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Contract Cardiovascular Research Jobs (NOW HIRING)

Vitalief

Clinical Research Coordinator

Newark, NJ · On-site

$65K - $78K/yr

... cardiovascular research, and the ability to work independently while serving as the primary ... Contracts & Budget Support * Assist with clinical trial agreement (CTA) coordination and budget ...

Vitalief

Clinical Research Coordinator

Newark, NJ · On-site

$65K - $78K/yr

... cardiovascular research, and the ability to work independently while serving as the primary ... Contracts & Budget Support * Assist with clinical trial agreement (CTA) coordination and budget ...

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As of Aug 15, 2026, the average hourly pay for contract cardiovascular research in the United States is $32.74, according to ZipRecruiter salary data. Most workers in this role earn between $21.63 and $39.90 per hour, depending on experience, location, and employer.

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Contract Cardiovascular Research jobs near you

Cardiology Research Manager

Beacon Health System

Elkhart, IN • On-site

Part-time

Posted 10 days ago

Beacon Health System rating

6.7

Company rating: 6.7 out of 10

Based on 143 frontline employees who took The Breakroom Quiz

530th of 887 rated healthcare providers

Job description

Reports to the Group Practice Manager or designee and the Midwest Cardiovascular Research and Education Foundation (MCREF). Plans, coordinates and oversees the operational functions of the clinical research program and MCREF activities to ensure efficient study execution, regulatory compliance, organization of foundation events, financial stewardship, and high-quality service. Serves as the operational liaison among investigators, board members, research staff, sponsors, patients, and internal departments. This position emphasizes research operations, project management, Foundation management, fiscal oversight, and process improvement.
MISSION, VALUES and SERVICE GOALS
  • MISSION: We deliver outstanding care, inspire health, and connect with heart.
  • VALUES: Trust. Respect. Integrity. Compassion.
  • SERVICE GOALS: Personally connect. Keep everyone informed. Be on their team.

Responsibilities
  • Plans, coordinates, and oversees day-to-day administrative operations of the research program.
  • Develops and maintains workflows, standard operating procedures, and operational processes.
  • Coordinates research meetings, agendas, action items, and follow-up.
  • Maintains investigators and research staff calendars and coordinates study-related meetings.
  • Oversees research project budgets, prepares billing, and monitors expenditures working alongside foundation accounting personnel and lead study coordinators.
  • Coordinates research billing activities and collaborates with finance and revenue cycle to ensure compliant research billing.
  • Monitors study financial performance, sponsor milestones, and contract deliverables.
  • Coordinates patient scheduling and follow-up activities to support protocol compliance when needed.
  • Collaborates with investigators, coordinators, sponsors, ancillary departments, and leadership to resolve operational issues.
  • Facilitates conflict resolution among research staff and stakeholders.
  • Assists with the operational metrics, prepares reports, and identifies opportunities for process improvement.
  • Supports onboarding, education, and competency development of research personnel.
  • Coordinates implementation of new studies and operational initiatives.
  • Performs other duties and special projects as assigned.

Leadership Competencies
  • Drives Results
  • Customer Focus
  • Instills Trust
  • Collaborates
  • Communicates Effectively

ORGANIZATIONAL RESPONSIBILITIES
  • Attends department meetings and is accountable for shared information.
  • Completes mandatory education and annual competencies.
  • Maintains required licensure/certification, if applicable.
  • Adheres to regulatory agency requirements and organizational policies.
  • Available to work additional hours when operationally necessary.

Qualifications
  • Bachelor's degree required
  • Three to five years of progressively responsible clinical research or healthcare operations experience preferred
  • Project leadership or supervisory experience preferred

Knowledge & Skills
  • Knowledge of GCP, FDA, IRB, and sponsor requirements.
  • Knowledge of clinical research billing compliance.
  • Strong budgeting, financial management, project management, and organizational skills.
  • Excellent verbal and written communication skills.
  • Ability to manage multiple priorities and resolve conflict.
  • Proficiency with Microsoft Office and clinical research systems.

Working Conditions
  • Office environment with occasional travel between Beacon locations.

Physical Demands
  • Requires the physical ability and stamina to perform the essential functions of the position.

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