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Program Manager Research Operations Jobs in DeLand, FL

Easterseals Florida

Operations Manager

Daytona Beach, FL · On-site

$48K - $50K/yr

... Operations Manager to provide on-site leadership and operational support for our Dunn Avenue ... This role ensures the smooth day-to-day functioning of clinical programs while delivering an ...

CVS Health

Operations Manager

Altamonte Springs, FL · On-site

$18 - $28/hr

Customer service leadership Unlike the Store Manager in Training position, the Operations Manager position is not part of the CVS/pharmacy Retail Management Development Program. Operations Managers ...

Crunch Fitness

Operations Manager

Daytona Beach, FL · On-site

$15/hr

The Operations Manager (OM) will assist with the delivery of an amazing Crunch Member Experience ... Support company programs and promotions to help generate new sales leads for optimum new membership ...

Cnx

Operations Manager (Onsite)

Lake Mary, FL · On-site

Operations Manager (Onsite) Join a world-class team in Lake Mary, Fl, as an Operations Manager! The ... Ensures program has proficient training, staff development, and effective employee relation ...

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All JobsProgram Research Operations JobsProgram Manager Research Operations JobsProgram Manager Research Operations Jobs in DeLand, FL

Program Manager Research Operations information

See DeLand, FL salary details

$35.6K

$97.5K

$141.1K

How much do program manager research operations jobs pay per year?

As of Sep 7, 2026, the average yearly pay for program manager research operations in DeLand, FL is $97,472.00, according to ZipRecruiter salary data. Most workers in this role earn between $76,100.00 and $118,000.00 per year, depending on experience, location, and employer.

What is a program manager research operations?

Program Manager Research Operations are professionals who oversee and coordinate the administrative and operational aspects of research programs within organizations such as universities, corporations, or healthcare institutions. Their responsibilities typically include managing budgets, ensuring compliance with regulations, supporting research teams, and improving efficiency in research processes. They act as a bridge between researchers, administrative staff, and external partners to ensure projects run smoothly and meet organizational goals. Program Managers in Research Operations play a critical role in enabling scientific and academic research by providing strategic and logistical support.

What are the main challenges program managers in research operations typically face when coordinating cross-functional teams?

Program Managers in Research Operations often encounter challenges related to aligning diverse stakeholders, balancing multiple project timelines, and ensuring smooth communication between research, product, and operations teams. Successfully navigating these challenges requires strong organizational skills, adaptability, and the ability to manage competing priorities while maintaining research quality and compliance. Regularly facilitating meetings, setting clear expectations, and using project management tools help mitigate these challenges and ensure collaborative progress.

What are the key skills and qualifications needed to thrive as a program manager research operations, and why are they important?

To thrive as a Program Manager Research Operations, you need expertise in research administration, project management, and budget oversight, often supported by a relevant degree and experience in research environments. Familiarity with project management tools (e.g., Asana, MS Project), research compliance systems, and grant management platforms is typically essential. Strong leadership, organizational skills, and effective communication enable collaboration across multidisciplinary teams and stakeholders. These skills ensure efficient research operations, regulatory compliance, and successful project outcomes.

What is the difference between Program Manager Research Operations vs Research Coordinator?

AspectProgram Manager Research OperationsResearch Coordinator
CredentialsBachelor's or higher in related field, project management certifications often preferredBachelor's degree in a relevant field, research experience
Work EnvironmentOversees multiple projects, collaborates with teams, manages budgetsSupports research projects, handles data collection, assists with study logistics
Employer & IndustryResearch institutions, biotech, pharma, academiaResearch labs, clinical settings, academic institutions
Search & Comparison IntentUnderstanding managerial roles in research operationsDetails on research support roles and coordination tasks

The Program Manager Research Operations typically oversees multiple research projects, manages teams, and handles budgets, requiring project management skills. In contrast, a Research Coordinator focuses on supporting specific research studies, managing data collection, and logistical tasks. Both roles are essential in research environments but differ in scope and responsibilities.

What job categories do people searching Program Manager Research Operations jobs in DeLand, FL look for?

The top searched job categories for Program Manager Research Operations jobs in DeLand, FL are:

What cities near DeLand, FL are hiring for Program Manager Research Operations jobs?

Cities near DeLand, FL with the most Program Manager Research Operations job openings:

Program Manager Research Operations jobs near you

Experienced Clinical Research Coordinator (In Person)

Hillcrest Medical Research, LLC

Deland, FL • On-site

$52 - $72/hr

Other

Re-posted 7 days ago

Job description

Position Overview

Hillcrest Medical Research (HMR) is seeking an experienced Clinical Research Coordinator (CRC) to join our clinical team. In this role, you will support daily operations and overall company goals while serving as a key point of contact for patients throughout clinical studies.

As an integral member of the HMR research site team, you will be responsible for planning, coordinating, and executing clinical trials in accordance with study protocols, sponsor and CRO requirements, HMR SOPs, and applicable regulatory guidelines. You will also play a vital role in maintaining strong patient relationships and contributing to the growth of the HMR network.

Key Responsibilities
  • Serve as the primary patient/subject interface, ensuring high-quality data collection in compliance with protocols and regulatory standards
  • Assist with pre-screening, screening, and enrollment of study participants
  • Support and guide subjects throughout clinical trials to ensure a positive experience
  • Develop and support recruitment and contingency plans for each study
  • Perform protocol-required procedures, including:
    • Vital signs
    • Phlebotomy
    • Diagnostic testing
    • Investigational product dispensing
    • Scheduling and visit coordination
    • Drug accountability and reconciliation
    • General organizational tasks (as delegated by the investigator)
  • Accurately complete source documentation and case report forms (paper and electronic)
  • Assist investigators with reporting adverse events (AEs) and serious adverse events (SAEs) in accordance with regulatory requirements
  • Participate in investigator meetings, monitoring visits, audits, seminars, and regional/national meetings
  • Support clinical and operational collaboration across HMR research sites
  • Complete all required HMR SOP training modules in a timely manner
  • Ensure study and visit preparedness, including monitor visit preparation
  • Assist with patient scheduling and recruitment as needed
  • Follow direction and incorporate feedback from supervisors in alignment with HMR policies and procedures
Qualifications & Skills
  • Strong knowledge of medical terminology
  • Solid understanding of ICH/GCP guidelines and regulatory requirements
  • Ability to work independently and as part of a team in a fast-paced environment
  • Excellent interpersonal, communication, and organizational skills
  • Strong ability to prioritize tasks and manage multiple responsibilities
  • High level of attention to detail and accuracy
  • Ability to maintain confidentiality
  • Strong analytical, research, and data management skillsProficiency in Microsoft Office Suite
Education & Experience
  • MA, LPN, RN, CNA, EMT, Paramedic, or equivalent (or higher) preferred
  • Phlebotomy Certification preferred
  • Minimum of 2 years of experience as a Clinical Research Coordinator
Equal Opportunity Statement

Hillcrest Medical Research is an equal opportunity employer. Decisions of employment are made based on business needs, job requirements and applicant’s qualifications without regard to race, color, religion, gender, national origin, disability status, protected veteran status, genetic information and testing, family and medical leave, sexual orientation, gender identity or expression or any other status protected by law. Hillcrest Medical Research is a drug-free work place and all offers of employment are contingent upon passing a pre-employment drug screen.

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