Market Research Supervisor jobs in New Hampshire

Market Research Supervisor supervises activities in the market research department. Ensures appropriate use of analytic techniques to determine demand for products and services. Being a Market Research Supervisor interprets and predicts consumer trends, formulates research and development proposals, and monitors research projects. A level I supervisor is considered a working supervisor with little authority for personnel actions. Additionally, Market Research Supervisor may require a bachelor's degree in area of specialty. Typically reports to a manager or head of a unit/department. Working team member that may validate or coordinate the work of others on a support team. Suggests improvements to process, is a knowledge resource for other team members. Has no authority for staff actions. Generally has a minimum of 2 years experience as an individual contributor. Thorough knowledge of the team processes. (Copyright 2024 Salary.com)

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Clinical Research Coordinator
  • Alcanza Clinical Research
  • Portsmouth, NH FULL_TIME
  • Department: Operations

    Employment Type: Full Time

    Location: ActivMed Practices & Research | Portsmouth, NH

    Reporting To: Christopher Lenox

    Description

    Alcanza is a growing multi-site, multi-phase clinical research company with a network of locations in MA, NH, MI, VA, SC, FL, GA, AL, MO, TX and Puerto Rico. We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow.

    We have established a strong presence across Phase I-IV studies and several therapeutic areas including vaccine, neurology, dermatology, psychiatry, and general medicine. Join us as we continue to grow, the Clinical Research Coordinator under the direction of the Site Manager/Director and the Principal/Sub Investigators conducts the following according to the study protocol, company processes & procedures, and in compliance with FDA, GCP, and ICH regulations and guidelines. The Clinical Research Coordinator (CRC) works to ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations, and SOPs.

    Key Responsibilities

    In collaboration with other members of the clinical research site team works to ensure the execution of assigned studies. Responsibilities may include but are not limited to:

    Under The Direction Of The Site Manager/Director And The Principal/Sub Investigators, Conducts The Following According To Study Protocol, Company Processes & Procedures, And In Compliance With FDA, GCP, ICH Regulations And Guidelines

    • Screening of patients for study enrollment;
    • Patient consents;
    • Patient follow-up visits;
    • Documenting in source clinic charts;
    • Entering data in EDC and answers queries;
    • Obtaining vital signs and ECGs;
    • May perform basic lab procedures per protocol, such as: blood specimen collection, centrifuge operation, storing and shipping of lab specimens, accountability of specimens and notification of courier for specimen pick-up;
    • Requesting and tracking medical record requests;
    • Updating and maintaining logs, chart filings;
    • Maintaining & ordering study specific supplies;
    • Scheduling subjects for study visits and conducts appointment reminders;
    • Building/updating source as needed;
    • Conducting monitoring visits and resolves issues as needed in a timely manner;
    • Ensuring study related reports and patient results are reviewed by investigator in a timely manner;
    • Filing SAE/Deviation reports to Sponsor and IRB as needed;
    • Documenting and reporting adverse events;
    • Reporting non-compliance to appropriate staff in timely manner;
    • Maintaining positive and effective communication with clients and team

    members;

    • Always practicing ALCOAC principles with all documentation;
    • Complete all needed activities for study start-up, including completing required training, uploading / printing certificates to file in ISF, etc.;
    • Prepare and attend site initiation visits (SIV's) and Investigator Meetings (IMs), as needed;
    • Handles all IRB functions for assigned studies independently, and/or with assigned regulatory team member, as needed;
    • Assist with training of new research assistants and coordinators;
    • Assist with scheduling and planning for visit capacity for assigned studies;
    • May set up, train and maintain all technology needed for studies;
    • May assist with study recruitment, patient enrollment, and tracking as needed;
    • May handle more complex study assignments and volumes;
    • May participate in community outreach / education events;
    • Maintaining confidentiality of patients, customers and company information, and;
    • Performing all other duties as requested or assigned.

    Skills, Knowledge And Expertise

    Minimum Qualifications: A Medical Assistant diploma, LPN/LVN, EMT credential AND 2 years of clinical research coordination experience, OR an equivalent combination of education and experience, is required. Proficiency with performing basic clinical procedures such as (blood pressure, vitals, EKGs, phlebotomy, etc.) is highly preferred. CCRC or CCRP credential and BLS certification preferred. Bi-lingual (English / Spanish) proficiency is a plus.

    Required Skills

    • Proficiency with computer applications such as Microsoft applications, email, electronic health records, web applications, and the ability to type proficiently (40 wpm);
    • Performing basic clinical procedures such as blood pressure, vitals, EKGs, phlebotomy, etc
    • Strong organizational skills and attention to detail.
    • Well-developed written and verbal communication skills.
    • Well-developed interpersonal and listening skills and the ability to work well independently as well as with co-workers, subjects, managers and external customers.
    • Ability to effectively handle multiple tasks, and adapt to changes in workloads and priorities.
    • Must be professional, respectful of others, self-motivated, and have a strong work ethic.
    • Must possess a high degree of integrity and dependability.
    • Ability to work under minimal supervision, identify problems and implement solutions.
    • Ability to handle highly sensitive information in a confidential and professional manner, and in compliance with HIPAA guidelines.

