Talent.com

Document controller Jobs in Worcester, MA

Create a job alert for this search

Document controller • worcester ma

Last updated: 1 day ago

Clinical Research Coordinator - Open Rank

InsideHigherEdWorcester, Massachusetts, United States
Full-time

Under the direction of the Principal Investigator (PI) or designee, the Clinical Research Coordinator is responsible for independently performing delegated tasks and procedures involving human subj...Show more

 • Promoted

Medical Office Assistant

APDermWorcester, MA, United States
Full-time

Reporting to the Practice Manager, the Medical Office Assistant is responsible for interacting with patients in a healthcare setting and managing administrative tasks for the medical team.The Medic...Show more

 • Promoted

Licensed Practical Nurse - Behavioral Health - Worcester, MA

Precision HealthcareWorcester, MA, United States
Full-time

Current LPN license in Massachusetts.Experience in behavioral health or psychiatric nursing preferred.Strong communication and patient care skills.Ability to work independently in a fast-paced envi...Show more

Controller

Michael Page International Inc.Worcester, MA, United States
Full-time

Fast growing construction and contracting company.The client are a brilliant organization, with a fantastic working culture.They have grown at a strong rate over a number of years, and offer a wide...Show more

 • Promoted

Senior Accountant

SDL Search PartnersWorcester, MA, United States
Full-time

Metro-West company actively hiring a Senior Accountant to join a high-performing Accounting & Finance team.This role will be a mix of general ledger accounting, budget/variance analysis, and some F...Show more

Remote UI/UX SWE Experts - AI Trainer ($80-$100 per hour)

MercorWorcester, Massachusetts, US
Remote
Full-time

On this project, you will be asked to improve a given document, spreadsheet, or slide deck based on a pre-set style guide and then document all of the changes you made.You will be paid per task, no...Show more

Medical Office Assistant

My Derm RecruiterWorcester, MA, United States
Full-time

Reporting to the Practice Manager, the Medical Office Assistant is responsible for interacting with patients in a healthcare setting and managing administrative tasks for the medical team.The Medic...Show more

Remote Excel/PowerPoint/Document Style Experts - AI Trainer ($200-$400 per hour)

MercorWorcester, Massachusetts, US
Remote
Part-time

On this project, you will be asked to improve a given document, spreadsheet, or slide deck based on a pre-set style guide and then document all of the changes you made.You will be paid per task, no...Show more

Travel Patient Care Tech (PCT) - $1,350 to $1,450 per week in Pittsfield, MA

AlliedTravelCareersWorcester, Massachusetts, US
Full-time

Shift: 8hr Nights Monday-Friday 40hr gt.THIS NEED IS FOR AN AIDE IN THE RADIOLOGY DEPT/MRI.Years CURRENT MRI experience [required].GE Equipment experience [Required].Meditech Expanse experience [st...Show more

 • Promoted

Jr. Accounting Specialist

Atlas TechnicaWorcester, MA, United States
Full-time

Atlas Technica's mission is to shoulder IT management, user support, and cybersecurity for our clients, who are hedge funds and other investment firms.Founded in 2016, we have grown year over year ...Show more

Large Corrective Exchange (MCE) Technician

GEV Wind PowerWorcester, MA, US
Full-time

GEV Wind Power is seeking experienced.Large Corrective Exchange (MCE) Technicians.This role involves working at height to remove and install large wind turbine components such as blades, gearboxes,...Show more

Home Health Aide

Pathways HealthcareWorcester, MA, United States
Full-time

Pathways Healthcare Home Health Aide.Pathways Healthcare is a leading, physician- and nurse practitioner-led home health and hospice organization, committed to redefining recovery through comprehen...Show more

PT - Rehab - Travel

core hire llcWorcester, Massachusetts, US
Full-time

Provide skilled PT in accordance with state/federal regulations and facility guidelines.Responsible for evaluating patients, developing treatment and discharge plans, and delivering therapy to impr...Show more

