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Accounting Jobs in Casco, MI

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Sr. Clinical Research Associate Getinge AB

Waltham, MA

With a firm belief that every person and community should have access to the best possible care, Getinge provides hospitals and life science institutions with products and solutions aiming to improve clinical results and optimize workflows. The Senior Clinical Research Associate will report to the VP Scientific and Medical Affairs and will play an important role in study data management and overall clinical operations of the prospective randomized studies.

30+ days ago

Clinical Trial Project Manager Job Vision Source LP

Worcester, MA

Track Clinical Trial Agreement execution status at each site and coordinate with participating sites'' research administration offices Maintain the regulatory binder/eRegulatory system: protocol versions, informed consent forms, IRB approvals and amendments, training records, and delegation logs Track participant enrollment progress at each site against targets Perform direct data collection responsibilities for the lead site Coordinate device and supply logistics to participating sites (fitting kits, tape supplies, recording devices, prescription lens orders) Support internal and external reporting, including sponsor progress reports Contribute to results dissemination, including manuscript and conference preparation support Grant reporting Grant preparation and submission for future projects Identification of new clinical trial site opportunities for the practice. Clinical Trial Project Management Duties (Primary Focus) Assist the Principal Investigator in the overall day-to-day management of the multicenter trial Coordinate patient recruitment and enrollment activities across all participating sites Track protocol adherence across sites and help resolve protocol deviations Coordinate the schedule of study visits and monitor enrollment/visit-completion timelines against the study''s schedule of events Manage data transfer between participating sites and the coordinating site, and support preparation of data for analysis Prepare and maintain data collection instruments Assist with regulatory approvals, IRB reliance/authorization agreements, and clinical trial registration (e.g., ClinicalTrials.gov)

10 days ago

Senior Clinical Trial Specialist (Contract) Centessa Pharmaceuticals, LLC

Boston, MA

$65–$85 / hour

Assists in tracking key site metrics and milestones such as Site Initiation Visits and site activation, subject recruitment and enrollment, critical study dosing days and assessments, scheduled Monitoring Visits and Close-Out Visits etc. Centessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and Company, is a clinical-stage company developing orexin receptor 2 (OX2R) agonists as a new class of medicines for the treatment of narcolepsy and potentially other sleep-wake disorders.

30+ days ago

Clinical Trial Manager Seaport Therapeutics

Boston, Massachusetts

The ideal candidate will embrace a collaborative, innovative culture that embodies our values of service to patients impacted by mental health conditions, with a “we own it” mentality, demonstrating entrepreneurial spirit and technical excellence while fostering teamwork and continuous improvement. All the therapeutic candidates in its pipeline of first and best-in-class medicines are based on the Glyph platform, which is uniquely designed to enable oral bioavailability, bypass first-pass metabolism and reduce hepatotoxicity and other side effects.

30+ days ago

Clinical Contracts Manager, Cambridge, MA Isomorphic Labs

Cambridge, MA

Operating at an organizational level, this role drives vendor selection, supports negotiation of Master Service Agreements (MSAs) and Clinical Trial Agreements (CTAs), and manages vendor related study budgets and contract lifecycle activities. By harnessing AI’s powerful capabilities, we can use it to model complex biological phenomena to help design novel molecules, anticipate how drugs will perform and develop innovative medicines to treat and cure some of the world’s most devastating diseases.

30+ days ago

Clinical Project Manager Relay Therapeutics, Inc.

Cambridge, MA

$102,000–$145,000 / year

Develop and maintain strong working relationships with internal and external stakeholders (cross-functional team members, Contract Research Organizations (CROs), external experts, and clinical site staff), ensuring high-quality services are executed in a timely and cost-effective manner. Experience managing global clinical trials and study teams across all stages (startup-closeout) of phase I-III studies and a strong working knowledge of GCP/ICH and other applicable regulations/guidelines required.

30+ days ago

Executive Director, Head Of Clinical Development - Oncology Lantheus Holdings, Inc.

