Clinical Trial Admin & TMF Coordinator
Galderma
Galderma is seeking a Clinical Trial Administrator based in Boston, MA. The role involves managing the Trial Master File, supporting clinical teams through administrative tasks, and ensuring regulatory compliance for clinical trials. Ideal candidates should have a Bachelor's Degree and 3+ years of experience in clinical administration. You will work closely with vendors and regulatory bodies in a dynamic environment that values diversity and inclusion. #J-18808-Ljbffr
- ...Cambridge, Massachusetts is seeking a qualified professional to manage the clinical Trial Master File (TMF) and ensure compliance with regulatory policies. The successful candidate will coordinate TMF quality checks, manage study expenses, and maintain accurate study...Suggested
- ...divh2TMF Documentation Coordinator/h2pA Few Words About Us - Integrated... ...Information Technology (IT), Clinical Research, Rehabilitation... ...Writing documentation required for Trial Master Files./ppUploads/files... ...ensuring timely filing of TMF documentation; addressing backlog...Suggested
$61.11k - $67.9k
...The Regulatory Coordinators (RC) works under the direction of the Principal Investigator(s), Regulatory Operations Manager, Clinical Research Manager and / or directly for the Clinical Trials Office to complete the regulatory requirements of the clinical research project...SuggestedWork at officeLocal area$48.1k - $54.4k
...Dana-Farber Cancer Institute is seeking a Clinical Research Coordinator (CRC) to support clinical trials focused on Breast Oncology. The CRC will manage patient data and ensure compliance with research protocols. This role involves overseeing clinical trial processes,...Suggested- ...Document Coordinator A Few Words About Us - Integrated Resources, Inc is a premier staffing... ...areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing... ...of documents to clinical study Trial Master File and QC of Trial Master File,...SuggestedWork at office
$48.6k - $54.5k
...Protocol Activation Coordinator I The Protocol Activation Coordinator I represents Nursing and Patient Care Services in the operational review and activation of clinical trials across DFCI sites. The Protocol Activation Coordinator I translates protocol requirements...Full timeWork at office10 hours per weekShift workWeekday work- ...Protocol Activation Coordinator II The Protocol Activation Coordinator (PAC) II represents Nursing and Patient Care Services in the operational review and activation of clinical trials across DFCI sites. The Protocol Activation Coordinator II translates protocol requirements...Full timeWork at office10 hours per weekShift workWeekday work
$55.53k - $61.7k
The Regulatory Coordinators (RC) works under the direction of the Principal Investigator(s), Regulatory Operations Manager, Clinical Research Manager and/or directly for the Clinical Trials Office to complete the regulatory requirements of the clinical research project...Work at officeLocal area$61.11k - $67.9k
Dormont Manufacturing Co in Brookline, Massachusetts, seeks a Regulatory Coordinator to manage regulatory tasks for clinical trials. You will work closely with diverse teams to ensure compliance with regulations and prepare necessary documentation for studies. The ideal...$55.53k - $61.7k
Dormont Manufacturing Co is seeking a Regulatory Coordinator in Boston to oversee the regulatory requirements for clinical research projects. This role involves preparing submissions, maintaining regulatory files, and ensuring compliance with federal regulations. Ideal...$39.14 - $101.14 per hour
...you’re making a difference in people’s lives.Registered Nurse Coordinator – Hematology OncologyLank Cancer Center | Beth Israel... ...model for seamless navigationInnovation and growtho Access to clinical trials and emerging therapieso Stay at the forefront of oncology practicePurpose...Hourly payPart timeShift work- ...all levels and functional areas of GPSRM and partner with the clinical development as well as Data Management teams. The exceptional candidate... ...governing both Safety reporting and processing for clinical trial environments highly preferred Experience in managing...Flexible hours
- ...conventions and coding process Qualifications General Knowledge & Skills: • Safety experience coding safety cases. • Clinical trial experience in coding • 2-5 years medical coding using the MedDRA and WHO Drug dictionaries as well as the structure and function...
- ...directly to the Billing Manager and works closely with the School Clinic it supports: Postgraduate Prosthodontics Clinic. Revenue Cycle... .... What You'll Do Under limited supervision, the Insurance Coordinator: Checks patient insurance eligibility, benefits, limitations and...
