Top 47 R&d manager Jobs in Frederick, Md

Senior Human Subjects Protection Scientist
General Dynamics Information Technology —Fort Detrick, MD
- $85,093 - $101,200 a year
- Hybrid work
- Writing skills
- Office
- 3 years
- Paid time off
- 401(k) matching
Scientist
Meso Scale Diagnostics, LLC. —Gaithersburg, MD
- $101,400 - $154,700 a year
- Microsoft Excel
- Microsoft Outlook
- Public speaking
- Paid parental leave
- AD&D insurance
Quick Apply
Research Associate II / Senior Research Associate
Theradaptive —Frederick, MD
- $84,000 - $105,000 a year
- Full-time
- Mid-level
- Math
- Bachelor's degree
Content Delivery Manager
AstraZeneca —Gaithersburg, MD
- $151,081.60 - $226,622.40 a year
- Overtime
- 7 years
- Office
- High school diploma or GED
- Paid holidays
- Health insurance
4h
Associate Director, Clinical Outcomes Assessment - Quantitative Research - Digital Health R&D Oncology – Evinova
AstraZeneca —Gaithersburg, MD
- $151,227.20 - $226,840.80 a year
- Hybrid work
- Office
- Master's degree
- Bachelor's degree
- Health insurance
- Dental insurance
Senior Manager, Clinical Data Standards
Immunocore —Gaithersburg, MD
- $121,500 - $202,500 a year
- Full-time
- Computer Science
- Master's degree
- SQL
IT PROJECT MANAGER
NCC Corporation —Rockville, MD
- Senior level
- 10 years
R & D Project Manager
Inventwood —Frederick, MD
- English
- Mid-level
- 3 years
Quick Apply
3d
Project Manager III
Katalyst Healthcares & Life Sciences —Walkersville, MD
- Contract
- Training & development
- Senior level
- Commercial
Quick Apply
Manager, Quality Assurance GCP
Immunocore —Gaithersburg, MD
- $107,250 - $178,750 a year
- Full-time
- Microsoft Excel
- Microsoft Outlook
- 5 years
Regulatory Risk & Quality Manager
CICONIX, LLC —Fort Detrick, MD
- Full-time
- Background check
- Office
- Organizational skills
- 401(k)
- Paid time off
Quick Apply
Senior Manager, Clinical Supply Chain Program Lead
Immunocore —Gaithersburg, MD
- $121,500 - $202,500 a year
- Full-time
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
Procurement Manager
Immunocore —Gaithersburg, MD
- Full-time
- Microsoft Excel
- Office
- Senior level
Clinical Compliance/Inspection Readiness, Manager - Clinical Operations
Immunocore —Gaithersburg, MD
- $107,250 - $178,750 a year
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Bachelor of Science
Senior Technical Product Manager
CICONIX, LLC —Fort Detrick, MD
- Full-time
- Background check
- Continuous improvement
- Mentoring
- 401(k)
- Paid time off
Quick Apply
Senior Manager, Medical/Regulatory Writer
Immunocore —Gaithersburg, MD
- $158,000 - $185,000 a year
- Full-time
- Remote
- Microsoft Word
- Management
- Bachelor of Science
5G Tactical OTM Product Manager
Thales —Clarksburg, MD
- $150,300 - $192,050 a year
- Call employer
- Hybrid work
- Engineering
- Office
- 8 years
- Paid parental leave
- Paid holidays
Director of Regulatory Affairs,Tactical and Implementation
Immunocore —Gaithersburg, MD
- $157,500 - $262,500 a year
- Full-time
- 5 years
- Bachelor of Science
- Office
R & D Data Analyst
Inventwood —Frederick, MD
- Bachelor of Science
- Writing skills
- English
Quick Apply
3d
Product Manager
GeneCopoeia —Rockville, MD
- Email
- Mid-level
- Analysis skills
- Doctor of Philosophy

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r&d manager jobs near frederick, md

Senior Human Subjects Protection Scientist

General Dynamics Information Technology -
Fort Detrick, MD

Apply Now

Job Details

$85,093 - $101,200 a year

Benefits

Internal mobility program
Paid time off
401(k) matching

Qualifications

Research ethical considerations
Bachelor's degree
Research regulatory compliance
Productivity software
IRB compliance
FDA regulations

Full Job Description

Your Impact

Own your opportunity to work alongside federal civilian agencies. Make an impact by providing services that help the government ensure the well being and support of U.S. citizens.