Remote Tagalog Audio Generalist Evaluator Expert - AI Trainer ($50-$50 per hour)

MercorWorcester, Massachusetts, US
Remote
Full-time

Mercor is seeking a **Tagalog Audio Generalist Evaluator Expert** to contribute to a high-impact audio AI research project with a leading research lab.In this role, you will work on transcription, ...Show more

Quality Assurance (QA) Document Control Specialist II

Collins ConsultingWorcester, MA, United States
Full-time

Quality Assurance Document Management.This is a 100% onsite position.Assists in maintaining a compliant, efficient Quality Assurance Document Management program.Under direct supervision, perform da...Show more

Travel Nurse RN - Medical-Surgical - $2,188 per week in North Adams, MA

TravelNurseSourceWorcester, Massachusetts, US
Full-time

Registered Nurse (RN) | Medical-Surgical.TravelNurseSource is working with Mindlance Health to find a qualified Med/Surg RN in North Adams, Massachusetts, 01247!.ID: 75990078 Shift: Varied 0 hours ...Show more

 • Promoted

Physical Therapist Come join our in-house team. We have competitive wages

Shrewsbury Rehabilitation and Nursing at SouthgateShrewsbury, MA
Full-time

Shrewsbury Rehabilitation and Nursing at Southgate -.Physical Therapist Job Description.Graduate of an accredited university with a B.Doctorate, MA or MS in Physical Therapy that is recognized by t...Show more

Behavioral Health Technician

Promises Behavioral Health, Inc.Worcester, MA, United States
Full-time

The Behavioral Health Technician provides oversight and support services to clients and staff in a residential treatment facility for adults with co-occurring diagnoses.BHT are responsible for arou...Show more

MTM Pharmacist

Pharmacy CareersWorcester, MA, USA
Full-time +1

Redefine patient engagement through personalized, remote MTM services.Conduct telephonic or video MTM sessions for Medicare and commercial patients.Document clinical interventions and CMRs in compl...Show more

People also ask
The cities near Worcester, MA that boast the highest number of document controller jobs are:
Clinical Research Coordinator - Open Rank

Clinical Research Coordinator - Open Rank

InsideHigherEdWorcester, Massachusetts, United States
30+ days ago
Job type
  • Full-time
Job description
Overview

POSITION SUMMARY:

Under the direction of the Principal Investigator (PI) or designee, the Clinical Research Coordinator is responsible for independently performing delegated tasks and procedures involving human subject research. This work includes coordination of regulatory activities and aspects of collection and management of data for research protocols related to treatment, ancillary services, and prevention practices.

This is an open-rank posting (there are 4 levels of Clinical Research Coordinator) - candidates will be hired into the level commensurate with their experience.

Responsibilities

ESSENTIAL FUNCTIONS:

Clinical Research Coord I:

  • Obtain consent of research participants in accordance with the IRB approved protocols and all applicable regulations including HIPAA
  • Identify, schedule and/or conduct participant study visits, tests and/or interviews/telephone follow up calls
  • Coordinate participant remuneration/compensation per protocol
  • Maintain all regulatory documentation, including local or central IRB and study data. Provide data/support to study Investigators, sponsors and/or external monitors/auditors
  • Identify issues with protocol compliance. Keep principal investigator and manager aware of any issues regarding compliance
  • Document and collect data and/or samples for research related procedures performed during participant study visits.
  • Ensure clinicians and/or PI accurately document their study activities according to protocol
  • Track and maintain study enrollment and completion of milestones
  • Assist with financial /operational aspects of grant and contracts. May be responsible for clinical research billing review within the required timeframe.
  • Track and maintain study related information in the data management system within the required timeframe
  • Responsible for monitoring the inventory of research related supplies
  • Participate in grant preparation, manuscript writing, data presentations and Institutional Review Board (IRB) processes
  • Provide detailed written summaries from literature searches and related sources to serve as a resource for the study team and clinicians/PIs
  • Present study status reports related to assigned research projects
  • Participate in the design, development, and documentation of study related data and collection tools, (e.g. questionnaires, treatment data and/or therapeutic checklists)
  • Maintain strict adherence to all study protocols, including all regulatory requirements adhering to appropriate federal, local and institutional guidelines.
  • Comply with all safety and infection control standards appropriate to this position
  • Adhere with established policies, health and safety regulations and requirements, procedures, and department objectives
  • Adhere to Good Clinical Practice (GCP) guidelines and all human subject protection practices
  • Must practice discretion and adhere to school and hospital confidentiality at all times
  • Perform other duties as required.