Bedford, MA

$206,000–$381,000 / year

Lantheus (NASDAQ: LNTH) is the leading radiopharmaceutical-focused company, delivering life-changing science to enable clinicians to Find, Fight and Follow disease to deliver better patient outcomes. Through recent acquisitions, along with strategic partnerships across the life sciences ecosystem, we are accelerating our efforts to advance precision medicine and improve patient outcomes around the world.

30+ days ago

Clinical Research Coordinator to Home Based CRA (Clinical Research Associate) Medpace Holdings Inc

Boston, MA

Remote

On-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward. When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.

30+ days ago

Temporary Clinical Research Coordinator Whoop Inc

Boston, MA

You will coordinate day-to-day study activities, support participants and research sites, maintain study documentation and tracking tools, and help ensure that study procedures are completed accurately and on time. Collaborate with Clinical Operations, Clinical Science, Clinical Research Associates, Data Management, Regulatory, Quality, investigators, research sites, vendors, and other cross-functional partners.

30+ days ago

Clinical Project Manager Relay Therapeutics Inc

Cambridge, MA

$102,000–$145,000 / year

30+ days ago

Senior Product Manager - Veeva Clinical Operations Veeva Systems

Boston, MA

Remote

$120,000–$200,000 / year

Unlike a traditional corporation, whose only legal duty is to maximize shareholder value, PBCs consider their public benefit purpose and the interests of those materially affected by the corporation's conduct-including customers, employees, and the community-in addition to shareholders' interests. We're not just any public company - we made history in 2021 by becoming a public benefit corporation (PBC), legally bound to balancing the interests of customers, employees, society, and investors.

30+ days ago

Associate Director, Clinical Operations Site Engagement Lead CSL Plasma

Waltham, Pennsylvania

$186,000–$220,000 / year

Working in close collaboration with Clinical Development, Clinical Trial Management, Site Management, Feasibility, Start-up, Medical Affairs, and other functions, the Associate Director, Site Engagement Lead builds trusted relationships with investigators and institutions while driving internal alignment, informed decision-making, and continuous improvement. The role serves as a voice for clinical sites within CSL , ensuring that site perspectives, operational realities, and external intelligence are translated into actionable insights that improve study feasibility, site selection, recruitment, retention, study execution, and the overall site experience.

3 days ago

Clinical Research Coordinator I with Translational Research Lahey Hospital and Medical Center

Burlington, MA

$21.64–$26.50 / hour

Submits all IRB submission documents such as protocol amendments and consent form revisions, annual reviews, adverse events, investigator changes, accrual status change and change in risk to the IRB in a timely manner with moderate assistance/guidance from senior staff; Complies with IRB decisions, conditions and requirements. Completes source worksheets and case report forms (CRFs) as dictated by the assigned research study (i.e. required forms in the required format in the required time interval); Ensures CRF's and source are complete and done correctly.

2 days ago

Clinical Trial Manager Repertoire Immune Medicines

Cambridge, MA

$112,000–$160,000 / year

The DECODE platform has been validated through four strategic partnerships with leading pharmaceutical companies—Bristol Myers Squibb, Genentech, Eli Lilly, and Pfizer—representing over $4.5 billion in disclosed total deal value and $185 million in upfront payments received to date. Clinical Trial Manager Role Overview We are seeking an experienced Clinical Trial Manager to provide both strategic leadership and hands-on oversight of early-stage oncology trials, including first-in-human trials.

30+ days ago

Clinical Pharmacist, Central Pharmacy Operations, 32hr, Day UMass Memorial Health Care Inc

Worcester, MA

$98,862.40–$177,944 / year

Major Responsibilities: The following key performance areas (Clinical, Operations/Distribution, Financial, Safety and Regulatory, Research and Education) are performed by the clinical pharmacist: Clinical Performance: Provides medication management services in a collaborative manner that consist of the following: Review patient medication history, educate patients on drug therapy, establish desired outcomes, develop/modify therapeutic plans, determine alternatives for achieving outcomes, develop drug monitoring plans, monitor patient outcomes, document medication related issues in electronic health record, interpret laboratory data, review patient medication profiles, monitor pharmacokinetics of drug therapy, monitoring for potential adverse drug - drug, drug-lab, drug-disease state, and drug - food interactions. Research and Education Performance: Precepts Intermediate Pharmacy Practice Experience (IPPE) rotation students, and Advanced Pharmacy Practice Experience (APPE) rotation students, and pharmacy residents consistent with academic credentials and clinical experience.