Job Description

Seize your opportunity to make a personal impact as a Senior Human Subjects Protection Scientist supporting the Office of Research and Regulatory Compliance (ORRC), Office of Human Research Oversight (OHRO) at Defense Health Agency Research & Development (DHA R&D).

The ORRC OHRO is responsible for ensuring that DHA conducted, contracted, sponsored, supported or managed research, and U.S. Army Medical Command investigations involving human subjects, human anatomical substances or animals are conducted in accordance with Federal, DoD, and international regulatory requirements.

HOW YOU WILL MAKE AN IMPACT:

Provide regulatory-based written review of protocols using standardized checklists to ensure compliance with all applicable Federal, DoD, Food and Drug Administration (FDA), state, host nation, and DHA R&D human subjects protection requirements
This position is tasked with reviewing research protocols that have undergone review and approval by the local Institutional Review Board (IRB); the OHRO reviewer will delineate deficiencies and areas of regulatory noncompliance and make recommendations to the OHRO Federal Approval Authority (AAs) regarding regulatory and ethical issues in OHRO submissions. The reviewer will work with the investigator to make updates/revisions to the materials to bring the protocol into compliance for OHRO approval
Reviewers will be assigned a portfolio of protocols for initial review; this includes determinations of not research, research not involving human subjects, exempt research, non-exempt research, and protocols utilizing cadavers/cadaveric specimens
Provide accurate information, assistance, and documents to customers and OHRO Federal personnel when requested with appropriate professionalism in a timely manner
This will require active management of the assigned protocol portfolio; this includes data entry activities and use of OHRO specific information management systems to track information and activities related to protocol review
Assist the Government to develop policies, procedures, guidelines, and other materials to ensure compliance with current regulations and to update investigators, research managers and administrators, and administrative staff on human subjects protection and regulatory compliance policies and procedures as they apply to research supported by the DHA R&D
Assist in the development of local procedures and guidance for the OHRO and the DHA R&D in the area of human subjects’ protection
Support the development and implementation of effective mechanisms to communicate and interpret these regulations, policies, and guidelines
Assist in development and implementation of internal OHRO operating procedures and review guidelines as requested
Foster regulatory compliance through education and training of investigators, research managers, administrators, and OHRO staff, and provide assistance to program offices and investigators with interpretation of human subjects protection and cadaver use requirements
Acquire and retain knowledge of current Federal, DoD, FDA, Army, state, host nation, and DHA regulatory requirements related to the protection of human subjects in research and cadaver use and apply knowledge of these regulations and general ethical principles during OHRO reviews of assigned projects
Interact with colleagues, consultants, investigators, research directors, supervisors, other US Army personnel, etc., to gather or disseminate information or to provide assistance related to assigned protocols, attend meetings and conference calls as necessary, and provide education on human subjects protection regulations and OHRO requirements
Participate in performance improvement activities and shall task contract personnel to participate in specific working groups to improve and streamline the protocol review and approvals processes, and provide input and assistance with formulating and writing OHRO standard operating procedures and work instructions

WHAT YOU’LL NEED TO SUCCEED:

