Our world is transforming, and PTC is leading the way.Our software brings the physical and digital worlds together, enabling companies to improve operations, create better products, and empower people in all aspects of their business. Our people make all the difference in our success. Today, we are a global team of nearly 7,000 and our main objective is to create opportun

Perform net payment forecasting, inventory levels tracking, scheduling and coordinating currency and coin shipments, and collaborating with Board of Governors and U.S. Mint stakeholders. Collect, model, analyze, and interpret sophisticated and/or broad data; identify and interpret trends and patterns in datasets to locate influences. Prepare and present a variety of opera

No supervisory responsibilities. Normally receives general instructions on routine work, detailed instructions on new projects or assignments. Qualifications QUALIFICATIONS A M.S. or B.S. with a major in Biology or Chemistry preferred. Minimum 2 4 years of experience in a professional, experimental biology laboratory. Experience with techniques in molecular biology, cell

Research Technician No supervisory responsibilities. Normally receives detailed instructions on all work. Qualifications The ideal candidate should possess strong communication and organizational skills, attention to detail, and the ability to perform in a team environment. An interest in pursuing advanced education in MD, PhD, or MD PhD programs in the future is preferre

The Research Project Manager I will work independently under general supervision of a Principal Investigator, Research Scientists and/or higher level Research Project Managers. This position may be responsible for some or all of the following Responsible for day to day oversight and management aspects of assigned projects according to protocol specifications (may include

Administrative Assists principal investigator with protocol development. Assists principal investigator as appropriate with the Institute's protocol review process. Assists the principal investigator in developing the protocol budget. Collaborates with the Dana Farber Harvard Cancer Center DFHCC quality assurance of clinical trials office in developing protocol specific m

Regulatory Compliance Prepares and submits all protocol applications, amendments, continuing reviews, and informed consent documents for SRC and IRB review and approval 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 A

With direct supervision, the Referral Specialist Manages referral and authorization information as assigned through daily work queues and documents activities into the hospital information system; may require contacting physician offices and/or payors for referrals and authorizations via phone calls and/or websites. Ensures accurate and timely responses to all referral re

PRIMARY DUTIES AND RESPONSIBILITIES Provides image consulting services for Cancer patients to include patient consultation and patient education. Provides initial patient consultation and development of individualized appearance plan post surgery. Identifies resources to assist client with appearance normalization. Direct on hands contact with patients, taking measurement

Oversight of the clinical trials start up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site activation activities. Responsible for data reporting and management, collection of source documents, use and development of case report forms, adverse events reporting, filing and archiving of study records, and resolution of d

Provide administrative support to Research Nurses in clinic setting. Responsible for basic clinical trial document preparation (informed consents, study drug diaries, surveys (electronic/paper), research specimen kits, etc.) Administer clinical trial related surveys and use validated tools to assess a trial participant's functional and cognitive abilities as required by t

Screen patients for protocol eligibility, obtain informed consent, and register study participants to cohort studies. Interact with study participants as directed/required by the protocol and/or study team. Review and abstract clinical information from medical records for patients into departmental databases upon study enrollment and follow up. Verify data for quality and

To maintain close communication with the supervisor on matters pertaining to the policies and procedures of the laboratory. To assist the supervisor in scheduling, inventory, preparation of payroll information, development of new procedures, quality control, continuing education and quality improvement activities. To assist the supervisor in conducting annual performance

Clinical Trials Operations Assistant Clinical Research Managers (ACRM) will be responsible for assisting the Clinical Research Manager with the oversight of their disease group's clinical trial portfolio and all related regulatory and compliance requirements. The ACRM will assist the CRM will all aspects of study start up, active and close out activities for the group's p

Perform Construction Inspections of contractor activities. Contractors activities include, but may not be limited to, the following Soils Reinforcing Steel Bars Concrete Masonry Hot Mixed Asphalt (HMA) Coordinating and monitoring of sampling, testing, and reporting activities to provide operational consistency, resolve discrepancies, and meet testing frequency requirement