Clinical Research Manager jobs in Connecticut
Clinical Research Manager manages the clinical monitoring process and the administration of clinical trials. Supervises CRAs in in-house and on-site monitoring, filing, and clinical trial administration. Being a Clinical Research Manager oversees adherence to SOPs, Good Clinical Practice and FDA regulations. Helps with the development and implementation of clinical processes, procedures, and programs. Additionally, Clinical Research Manager may require a master's degree in nursing. May require ACRP or SOCRA Clinical Research Professional exam completion. Typically reports to a director. The Clinical Research Manager manages subordinate staff in the day-to-day performance of their jobs. True first level manager. Ensures that project/department milestones/goals are met and adhering to approved budgets. Has full authority for personnel actions. To be a Clinical Research Manager typically requires 5 years experience in the related area as an individual contributor. 1-3 years supervisory experience may be required. Extensive knowledge of the function and department processes. (Copyright 2024 Salary.com)
Recently Added Clinical Research Manager jobs
Clinical Research Coordinator
- Innovo Research
-
New Britain, CT
FULL_TIME
-
Job Summary
A Research Coordinator is responsible for reviewing, processing, and managing clinical research data and documents, both regulatory and patient records. The CRC performs a variety of clinical procedures, and assists with daily workload planning; ie; collect, record, report, and interpret data on patients enrolled in and/or seeking enrollment in clinical studies according to the protocol, SOPs and GCPs.
Essential Duties/Responsibilities- Provide clinical research support to investigators to prepare for and execute assigned research studies, including:
- Collect, record, and maintain research subject study data according to study protocols and SOPs, preserving quality control for content, accuracy, and completeness.
- Collect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies governing the conduct of clinical research.
- Recruit and screen participants for clinical trials and maintain subject screening logs.
- Assist in the initial and ongoing consent process; orient research subjects to the study, including the purpose of the study, procedures, and research process.
- Maintain source documentation based on protocol requirements.
- Schedule and execute study visits and perform study procedures.
- Handle lab testing and analysis, including preparation of specimen collection tubes, shipment, and lab logistics.
- Monitor subject safety and report adverse events/reactions to the Principal Investigator and/or appropriate medical personnel.
- Correspond with research subjects and troubleshoot study-related questions or issues.
- Participate in “huddles” to confirm daily study tasks are assigned to team members and are executed to the expected standards.
- Assist with study data quality checking and query resolution.
- Perform a variety of complex clinical research procedures including but not limited to ECG, sample collection, spirometry, vital signs, dose verification, cannulation, and cardiac telemetry monitoring, if needed.
- Assist investigator in verifying that research study objectives are met on time, within budget and according to applicable protocol requirements, clinical research regulations and quality standards.
- Provide training to new investigator site staff members on study-specific topics and requirements. Assist in maintaining adherence to investigator site staff training requirements by auditing and maintaining training records.
- Prepare for and attend study monitoring visits, study audits, and regulatory inspections with clinical research regulatory agencies.
- Assist research site with coverage planning related to staffing and scheduling for research studies.
- Performs other duties and projects as assigned.
- Bachelor's degree in a related field
- 1-2 years’ Clinical research experience
- Relevant work experience in a clinical environment or medical setting, e.g., medical assistant, assistant nurse, laboratory technician; or equivalent combination of education, training, and experience
- Spanish speaking
- Proficient in the use of Microsoft Office applications
- Understanding of medical terminology
- Strong organizational skills
- Working knowledge of clinical trials
- Knowledge and ability to apply GCP/ICH and all applicable FDA regulations and guidelines for human subject protection, drug, and device.
- In-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
- Skilled in carrying out required clinical procedures such as phlebotomy and vital signs.
- Strong written and verbal communication skills including good command of the English language.
- Excellent organizational and problem-solving skills.
- Effective time management skills with the ability to multi-task and manage competing priorities with exceptional attention to details.
- Ability to establish and maintain effective working relationships with physicians, coworkers, managers, and clients.
- Practice a high level of integrity, honesty, and in maintaining confidentiality.
- 6 Days Ago
Manager, Research Operations
- Multiple Myeloma Research Foundation - MMRF
-
Norwalk, CT
FULL_TIME
- MMRF OVERVIEW:The Multiple Myeloma Research Foundation (MMRF) is the largest nonprofit in the world solely focused on accelerating a cure for each and every multiple myeloma patient. We drive the deve...