Clinical Research Coord II

Duties noted above plus:

  • Conduct preliminary quality assurance reviews of study data
  • Contribute to data presentations and Institutional Review Board (IRB) processes
  • Track and maintain study related information in the data management system within the required timeframe
  • Contribute to the design, development, and documentation of study related data and collection tools, (e.g. questionnaires, treatment data and/or therapeutic checklists)
  • Document and collect data/ samples for research related procedures performed during participant study visits. Ensure clinicians and/or PI accurately document their study activities according to protocol.
  • Monitor strict adherence to all study protocols, including all regulatory requirements adhering to appropriate federal, local and institutional guidelines. Identify and resolve issues with protocol compliance. Keep principal investigator and manager aware of any issues regarding compliance

Clinical Research Coord III

Duties noted above plus:

  • Assist with recruiting, screening, selecting, maintaining and terminating study subjects for multiple protocols
  • Ensure accuracy and completion of all regulatory documentation, including local or central IRB and study data. Provide data/support to study Investigators, sponsors and/or external monitors/auditors
  • Direct the activities of research support staff. Assist with the training of staff
  • Develop preliminary designs for study related documentation of data and collection tools, (e.g. questionnaires, treatment data and/or therapeutic checklists)
  • Contribute to grant preparation, assessment of protocol feasibility, manuscript writing, data presentations and Institutional Review Board (IRB) processes

Sr Clinical Research Coord

Duties noted above plus:

  • Responsible for internal review/monitoring of clinical data for quality assurance purposes. Reports findings
  • Responsible for the smooth operation of all assigned studies on a day-to-day basis, interacting with investigators, staff members, clinicians, sponsors, etc. to ensure project timelines and goals are met
  • Contribute independently to the development of preliminary designs for study related documentation of data and collection tools, (e.g. questionnaires, treatment data and/or therapeutic checklists)
  • May Supervise the activities of research support staff. Assist with the selection, training, and supervision of staff
  • Prepare ongoing summary reports from various data sources, and collaborate with investigators on data presentation, interpretation, and the writing of manuscripts for publication and grant proposals
  • Identify and resolve issues with protocol compliance. Keep principal investigator and manager aware of any issues regarding compliance
  • Accountable for quality assurance reviews of study data
  • Assist with financial /operational aspects of grant and contracts. Responsible for clinical research billing review within the required timeframe.
  • Contribute independently to grant preparation, assessment of protocol feasibility, manuscript writing, data presentations and Institutional Review Board (IRB) processes

Qualifications

REQUIRED QUALIFICATIONS:

Clinical Research Coord I:

  • Bachelor’s degree in a scientific or health related field, or equivalent experience
  • 0-1 year of related experience
  • Ability to travel off site locations

Clinical Research Coord II:

  • Requirements noted for CRC I plus:
  • 1-3 years of related experience

Clinical Research Coord III:

  • Requirements noted for CRC I plus:
  • 3-5 years of related experience

Sr Clinical Research Coord:

  • Requirements noted for CRC I plus:
  • 5-7 years of related experience
  • Demonstrated knowledge of quality management principles in a scientific or hospital setting
Additional Information

#LI-KR1