Clinical Trial Assistant or Associate Clinical Trial Manager to join our client based in Waltham. Clinical Trial Assistant / Associate CTM. Responsible for trial related activities from startup to close-out of a clinical trial in close collaboration with internal stakeholders and CROs. Drive the ope...
The Administrative Assistant performs general administrative office assignments, medical record keeping, and functions as a communication link to and within the healthcare unit as appropriate. VitalCore Health Strategies (VCHS), an industry leader in Correctional Health Care has openings for a Full ...
This is a grant-funded Research Assistant position in the Department of Comparative Pathobiology within the laboratory of Dr. Collaborate with other research staff members to develop and implement novel research methods. The Department of Comparative Pathobiology at Cummings School of Veterinary Med...
Candidates with prior administrative support experience within the military have shown success in this role. ...
The person will be responsible for processing drawings, RFI submittals and project documentation, coordination on all new build projects within energy supply's strategic projects group; new wind farms, solar projects, repowers and other major capital projects. We are searching for a Project Coordina...
Responsible for assisting the Construction Purchasing Manager in preparing the “Take-Off” or “Equipment” list and ordering the correct equipment needed for a project. To Manage the Schedule, Scope, and Budget of assigned Capital & Expense Construction Projects. Coordinate and Direct General Contract...
Reporting to the Director, Clinical Operations, the Senior Clinical Trial Manager is responsible for leading the execution of clinical studies on schedule and on budget. The Senior Clinical Trial Manager ensures studies are conducted efficiently and with quality, adhering to timelines and budget, an...
The CTA position will assist with daily clinical trial execution activities including the coordination of documents associated with the conduct of investigational clinical studies. The CTA will support the Clinical Trial Managers in day-to-day activities including engaging vendors, starting up and m...
The Project Manager leads projects from inception to completion and may perform the role of EPC Project Manager or Program Manager, as well as provide guidance to others performing these roles as required by the specific project. Job Title: Project Manager / Assistant Project Manager. The Project Ma...
Work with scientists to conduct lab-based studies to support project efforts.Perform tissue culture work with human cell lines to develop and optimize workflows for cell model engineering and in vitro screening.Support project management efforts in standard operating procedure creation, sharing know...
Senior Research Associate, Analytical Development Contractor (Core Testing/Characterization). Our research team is based in the heart of Cambridge, MA, and our Technical Development, Manufacturing & Quality team is based in our facility in Bedford, MA. ...
As a Project Manager, your fiscal and managerial oversight across all project facets ensures client satisfaction, effective resource allocation, and safe, timely completion of projects. This position can be either a Project Manager or a Senior Project Manager depending on experience. HVAC/building a...
Maintain the Trial Master File all clinical projects. Keep abreast of SOPs, Good Clinical Practice (GCP) and ICH guidelines as well as state and federal laws and ethical standards. Assemble and distribute regulatory binders to clinical sites. Draft and/or assist with preparation of trial-related doc...
The Clinical Trial Manager will be responsible forthe design, planning, execution and leadership of clinical studies and clinical programs worldwide for BSC's Coronary Therapies portfolio. Possesses a technical knowledge of products, processes, and regulatory requirements for clinical trials conduct...
Associate Clinical Trial Manager. Responsible for trial related activities from startup to close-out of a clinical trial in close collaboration with internal stakeholders and CROs. Drive the operational planning, content, execution, and delivery for one or more clinical trials. Support trial deliver...
At least 4 years of clinical research experience, including at least 2 years as a Clinical Research Associate (CRA) within the pharmaceutical/biotech or CRO industry. Acumen Pharmaceuticals is searching for a Senior Clinical Research Associate (CRA) to join our Clinical Operations team to implement ...
The Senior Clinical Trials Study Manager is primarily responsible for coordinating the execution of clinical trial projects including managing the scope, timeline and budget of assigned projects. This position will also have direct line management responsibility of junior level study management team...
As they continue to grow, they are seeking a highly experienced and motivated Lead Project Manager to join their dynamic team to work on ground up and renovations projects in the Academic, Public, and commercial sectors. Project Management: Oversee and lead multiple projects simultaneously from conc...
The purpose of the Fabrication Project Coordinator is to support the Fabrication and the repairs department with scheduling, procurement, coordination, customer service, invoicing, project details, cost reporting and departmental finance. Equipment and Fabrication Project Coordinator. The Fabricatio...
Job Title: Senior Structural Design Engineer / Project Manager. Senior Structural Design Engineer / Project Manager will hold a key leadership role within our team-oriented organization. We anticipate welcoming an individual who not only brings technical prowess but also supports and makes impactful...
Worldwide Clinical Trials (Worldwide), a leading global contract research organization (CRO), works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications – from discovery to reality. ...
Works with Clinical Trial Oversight Managers (CTOMs) and Clinical Study Team (CST) to manage site trends through dashboard review and ongoing risk assessment to ensure quality standards and address concerns associated with study delivery at sites within established protocols and portfolio under gene...
Reporting to the Senior Research Director, DigitalSystems, Operations and Quality Verification, the Research Assistant, TIMSS and PIRLS, assistswith ensuring the highest standards of operations and quality control in TIMSSand PIRLS. Research Assistant, TIMSS and PIRLS . TIMSS and PIRLS are sponsored...
Job Summary: We are seeking an experienced Executive Administrative Assistant to join our team at our Hudson, MA office. In this role, you will provide administrative support to the CEO of the company, this individual will get to know the business inside and out. Responsibilities include a var...