5 days ago

Clinical Research Coordinator II- Cardiology Lahey Hospital and Medical Center

Burlington, MA

$23.08–$28.85 / hour

Customer 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. Extracts data on protocol subjects from hospital records, outpatient charts and private physician office records in order to complete case report forms required by specific protocols.

2 days ago

Regulatory Coordinator II - Clinical Trial Office Dana-Farber Cancer Institute Inc

Brookline, MA

Remote

$61,110–$67,900 / year

This position will work collaboratively with a variety of personnel at all levels, including faculty and study team members of DF/HCC and external institutions, cooperative groups, clinical trials experts, representatives from the pharmaceutical industry, federal agencies, and other research organizations. Prepares and submits regulatory documentation that may include IND/IDE applications, FDA annual reports, Serious Adverse Event reports, to the appropriate regulatory agencies including the Food and Drug Administration (FDA), Office of Biotechnology Activities (OBA), etc.

30+ days ago

Senior Clinical Research Coordinator Brigham and Women's Hospital

Boston, MA

The framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success. In addition to competitive base pay, we offer comprehensive benefits, career advancement opportunities, differentials, premiums and bonuses as applicable and recognition programs designed to celebrate your contributions and support your professional growth.

22 days ago

Director of Clinical Research Eight Sleep

Boston, Massachusetts

You will also own program management across the full breadth of the clinical team's verticals — hardware studies, AI/ML development studies, and women’s sleep studies — while also acting as Eight Sleep's public-facing voice on the science of sleep, from peer-reviewed publications to press and podcast appearances. Provide scientific input on marketing claims, press releases, and journalist articles by reviewing web, social, and app content for accuracy and ensuring every public-facing claim and document is backed by data.

30+ days ago

Senior Manager, Clinical Scientist Replimune Group, Inc.

Woburn, MA

$159,000–$205,500 / year

The RPx platform is designed to have a unique dual local and systemic activity consisting of direct selective virus-mediated killing of the tumor resulting in the release of tumor derived antigens and altering of the tumor microenvironment to ignite a strong and durable systemic response. Director Clinical Scientist, ensures the successful execution of clinical development programs and deliverables in partnership across the organization, with external vendors, and with external academicians and collaboration partners.

30+ days ago

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Accounting Jobs in Casco, MI

Sr. Clinical Research Associate Getinge AB

Clinical Trial Project Manager Job Vision Source LP

Senior Clinical Trial Specialist (Contract) Centessa Pharmaceuticals, LLC

Clinical Trial Manager Seaport Therapeutics

Clinical Contracts Manager, Cambridge, MA Isomorphic Labs

Clinical Project Manager Relay Therapeutics, Inc.

Executive Director, Head Of Clinical Development - Oncology Lantheus Holdings, Inc.

Clinical Research Coordinator to Home Based CRA (Clinical Research Associate) Medpace Holdings Inc

Temporary Clinical Research Coordinator Whoop Inc

Clinical Project Manager Relay Therapeutics Inc

Senior Product Manager - Veeva Clinical Operations Veeva Systems

Associate Director, Clinical Operations Site Engagement Lead CSL Plasma

Clinical Research Coordinator I with Translational Research Lahey Hospital and Medical Center

Clinical Trial Manager Repertoire Immune Medicines

Clinical Pharmacist, Central Pharmacy Operations, 32hr, Day UMass Memorial Health Care Inc

Clinical Research Coordinator II- Cardiology Lahey Hospital and Medical Center

Regulatory Coordinator II - Clinical Trial Office Dana-Farber Cancer Institute Inc

Senior Clinical Research Coordinator Brigham and Women's Hospital

Director of Clinical Research Eight Sleep

Senior Manager, Clinical Scientist Replimune Group, Inc.

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