Senior Director of Genomics Lab Operations
- Employer
- Discovery Life Sciences
- Location
- Huntsville, Alabama
- Salary
- $150,000 - $180,000
- Start date
- Sep 28, 2024
View more categoriesView less categories
- Discipline
- Clinical, Clinical Trials, Science/R&D, Biotechnology, Biotherapeutics, Cell Biology, Genomics, Infectious Disease, Laboratory, Molecular Biology, Oncology
- Required Education
- Bachelors Degree
- Position Type
- Full time
Job Details
*Relocation to Huntsville, AL required*
Position Summary:
Discovery is looking for a talented and passionate Senior Director of Genomics Lab Operations to join our dynamic Genomics team. The Senior Director will play a key role within Discovery Life Sciences Clinical and Research Services by managing the operation of the genomics testing department, ensuring the highest quality data is generated, turnaround times are met, and budgetary guidelines are maintained. We offer an exciting and collaborative work environment where you can unleash your creativity and make a real impact.
A Day in the Life of a Senior Director of Genomics Lab Operations at Discovery Life Sciences:
• Responsible for supporting oversight of the laboratory departments operational activities
• Ensures the laboratory management team adheres to written internal and external quality control.
• Guides the evaluation of means and standard deviations for quality control materials.
• Responsible for supporting oversight of the quality and timelines of technical procedures to ensure compliance with CAP/CLIA regulations, GCP/GCLP compliance.
Position Qualifications (Education, Skills, Experience):
• Bachelor's in Genomics, Molecular Biology, Immunology, or related discipline.
• Minimum of 7 years of experience in a production genomics laboratory with a high level of leadership responsibility.
• Proficient in all relevant regulatory requirements for the biopharmaceutical industry (e.g., GCP/GCLP, 21 CFR Part 11, CAP/CLIA, HIPAA)
• Strong understanding of the use of biomarkers in clinical trials driving drug development.
• Ability to lead a team to work in conformance with standard operating procedure.
• Strong project management and organizational skills, with experience prioritizing and managing projects in a biopharma setting.
• Familiarity with laboratory methods and equipment with a demonstrated ability to ensure that data generated is within specifications and to troubleshoot any abnormalities.
• Ability to communicate effectively, both verbally and written with both biopharma clients and internal stakeholders.
• Familiarity with bioinformatics tools and pipelines specific to relevant clinical data and biopharma applications is preferred.
Key Responsibilities:
• Responsible for supporting Oversight of the laboratory department's operational activities within quality and budgetary guidelines, including oversight of continuous improvements and operational updates
• Responsible for high-level management of all Proficiency Testing programs within the guidelines of regulatory requirements and pertinent SOP's.
• Provides oversight for and guides the development, implementation, and management of performance standards for staff related to quality and efficiency, including productivity.
• Ensures the laboratory management team adheres to written internal and external quality control procedures in order to maintain the quality of results. Guides the evaluation of means and standard deviations for quality control materials and ensures the maintenance of corrective action logs as appropriate.
• Responsible for supporting oversight of the quality and timelines of technical procedures to ensure full compliance with CAP/CLIA regulations, GCP/GCLP compliance, and other relevant standards as determined by the company.
• Builds strong and effective teams, valuing different contributions; works with and through others, involving people in issues that affect them. Oversee the recruitment and selection of staff
• Liaise with clients, vendors and ILS or other Discovery staff on all department issues.
• Maintains oversight of reagent and supply orders and approval of inventory purchases. Working with the corporate procurement team, negotiates pricing and service requirements with Vendor representatives, supporting the best interests of Discovery. Ensures that the laboratory management team monitors reagents and supplies for section and assists in the performance of all related tasks for managing inventory.
• Identifies the key elements of a situation and any gaps and inconsistencies in data. Makes rational judgements from available information and analysis. Actively participates in root cause analysis investigations and process improvement initiatives.
• Responsible for timely and accurate responses to Quality Issues assigned to them and/or their department.
• Identifies development opportunities for self and others; Acts as a coach and mentor and shares expertise. Maintains a positive working environment ensuring staff motivation and engagement. Maintains low levels of staff turnover, actively contributing to the retention of key individuals
• Preparing reports by collecting, analyzing, and summarizing data to identify areas of improvement on identified issues
• Supports internal and external inspections by auditors
• Establish and track departmental goals and objectives that provide world-class quality and technical services performance to the organization.
• Follow company policies and procedures, including safety and/or universal precautions.
• Respect the privacy of the personal information of patients, co-workers, and all individuals with whom the Company interacts
• Ensure compliance with all laws and regulations applicable to the Company and its operations.
• Other duties as assigned by supervisor. These may, on occasion, be unrelated to the position described here.
• Consistent and predictable attendance is an essential function of the position. Role is required on site at our Huntsville, AL, facility full-time.
Compensation and Benefits:
Discovery Life Sciences is committed to fair and equitable compensation practices, and we strive to provide employees with total compensation packages that are market competitive. The exact base pay offered for this role will depend on various factors, including but not limited to the candidate's qualifications, skills, and experience.
Your annual salary is only one part of your total compensation package. Other benefits:
• Competitive salary and benefits package options including free medical, dental, vision, life, and disability which start on your first day of employment. Free medical, dental and vision options for you and your Family members!
• 401(k) match program which starts on your first day of employment
• Flexible work hours
• Time away from work (Generous vacation and paid time off, your BIRTHDAY, paid parental leave, paid family leave, etc.).
• Professional development opportunities and reimbursement for relevant certifications.
• Collaborative and inclusive work environment that values diversity.
• Team-building activities and social events.
• Employee Referral Program and Colleague Recognition Program
Location and work hours:
• Onsite, Huntsville, AL required - relocation assistance will be provided
• Flexible work schedule
• Up to 10% travel domestic or up to 5% international travel required for mandatory site meetings and trainings
We are actively seeking motivated, dedicated individuals like you to join our thriving organization. As a leader in our industry, we offer unparalleled opportunities for professional growth and success.
Company
Discovery Life Sciences is an innovative clinical research products and services company serving the life sciences industry by delivering clinical research specimens, patient samples and human bio-fluids combined with complex annotated data sets and a wide range of clinical research services from proprietary platforms in support of novel biomarker assays, detection technologies and instrument platforms in analytical and clinical development. Our Magellan, e-commerce based, bio-repository of >200,000 specimens can ship globally within 24-48 hours.
Areas of focus include but are not limited to; infectious diseases, oncology, fetal-maternal health, cardiac diseases, autoimmune and endocrine diseases, metabolic syndrome, flu and related respiratory illness, bacterial, viral and parasitic diseases, normal control patient populations. Our Discovery Partners™ Program consists of >100 contracted clinical sites in hospital networks, academic medical centers, blood banks, clinical laboratories and community based medical practices worldwide.
Our fully integrated clinical research services include study assessment, complex protocol development, IRB submissions and approval, clinical site and principle investigator identification and selection, clinical site contracting, site monitoring, management & close out, document management, study specific collection kits, comprehensive human bio-sample program management, inventory management, cold storage, global distribution logistics.
We provide biostorage services at no charge for clients that we do clinical studies for.
Get job alerts
Create a job alert and receive personalized job recommendations straight to your inbox.
Create alert