- 6 Days Ago
Nurse Manager Clinical Informatics
- Clinical Management Consultants
-
Bridgeport, CT
FULL_TIME
- A leading acute care hospital located in southern Connecticut is now seeking an experienced Nurse Manager Clinical Informatics to join their award winning healthcare team.This organization is recogniz...
- 6 Days Ago
Nurse Manager Clinical Informatics
- Clinical Management Consultants
-
Norwalk, CT
FULL_TIME
- A leading acute care hospital located in southern Connecticut is now seeking an experienced Nurse Manager Clinical Informatics to join their award winning healthcare team. This organization is recogni...
- 8 Days Ago
PACU Clinical Manager RN
- Clinical Management Consultants
-
Hartford, CT
FULL_TIME
- A highly regarded 150 bed hospital located near Hartford, Connecticut, is seeking an experienced and dedicated PACU Clinical Manager RN to lead their Post-Anesthesia Care Unit. The PACU Clinical Manag...
- 17 Days Ago
Clinical Research Assistant - Clinical Research Center
- Hartford Hospital
-
Hartford, CT
FULL_TIME
- Description Job Schedule: Full Time Standard Hours: 40 Job Shift: Shift 1 Shift Details: Flexibility required Work where every moment matters. Every day, almost 30,000 Hartford HealthCare employees co...
- 4 Days Ago
Clinical Research Manager jobs at Popular Companies
Clinical Research Manager
- SQRL
-
San Antonio, TX
- Highlights $75,000 - $80,000 salary Full benefits including: Health, Dental, Vision, 15 days PTO, and 401k with 4%match ...
- 6/12/2024 12:00:00 AM
Clinical Research Manager
- Houston Journal of Health Law & Policy
-
Houston, TX
- Description Oversees investigator-initiated and sponsored clinical research projects. Manages graduate students, post-do...
- 6/12/2024 12:00:00 AM
Clinical Research Manager
- Colgate-Palmolive
-
Piscataway, NJ
- No Relocation Assistance Offered # 159181 - Piscataway, New Jersey, United States **Who We Are** Colgate-Palmolive Compa...
- 6/11/2024 12:00:00 AM
Clinical Research Manager
- Alphatec Spine
-
Carlsbad, CA
- An ATEC Clinical Research Manager (CRM) supports the company's Clinical Research initiatives by managing the clinical re...
- 6/11/2024 12:00:00 AM
Clinical Research Manager
- ENT & Allergy Partners
-
Charleston, SC
- We are an eclectic team inspired by intellectual curiosity and a passion for exceptional patient care. Here we lead with...
- 6/9/2024 12:00:00 AM
Clinical Research Manager
- Texas Oncology
-
Austin, TX
- Overview: Texas Oncology is looking for a full-time Clinical Research Manager to join our team! This position will suppo...
- 6/9/2024 12:00:00 AM
Clinical Research Manager
- Triton Medical Robotics
-
Burlingame, CA
- Triton Medical Robotics, a division of Neptune Medical, is an innovative, venture capital funded medical device startup ...
- 6/9/2024 12:00:00 AM
Clinical Research Manager
- SQRL
-
Winter Park, FL
- Highlights $70,000 - $80,000 salary + up to 10% bonus! Full Benefits and Consistent M-F schedule Fast growing company wi...
- 6/8/2024 12:00:00 AM
About Connecticut
Connecticut is bordered on the south by Long Island Sound, on the west by New York, on the north by Massachusetts, and on the east by Rhode Island. The state capital and fourth largest city is Hartford, and other major cities and towns (by population) include Bridgeport, New Haven, Stamford, Waterbury, Norwalk, Danbury, New Britain, Greenwich, and Bristol. Connecticut is slightly larger than the country of Montenegro. There are 169 incorporated towns in Connecticut.The highest peak in Connecticut is Bear Mountain in Salisbury in the northwest corner of the state. The highest point is just east...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Clinical Research Manager jobs
$107,127 to $141,928
Most Popular Cities in Connecticut for Clinical Research Manager Jobs
What does a Clinical Research Manager do?
Clinical Research Manager in Richland, WA
Clinical research managers must plan every phase of research programs, from initial concept through product development and clinical trials to submission for approval by the U.S.
November 27, 2019
Clinical Research Manager in Spartanburg, SC
Research is both the foundation and the future of medicine.
December 17, 2019
Clinical Research Manager in Vallejo, CA
When transitioning into the clinical research field from a science background, it is good to know what experience you have, what positions you are interested in, and what careers are most appropriate for your background.
December 19, 2019