Education: Bachelor’s Degree in a scientific, or related discipline
Required Experience: 3+ years of related human subjects’ protection experience
Required Technical Skills: Knowledge of the Federal regulations governing the protection of human research subjects, including a firm foundation in the Common Rule and FDA regulations, to allow for effective and responsible management of a caseload of research protocols submitted for DHA R&D review and oversight; Working knowledge of ethical principles related to participation of humans in research; Working knowledge of scientific research concepts and terminology to properly conduct detailed analyses of all research protocols submitted for IRB review; Following individual training and guidance, ability to become expert at applying DoD, and DHA R&D human subjects protection regulations, policies and guidelines; Proficiency with Microsoft Office Suite
Attributes for Success: Ability to effectively communicate with researchers, research staff, and IRB members on matters of research compliance and ethical human research practices; Possess excellent organizational skills and
professional conduct and businesslike manner, meticulous attention to detail, committed to helping build and sustain team success; Ability to track multiple tasks and review actions; excellent critical thinking and problem solving skills
Preferred Skills: 5 + years experience; Ability to become proficient in the use of an electronic document management system
Location: Ft Detrick (Frederick, Maryland) Hybrid schedule (work 1 day onsite and remainder remote)
Work Hours: Staff are expected to be accessible during core hours of 9AM to 3PM, but have flexibility to set their schedule around those core hours
US citizenship required
Security Clearance: Clearable for a NACI (T1) security investigation

GDIT IS YOUR PLACE:

At GDIT, the mission is our purpose, and our people are at the center of everything we do.

Growth: AI-powered career tool that identifies career steps and learning opportunities
Support: An internal mobility team focused on helping you achieve your career goals
Rewards: Comprehensive benefits and wellness packages, 401K with company match, and competitive pay and paid time off
Community: Award-winning culture of innovation and a military-friendly workplace

#GDITFedHealthJobs

#GDITHealth

Work Requirements

Years of Experience

5 + years of related experience

may vary based on technical training, certification(s), or degree

Certification

Travel Required

10-25%

Citizenship

U.S. Citizenship Required

Salary and Benefit Information

The likely salary range for this position is $85,093 - $101,200. This is not, however, a guarantee of compensation or salary. Rather, salary will be set based on experience, geographic location and possibly contractual requirements and could fall outside of this range.
View information about benefits and our total rewards program.

Our Identity Verification Process

As part of the hiring process, we will ask you to complete an identity verification process that leverages advanced biometrics and artificial intelligence to ensure authenticity and protect against identity fraud. You are expected to be on camera during virtual interviews. We reserve the right to take your picture to verify your identity and prevent fraud. By proceeding, you authorize the collection, processing, and use of your biometric data for identity verification and security purposes.

About Our Work

We are GDIT. A global technology and professional services company that delivers technology solutions and mission services to every major agency across the U.S. government, defense and intelligence community. Our 26,000 experts extract the power of technology to create immediate value and deliver solutions at the edge of innovation. We operate across 50+ countries worldwide, offering leading mission-ready capabilities in AI, cloud, cyber and software development.

Join our Talent Community to stay up to date on our career opportunities and events at gdit.com/tc.

Equal Opportunity Employer / Individuals with Disabilities / Protected Veterans

Apply Now

Refine Your Search

r&d manager jobs in frederick, md

Senior Human Subjects Protection Scientist

Scientist

Research Associate II / Senior Research Associate

Content Delivery Manager

Associate Director, Clinical Outcomes Assessment - Quantitative Research - Digital Health R&D Oncology – Evinova

Senior Manager, Clinical Data Standards

IT PROJECT MANAGER

R & D Project Manager

Project Manager III

Manager, Quality Assurance GCP

Regulatory Risk & Quality Manager

Senior Manager, Clinical Supply Chain Program Lead

Procurement Manager

Clinical Compliance/Inspection Readiness, Manager - Clinical Operations

Senior Technical Product Manager

Senior Manager, Medical/Regulatory Writer

5G Tactical OTM Product Manager

Director of Regulatory Affairs,Tactical and Implementation

R & D Data Analyst

Product Manager

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