRO TRIALSMacro Trials is the precision research clinical platform, driving increased research velocity and an amplified patient experience to unlock value for all stakeholders in the clinical trial ecosystem. Via its digitally powered infrastructure and hub-and-spoke distributed model, Macro partners with pharmaceutical companies, CROs, ...
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📑 THE COMPANY89bio is a clinical-stage biopharmaceutical company focused on the development and commercialization of innovative therapies for the treatment of liver and cardio-metabolic diseases. The company's lead product candidate, pegozafermin (BIO89-100), is a specifically engineered glycoPEGylated analog of FGF21. Pegozafermin is being developed ...
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📑 Our client develops and commercializes therapies for hallucinations and delusions associated with Parkinson’s disease.Position Summary:Responsible for managing assigned Research and Development (R&D) Quality Risk Management activities including assessment and quality control of clinical trials' execution in a Good Clinical Practices (GCP) regulated ...
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📑 Title: Director/Senior Director of Regulatory Salary: $200,000 to $270,000Summary: An Oncology based biotech client of ours is looking to fill their Director/Senior Director role based out of their facility in the San Francisco Bay Area. They are looking for very committed and passionate candidates who can collaborate with their colleagues to help ...
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📑 Our client is a reputable, mid-sized regional firm seeking a mid-level to senior litigation associate to support their public law practice handling municipal, public works, environmental, and legislative matters. Schedule: Hybrid, 3 days in office; billable requirement of 1850 annually.Location: Downtown Los AngelesFirm Profile: Previous candidates ...
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📑 Study Responsible PhysicianOngoing ContractPart Time Hours: 10-20 hours a week RemoteEducation and Experience:University degree - MDPreferably experience in drug/clinical development and/or registry, surveillance studies (e.g. Project Management, Pharmacovigilance, Medical Affairs, RWE, Clinical Pharmacology, study operations)Post-marketing surveil ...
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📑 We are hiring a remote Research Grants Payment Collector to work for an oncology research institute in California. If you're looking to grow your career in a community-based company apply below!Ensure that Sponsor/CRO is providing payment per the terms in the clinical trial agreementsGenerate accurate and timely invoices for sponsors based on contr ...
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📑 Description :• Works on assigned studies to ensure that human subject protection is maintained, Good Clinical Practice (GCP), and applicable regulations are followed. • Coordinates and manages clinical site monitoring responsibilities for assigned studies in accordance with contractual agreements, SOPs, and applicabl ...
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📑 Job Title: Director of Clinical ResearchJob Summary:The Director of Clinical Research is responsible for leading and managing all aspects of clinical research initiatives within the organization. This role involves strategic planning, protocol development, project management, staff supervision, and ensuring compliance with regulatory standards. The ...
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📑 Senior/Executive Medical Director, Pharmacovigilance / Drug SafetyJob Ref : RWIBSMDLocation: RemoteSalary: Competitive Type: Permanent / Full Time RBW Consulting are partnered exclusively with a rapidly growing biotech company based in the New Jersey region. This exciting Oncology organization have had great success already in the clinic, with stro ...
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📑 Hiring an Associate Director BiostatisticsLocation: Fully Onsite in MarylandCompany: Mid-Size PharmaQualifications:PhD in Statistics or Biostatistics5+ years of Pharma Clinical Trial ExperienceProgramming Skills: SAS, and R/S LanguageAbility to work cross-functionally between departments.Responsibilities:Provide in-depth knowledge of clinical trial ...
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📑 A pharmaceutical company in New Jersey is looking to add a new Senior Pharmacovigilance Associate to their growing team. In this role, the Senior Pharmacovigilance Associate will be responsible for monitoring, processing, controlling, and reporting individual case safety reports and aggregate safety reports for company products.Responsibilities:The ...
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📑 We are a highly respected, multi state litigation firm in the Tri State Area. We are seeking a Junior Partner or Senior Associate Attorney to join our growing team. We offer a hybrid work environment and room for growth.Must Have: License to practice in new York, NJ license a plus.Responsibilities:Handle a caseload of insurance defense litigation m ...
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