    Benefits

    • Full-time employees regularly scheduled to work at least 30 hours per week are benefits-eligible, with coverage starting on the first day of the month following date of hire.
    • Medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match are offered.
  • 5 Days Ago

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Clinical Research Assistant / EMT
  • Alcanza Clinical Research
  • Portsmouth, NH FULL_TIME
  • Department: OperationsEmployment Type: Full TimeLocation: ActivMed Practices & Research | Portsmouth, NHReporting To: Christopher LenoxDescriptionAlcanza is a growing multi-site, multi-phase clinical ...
  • 11 Days Ago

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Clinical Research Assistant / Medical Assistant
  • Alcanza Clinical Research
  • Portsmouth, NH FULL_TIME
  • Department: OperationsEmployment Type: Full TimeLocation: ActivMed Practices & Research | Portsmouth, NHReporting To: Christopher LenoxDescriptionAlcanza is a growing multi-site, multi-phase clinical ...
  • 4 Days Ago

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Medical Assistant / Clinical Research Assistant
  • Alcanza Clinical Research
  • Portsmouth, NH FULL_TIME
  • Medical Assistant / Clinical Research AssistantDepartment: Operations Employment Type: Full TimeLocation: ActivMed Practices & Research | Portsmouth, NHReporting To: Christopher LenoxDescriptionAlcanz...
  • 20 Days Ago

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Clinical Research Patient Recruiter (Patient Registrar) - onsite
  • Alcanza Clinical Research
  • Portsmouth, NH FULL_TIME
  • Clinical Research Patient Recruiter (Patient Registrar) - onsiteDepartment: Patient Recruitment Employment Type: Full TimeLocation: ActivMed Practices & Research | Pease, NHDescriptionAlcanza is a gro...
  • 26 Days Ago

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Data entry
  • Maxion Research
  • Portsmouth, NH FULL_TIME
  • Unleash your skillset within an accommodating role that can be managed from any location! Are you searching for a new way to make money? Look no further we are seeking individuals now who can work rem...
  • 5 Days Ago

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Clinical Research Coordinator / Research assistant
  • Drug Trials America
  • Hartsdale, NY
  • Job Description Job Description Position Requirements: *Hard Working *Meticulous/ detail oriented *Good with people *abl...
  • 6/11/2024 12:00:00 AM

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Research Coordinator
  • Harvard University
  • Cambridge, MA
  • At the Developmental Relationships Lab, our goal is to conduct research and develop professional learning materials to s...
  • 6/11/2024 12:00:00 AM

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Clinical Research Coordinator - Research-Other
  • Eisenhower Medical Center
  • Rancho Mirage, CA
  • * Share Job: * Email * Facebook * Linkedin chevron_left Back To Results Located in the heart of the Coachella Valley, yo...
  • 6/10/2024 12:00:00 AM

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Research Coordinator
  • NYU Langone Health
  • New York, NY
  • NYU Grossman School of Medicine is one of the nation's top-ranked medical schools. For 175 years, NYU Grossman School of...
  • 6/10/2024 12:00:00 AM

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Clinical Research Coordinator
  • Sanford Health
  • Fargo, ND
  • Careers With Purpose Sanford Health is one of the largest and fastest-growing not-for-profit health systems in the Unite...
  • 6/10/2024 12:00:00 AM

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Clinical Research Coordinator-Research
  • Nemours Children's Health
  • Wilmington, DE
  • Job Description The Clinical Research Coordinator coordinates, implements and completes clinical research studies and/or...
  • 6/8/2024 12:00:00 AM

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Clinical Research Coordinator - Research Institute
  • Avera Health
  • Pierre, SD
  • Full Time MCK ARI Grant Admin 3900 W Avera Drive Technical/Professional Day Shift Join the team at Avera! Award Winning ...
  • 6/7/2024 12:00:00 AM

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Clinical Research Coordinator (Research Professional 1)
  • University of Minnesota
  • Minneapolis, MN
  • About the Job We are seeking a motivated and detail-oriented Clinical Research Coordinator (Research Professional 1) to ...
  • 6/7/2024 12:00:00 AM

New Hampshire is part of the six-state New England region. It is bounded by Quebec, Canada, to the north and northwest; Maine and the Atlantic Ocean to the east; Massachusetts to the south; and Vermont to the west. New Hampshire's major regions are the Great North Woods, the White Mountains, the Lakes Region, the Seacoast, the Merrimack Valley, the Monadnock Region, and the Dartmouth-Lake Sunapee area. New Hampshire has the shortest ocean coastline of any U.S. coastal state, with a length of 18 miles (29 km), sometimes measured as only 13 miles (21 km). New Hampshire was home to the rock forma...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Market Research Supervisor jobs
$61,555 to $101,139

Market Research Supervisor in Altoona, PA
While market research supervisors have much in common with market research managers, their position is much more “hands on” with the research team.
January 22, 2020
Market Research Supervisor in Springfield, OH
Prior Market Research experience is highly preferred (3 years).
February 09, 2020
Market Research Supervisor in Schenectady, NY
Its core activities are recruiting for qualitative and quantitative research.
January 05, 2020