- ...Boston Medical Center is seeking a Clinical Research Regulatory Coordinator for the Cancer & Hematology Clinical Research Program. This role involves coordinating regulatory documentation, protocol submissions, and compliance with all applicable regulations. The ideal...
- ...with medicine, with access to training in dental specialties. Clinics managed at TUSDM provide quality comprehensive care to more than... .... What You'll Do Under minimal supervision, the Clinical Coordinator provides advanced clinical support and communications for the...Work at officeImmediate start
$64.48k - $86.24k
...Beth Israel Lahey Health, Inc. is seeking a full-time Program Administrator for Clinical Research Programs in Boston, MA. This role involves overseeing strategic planning and operational execution of clinical research operations and providing administrative support for...Full timeWork experience placement$55.53k - $61.7k
A prominent cancer research institution in Boston seeks a Regulatory Coordinator to manage submissions and compliance for clinical research projects. The person will collaborate with various stakeholders including faculty and study team members. Key responsibilities include...$78.58k - $117.86k
...Description: I. Position Summary: Plan, organize, develop and coordinate MDS Assessment Process. Assure compliance with all state and federal MDS transmission requirements. Collaborate with clinical and administrative staff regarding issues relative to the Resident...Full timeRemote work- ...compassion - must guide what we do, as individuals and professionals, every day. Works Under The Supervision Of The Nurse Manager/Clinical Coordinator. The Registered Nurse (Rn) Assesses, Plans, Implements, Evaluates And Supervises Individual Patient Care On A Nursing Unit/...Temporary workFlexible hours
- ...in the Department of Environmental Health is seeking a Program Coordinator for the Occupational and Environmental Medicine Residency (... ...The OEMR Program is a two‑year training program that includes clinical and research training in both years and an MPH degree in Occupational...Part timeWork at office
$87.5k - $93k
...malignancy studies. We are looking for a TMF Coordinator to support these studies. The ideal... ...should have relevant experience in oncology clinical studies and should thrive in a fast-... ...Responsibilities: Support day-to-day Trial Master File (TMF) activities for...Work at officeLocal areaFlexible hours- ...Alcanza is a growing multi-site, multi-phase clinical research company with a network of... ...first phone call to the last visit of the trial. Key Responsibilities Essential... ...payments following visit completion; Coordinates / schedules transportation for volunteers...Full timeTemporary workWork at office
- ...supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a... ...device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global...Full timeLocal areaRemote work
$21 - $28.26 per hour
...dynamic and compassionate team member to join our growing Urgent Care practice located in the vibrant Chestnut Hill Square Plaza. Our clinic is in a prime street-level storefront location at 200 Chestnut Hill Square, conveniently situated near SoulCycle. The complex...Hourly payShift work$21.76 - $36.24 per hour
...Clinical Practice Assistant Requisition Number: 11106 Pay Range: $21.76 - $36.24 per hour Location: CHA Malden Care Center Work Days: Various shifts including evenings and Saturdays Category: Medical Assistant Department: Malden Family Health Center...Hourly payFull timeWork experience placementLocal areaShift workDay shiftAfternoon shift- ...Clinical Research Coordinator Primary Duties and Responsibilities: • Ensures proper patient identification and maintains patient safety, privacy, confidentiality and follows guidelines under HIPAA. • Obtains and records vital signs, pain screens, weights and heights...
$21 - $28.26 per hour
...growing BILH team, you're not just taking a job, you're making a difference in people's lives. Performs both administrative and clinical functions to support smooth and efficient practice operations, while contributing to BIDMC's promise of providing extraordinary...Hourly payWork experience placementInterim roleImmediate startShift work$21.76 - $36.23 per hour
...Clinical Practice Assistant - Reproductive Health Requisition Number: 11711 Pay Range: $21.76 - $36.23 per hour Location: CHA Broadway Care Center Category: Medical Assistant Department: Reproductive Health Job Type: Per Diem Union Name : CH Laborers...Hourly payDaily paidWork experience placementLocal areaShift work$50k - $70k
Patient Recruitment Coordinator About Research Grid: Research Grid (R.grid) is the automation engine for admin-free clinical trials. Our mission is to enable faster, more successful clinical trials by engineering smart software that safely automates back-office admin across...Full timeContract workWork at officeRemote work
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