Top 2 Executive director/site head Jobs in Frederick, Md

Executive Director/Site Head
Precision Medicine Group —Frederick, MD
- $203,200 - $304,800 a year
- Online Application
- Microsoft Word
- Microsoft Excel
- 11+ years
Executive Director/Site Head
Precision for Medicine —Frederick, MD
- $203,200 - $304,800 a year
- Online Application
- Microsoft Word
- Microsoft Excel
- 11+ years
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Executive Director/Site Head
Precision Medicine Group —Frederick, MD
ISO 13485 and 15189 principles of design control, understanding of both CLIA and CLSI validation requirements, and assay execution of both cell-based and non-…
$203,200 - $304,800 a year

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Executive Director/Site Head

Precision Medicine Group -
Frederick, MD

Apply Now

Job Details

$203,200 - $304,800 a year

Qualifications

Microsoft Word
Customer communication
Microsoft Excel
Presentation software
Team leadership
ISO standards
CAP guidelines
English
Assay development
Clinical laboratory experience
Managing research teams
Managing laboratory teams
Supervising experience
Doctor of Philosophy
CLIA regulations
Regulatory/legal compliance standards in production
Design controls
Biomedical regulatory compliance
Clinical quality assurance standards
Compliance standards auditing
Method validation

Full Job Description

Position Summary:

The Executive Director / Site Head of Precision for Medicine (located onsite in Frederick, MD) will be responsible to oversee the laboratory operations across 3 different functional groups in Frederick, Maryland. This role is responsible for ensuring that lab environments, processes, and systems are optimized to enable scientific and operational excellence while maintain regulatory compliance. A critical requirement is deep current knowledge of FDA guidance documents and requirements, along with the ability to put these requirements into practice developing robust assays that easily pass FDA scrutiny. Experience with developing and managing programs following FDA/IVDR,. ISO 13485 and 15189 principles of design control, understanding of both CLIA and CLSI validation requirements, and assay execution of both cell-based and non-cell-based assays is required.

Essential functions of the job include but are not limited to:

Full responsibility of operational aspects for all laboratories in Frederick MD; including Bioanalysis, Flow Cytometry and Companion Diagnostic.
Support, hire, coach and mentor laboratory lab heads in Bioanalytical, Flow and CDx
Collaborate with site supporting departments: Facilities, Biorepository, Quality Assurance, Finance, as well as other global site heads.
Monitor and report site KPIs including quality events, turnaround time, capacity, revenue delivery and budget adherence.
Is fully responsible for improving operations and enhancing operational excellence in each laboratory.
Responsible for weekly and monthly revenue reporting, cost tracking and margin expansion.
Provide operational excellence leadership ensuring that the team is efficient and has appropriate resourcing.
Mentor and lead laboratory head for all applicable laboratories.
Direct staff to ensure consistent scientific standards and compliance with Precision procedures and regulatory expectations on all projects
Ensure all work is completed to the appropriate regulatory guidelines, CAP/ CLIA/ GxP.. etc..
Work closely with QA and our regulatory team to ensure compliance to industry standards.
Attend and actively participate in FDA calls regarding assay development and compliance.
Ensures all development and validation study protocols and reports meet CAP/CLIA and CLSI requirements
Establish and implement a communication strategy to ensure timely and consistent dissemination of information to engage key stakeholders across the site and within Precision.
Communicate clearly with clients and manage client expectations for all projects within the teams
Is responsible for establishing best practices for company business operations processes and systems to support growth and efficiencies.
Prepare/review critical documents including protocols, reports, and SOPs as applicable: Oversee the establishing and improving of all procedures and required SOP documentation
Oversee the team in relation to trouble shooting and correcting all scientific issues/problems within the teams
Support all leaders in the review of data and provide written and verbal technical updates to clients as needed; be an escalation point for clients.
Work collaboratively with other technical teams in resource sharing and providing technical expertise
Act as a scientific resource externally to clients and internally on Product and Services/ R&D related projects
Assist with writing, reviewing and editing contracts and scope of works, change orders.
Maintain and support safe lab practices and environment
Carry out other duties/projects as assigned

Qualifications:

Minimum Required:

PhD in Immunology or related field
20+ years' relevant experience
15+ year leadership experience

Other Required:

Prior supervisory experience
Direct working experience and knowledge in cell based assays / bioanalysis of large or small molecule used for supporting clinical studies
A solid understanding of current GLP, GCP or GCLP standards
Working knowledge of CAP/CLIA, CLSI and ISO 13485
Experience hosting and participating in regulatory audits
Excellent communication, interpersonal, organizational and multi-tasking skills
Must be proficient with Microsoft Word, Excel, and PowerPoint
Ability to interact and function in a highly productive work environment
Ability to work independently and have good attention to detail
Must be able to read, write, speak fluently and comprehend the English language

Preferred:

Direct experience working at a CRO, Biotechnology or Pharmaceutical company.
Expertise across multiple technology platforms, including ECL, ligand-binding assays (LBA). Cell-based plate assays, flow cytometry and enzymatic activity assays,

Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice.

Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.

If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at [email protected].

Recruitment Fraud Warning: Please be aware that fraudulent individuals and websites may impersonate Precision Medicine Group or its affiliates and attempt to obtain personal, financial, or banking information through fake job postings or employment offers. Precision Medicine Group will never request payment, banking details, or other sensitive financial information as part of the recruitment process. If you believe you have been targeted by a recruitment scam, we encourage you to report the incident to your local law enforcement authorities, consumer protection agency, or relevant cybercrime reporting organization in your country. Please also notify us at [email protected] so we can investigate and take appropriate action.

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