Scientist - Clinical Research jobs in Connecticut
Scientist - Clinical Research assumes lead role in various clinical research projects. Proposes, plans, organizes and executes experiments and research. Being a Scientist - Clinical Research secures grants and funding for research and is responsible for controlling budgets. Summarizes findings in reports and communicates results. Additionally, Scientist - Clinical Research interacts with other scientists within and outside of the organization. Provides recommendations that influence extensive clinical research activities. Requires an advanced degree. Typically reports to head of a unit/department. The Scientist - Clinical Research work is generally independent and collaborative in nature. Contributes to moderately complex aspects of a project. To be a Scientist - Clinical Research typically requires 4 -7 years of related experience. (Copyright 2024 Salary.com)
Recently Added Scientist - Clinical Research 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.
- 4 Days Ago
Research Scientist
- Nesco Resource
-
New Haven, CT
CONTRACTOR
- ONSITE 5 DAYS, NEW HAVEN ONLY, PARKING WILL BE REIMBURSED.This Is What You Will DoThe position is required to join Injectable Drug Product Development group of *** pharmaceuticals' Analytical and Phar...
- 1 Day Ago
Research Scientist
- Joulé
-
New Haven, CT
CONTRACTOR
- Job Title: Research ScientistLocation: New Haven, CTSchedule / Hours: Monday - Friday, Full timeType: Contract to HireResponsibilitiesRoutine maintenance of plant tissue culture, various speciesMedia ...
- 11 Days Ago
Research Scientist
- Wesleyan University
-
Middletown, CT
FULL_TIME
- The Wave Transport in Complex Systems group at the Physics Department of Wesleyan University has a Research Scientist position available. Under the direction of Dr. Tsampikos Kottos, the Research Scie...
- Just Posted
Associate Scientist - Research Scientist, Neuroscience
- Planet Pharma
-
New Haven, CT
FULL_TIME
- Job DescriptionPosition Summary:This is an exciting opportunity to join our growing Neuroscience team. As client's portfolio of preclinical and clinical programs continues to expand, the candidate for...
- 7 Days Ago
Scientist II (ELISA, QPCR,ASSAY DEVELOPMENT)
- Maxis Clinical Sciences
-
Ridgefield, CT
FULL_TIME
- Job DescriptionJob Title: Scientist IIDuties: Design, plan and execute experiments in a timely and independent manner leveraging scientific and technical expertise to achieve defined objectives. Indep...
- 7 Days Ago
Scientist - Clinical Research jobs at Popular Companies
Principal Scientist, Clinical Research
- J&J Family of Companies
-
Cincinnati, OH
- Principal Scientist, Clinical Research - 2406190642W **Description** Johnson & Johnson, we believe health is everything....
- 6/10/2024 12:00:00 AM
Principal Scientist, Clinical Research, Thoracic Malignancies
- Merck
-
Rahway, NJ
- **Job Description** Our company is a global health care leader with a diversified portfolio of prescription medicines, v...
- 6/9/2024 12:00:00 AM
Principal Scientist, Clinical Research, Thoracic Malignancies
- Merck
-
North Wales, PA
- **Job Description** Our company is a global health care leader with a diversified portfolio of prescription medicines, v...
- 6/9/2024 12:00:00 AM
FEMA - Scientific Specialist (Nationwide Openings)
- Idaho State Job Bank
-
Idaho Falls, ID
- FEMA - Scientific Specialist (Nationwide Openings) at CDM Smith in Idaho Falls, Idaho, United States Job Description 272...
- 6/9/2024 12:00:00 AM
FEMA - Scientific Specialist (Nationwide Openings)
- Idaho State Job Bank
-
Nampa, ID
- FEMA - Scientific Specialist (Nationwide Openings) at CDM Smith in Nampa, Idaho, United States Job Description 27234BR R...
- 6/9/2024 12:00:00 AM
Principal Scientist, Clinical Research, Breast Cancer
- Merck
-
Rahway, NJ
- **Job Description** Our company is a global health care leader with a diversified portfolio of prescription medicines, v...
- 6/8/2024 12:00:00 AM
Senior Scientist
- Meet
-
Ridgefield, CT
- Our esteemed client, a leading top 20 pharmaceutical company known for its continuous growth, is seeking a Senior Scient...
- 6/7/2024 12:00:00 AM
Scientific Director, Clinical Scientist, Oncology Early Development
- AbbVie, Inc.
-
South San Francisco, CA
- In collaboration with a therapeutic area, the Scientific Director, Clinical Science will lead the design, conduct, analy...
- 6/6/2024 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 Scientist - Clinical Research jobs
$90,130 to $128,147
Most Popular Cities in Connecticut for Scientist - Clinical Research Jobs
What does a Scientist - Clinical Research do?
Scientist - Clinical Research in Savannah, GA
Most scientists choose to complete a dual degree, in both science and medicine.
January 10, 2020
Scientist - Clinical Research in Fort Wayne, IN
Natural sciences managers supervise the work of scientists, including chemists, physicists, and biologists.
February 15, 2020
Scientist - Clinical Research in Norwich, CT
Research projects may be aimed at improving manufacturing processes, advancing basic scientific knowledge, or developing new products.
December 15, 2019