Northwestern University

Clinical Research Project Manager

Northwestern University$82K — $86K *
Healthcare
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's or higher degree in social or health science or related field, or equivalent combination of education and experience with 5+ years in research studies
  • Master's degree in social or health science or related field, or equivalent combination with 3+ years in research studies
  • Proven supervisory or project management experience
  • CITI training completion required before participant interaction, with re-certification every 3 years
  • Strong attention to detail and ability to oversee complex, multi-faceted research operations

Responsibilities

  • Manage complex biomedical and social-behavioral research studies
  • Ensure compliance with Good Clinical Practices and regulations
  • Oversee day-to-day operations and resource allocation
  • Facilitate meetings and monitor project timelines
  • Co-author scientific papers and coordinate grant submissions

Benefits

  • Flexible work environment with opportunities for interdisciplinary collaboration
  • Professional development through training and mentorship
  • Involvement in leading-edge research on early interventions for children
  • Access to a variety of resources for conducting high-quality research
  • Engagement with community partners in impactful research initiatives
Full Job Description
Department: SoC Comm Sciences & Disorders
Salary/Grade: EXS/7

Target hiring range for this position will be between $82,000-$86,000 per year. Offered salary will be determined by the applicant's education, experience, knowledge, skills and abilities, as well as internal equity and alignment with market data.

Job Summary

Manages all activities associated with biomedical &/or social-behavioral research studies considered very complex by the inclusion of several of the following: multiple investigators, teams, sites, sub-contracts, participants, longitudinal assessments/ interventions; &/or multi-million dollar budgets. Ensures completion of contract requirements & client specifications. Oversees day-to-day operations including identifying & securing needed resources; creating, implementing, monitoring, & updating project plans; facilitating meetings with appropriate parties; tracking tasks/deliverables to ensure timelines, milestones &/or goals are attained; monitoring & reporting progress as appropriate; & resolving or escalating issues in a timely manner. May co-author scientific papers for presentation & publication & coordinates writing, submission & administration of grants. Ensures that all study activities are completed by strictly following Good Clinical Practices (GCP) & all current local, state, & federal laws, regulations, guidance, policy & procedure developed by the NU Institutional Review Board (IRB), Food & Drug Administration (FDA) Code of Federal Regulations (CFR), & the International Conference on Harmonization (ICH).

The Early Intervention Research Group (EIRG) is led by Dr. Megan Roberts. This lab examines the effects of early intervention for children with developmental delays (6 months to 4 years). The EIRG uses a variety of methodologies including clinical trials, behavioral observations, and surveys. Data is longitudinal with multiple measures at each time point. Because the EIRG blends research and clinical practice, this position requires a flexible and creative thinker who can work as part of an interdisciplinary team.

This position requires someone with a strong attention to detail who can also consider the big picture and has many years of experience with operations and management. The position includes managing the work of several subcontracts and conducting supervising several temporary employees to implement clinical interventions and assessments for a research study. Additionally, the position includes conducting standardized assessments, delivering evidenced-based language interventions to children and their caregivers, and coordination with community partners, and additional research tasks, such as coding data and entering/verifying data. We are also looking for a team player who prefers open and honest communication and is willing to take initiative and learn a variety of lab related responsibilities, including larger tasks like helping to a launch new research grants and small tasks like data entry, data quality checks, scoring assessments, and transcribing and coding parent/child interactions or therapist/child/parent interactions.

Principal Accountabilities

Technical
  • Provides complex scientific & technical leadership in determining research priorities & the plan, design & execution of research projects ensuring that programs of investigation meet specified objectives.
  • Plans, develops & implements new processes & protocols to support research studies & maximize/extend study capabilities.
  • Oversees completion of study activities per protocol. Collaborating with nursing staff and Principal Investigator (PI) ascertains pretreatment & eligibility requirements; interviews participants & obtains social & medical his
  • tories; based on results determines & registers participants with appropriate sponsors; completes informed consent; determines & organizes patient's treatment and test schedules.
  • Ensures that study protocols are in compliance with appropriate rules & regulations & reviews study progress and recommends revisions, amendments, and/or other study changes as necessary to better meet needs of sponsors. Manages conduct of experimental tests & procedures. Closely monitors & documents patient's adverse events; partners with nursing staff in modifying dosages, tests & treatment schedule.
  • Reviews scientific literature & evaluates & recommends applicable techniques & procedures.
Administrative
  • Analyzes, evaluates & interprets data to determine relevance to research.
  • Assists PI in developing statistical methods & models to analyze & report data based upon study requirements.
  • Prepares results & may co-author scientific papers for presentation & publication & disseminates information via seminars, lectures, etc.
    Creates data for use in grant submission & develop new proposals for research including obtaining financial support.
  • Acts as liaison between sponsoring agencies, collaborating organizations &/or other research &/or educational institutions.
  • Ensures that all study documents associated with current local, state, & federal regulatory guidelines, requirements, laws & research protocols are completed in a timely manner.
    Data
  • Manages project data including processing, accuracy, analysis & evaluation of data ensuring that results meet project information and deliverable objectives. Partners with internal/external project and IT staff to create, review, analyze, interpret, summarize and prepare progress & final reports.
  • Provides consultation to internal/external project staff on appropriate data management, methodological issues and analysis of data.
Finance
  • May create &/or manage research study budget which may include deciding on & approving expenditures of funds based on budget.
  • Monitors accounts.
  • Negotiates prices & specifications with vendors.
  • Purchases supplies, materials, equipment & services.
  • Ensures appropriate allocation & compliance.
  • Invoices study sponsors for study tests/procedures.
  • Coordinates & participates in budgetary negotiations with industry sponsors.
Supervision
  • Trains, directs, assigns duties to & may supervise lab EEs, students, residents &/or fellows.
  • Acts as a mentor in regard to education of junior coordinators.
  • Performs other duties as assigned.
Minimum Qualifications: (Education, experience, and any other certifications or clearances)
  • Successful completion of a full 4-year course of study in an accredited college or university leading to a bachelor's or higher degree in a major such as social or health science or related; OR appropriate combination of education and experience and 5 years' research study or other relevant experience required; OR
  • Successful completion of a full course of study in an accredited college or university leading to a master's or higher degree in a major such as social or health science or related; OR appropriate combination of education and experience and 3 years' research study or other relevant experience.
  • Supervisory or project management experience required.
  • Must complete NU's IRB CITI training before interacting with any participants & must re-certify every 3 years.

About Northwestern University

Northwestern University is a private research university in Evanston, Illinois. It was founded in 1851 by nine men whose goal was to establish a university that would serve the Northwest Territory. Northwestern is a member of the Big Ten Conference and the Association of American Universities. Northwestern has 12 undergraduate, graduate, and professional schools offering 124 undergraduate degrees and 145 graduate and professional degrees. Northwestern has a diverse student body with over 21,000 students from all 50 states and 100 countries. The university has a strong focus on research and has produced 19 Nobel laureates, as well as numerous Pulitzer Prize and MacArthur Fellowship winners.
Learn more about Northwestern University
Size
1,483 employees
Market Cap
$3.3 billion
Industry
Net Income
$155.2 million
5 Year Trend
+1.8%
Revenue
$1.1 billion
NASDAQ

Similar Jobs

More Jobs at Northwestern University

More Healthcare Jobs

Find similar Clinical Research Project Manager jobs: