Research and Development Associate IV Job at Chickasaw Nation Industries, Inc (CNI)

Research Associate 1, In Vivo for Skeletal and CNP Therapeutic Area

We are seeking a motivated Research Associate I with in vivo experience to join ...

Location

United States , Petaluma, California

Salary:

72000.00 - 99000.00 USD / Year

BioMarin Pharmaceutical

Expiration Date

Until further notice

Requirements

Bachelor’s or equivalent scientific degree in Biology or related science
Hands-on experience with dosing and data collection in animal models of disease
Proficiency with in vivo methods such as administration of test articles, perfusion and tissue collection, blood collection
Rodent surgical experience preferred
Minimum of 2 years relevant experience
Strong analytical, problem-solving, and decision-making skills
Understanding of genetically engineered models, breeding of rodents
Excellent oral and written communication skills
Must be able to utilize computer databases for data analysis, data entry, and point of care observations
Must be able to work under time constraints with minimal direction of day-to-day responsibilities, including collaboratively working with multidisciplinary teams

Job Responsibility

Conduct in vivo dosing support and execution of studies including IV, IM, SC, IP, and PO dosing for research on genetic skeletal diseases and CNP therapeutic indications
Contribute to novel therapeutic programs
Participate and collaborate in writing, review and contribution to study synopses, protocols, study reports and regulatory documents
Collaborate with various BioMarin functions to collaboratively ensure timely progression of projects
Execute hands-on responsibilities including animal handling and restraint (rodents), administration via various routes of administration, in-life animal health monitoring and measurements, clinical observations, sample collection and processing, and accurate data collection
Provide daily care and monitoring of mice or rats, including health checks and documentation
Follow all institutional, local, and federal regulations regarding animal care and use
Adhere to safety protocols and maintain a clean and organized work environment
Maintain detailed and accurate records of all procedures and animal health status including adverse study events
Meticulous electronic lab notebook documentation

What we offer

Discretionary annual bonus
Discretionary stock-based long-term incentives
Paid time off
Company-sponsored medical, dental, vision, and life insurance plans

Fulltime

Research Associate, In Vivo

Help bring science to life and join a leading pharmaceutical company to play a k...

Location

United States , Cambridge

Salary:

36.00 - 40.00 USD / Hour

Proclinical

Expiration Date

Until further notice

Requirements

Background in biology or a related field, with hands-on experience in laboratory rodent research
Proficiency in dose administration techniques for rats and mice (e.g., SC, IV, PO, IT, IM)
Skilled in blood collection methods (e.g., tail vein, submandibular, terminal collection)
Ability to identify and document abnormal behavior and clinical signs in rodents
Strong mathematical skills for calculating dilutions and dose projections
Proficiency in MS Word, Excel, PowerPoint, and GraphPad Prism
experience with electronic data capture systems is a plus
Knowledge of rat and mouse anatomy for necropsies and tissue collections
Familiarity with applicable Animal Welfare Guidelines
Certification as an Assistant Laboratory Animal Technician (ALAT) or Laboratory Animal Technician (LAT) is advantageous

Job Responsibility

Coordinate pre-study activities, including protocol development, test article procurement, and animal ordering
Perform dose calculations and prepare dosing solutions
Conduct study procedures such as dosing, monitoring clinical signs, recording body weights, collecting blood samples, performing necropsies, and tissue collections on mice and rats
Utilize Excel spreadsheets or electronic data capture systems to collect and manage study data
Perform quality control checks on study data
Draft initial study reports and collaborate with Principal Investigators to finalize them
Create graphs of key study parameters using Excel or GraphPad Prism
Communicate effectively in group meetings and research discussions, while managing conflicts professionally
Maintain a safe and clean working environment by adhering to procedures, rules, and regulations
Adapt quickly to changing priorities in a dynamic work environment

Senior Clinical Research Associate

ICON plc is a world-leading healthcare intelligence and clinical research organi...

Location

Bulgaria , Sofia

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

University degree
CRA with a minimum of 3.5 years of independent on-site monitoring experience in a bio/pharma/CRO
Proven Skills in Site Management including management of site performance and patient recruitment
Ability to work occasionally form the sponsor's office in Sofia
Good IT skills
Ability to understand and analyze data/metrics and act appropriately
Capable of managing complex issues, works in a solution-oriented manner.

Job Responsibility

Site management and monitoring activities for assigned applicable Phase I and all Phase II-IV clinical Investigator sites
Conducts remote and onsite visits including but not limited to initiation visits, monitoring visits, close-out visits
Managing Investigator site and site activities and monitoring site data, to ensure patient safety and ethical and regulatory compliance to provide quality data required for global regulatory submissions for approval of drugs.
Managing Investigator sites to ensure the Investigator and Site Staff meet all aspects of study delivery and commitments to make certain the operational study execution is on track from site selection to site close out.
The CRA is responsible for training the Investigator and site staff on these strict regulatory regulations and procedures for timely reporting and as well as ensuring ongoing compliance.
The CRA proactively identifies potential issues and develops site Corrective Actions / Preventive Actions (CAPAs) and ensures timely and sufficient resolution of issues that may impact compliance or quality of study related activities or data.
As key contributor to the Trial Master File and study documents at the country level, ensures essential documents are appropriate and filed in a timely manner in the Investigator Site File.
Contributor in the preparation, conduct and follow up of Site Audits and Regulatory Inspections to ensure a successful outcome.

What we offer

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs.
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

Clinical Research Associate

ICON plc is a world-leading healthcare intelligence and clinical research organi...

Location

United Kingdom , Reading

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Right to work in the UK
Up to 2 years pharmaceutical/CRO industry experience
Good knowledge of drug development process specifically clinical trial/research
Knowledge of international standards (GCP/ICH, FDA, EMEA)
12+ months' monitoring experience required
Ability to travel domestically (and possibly internationally) as needed to study sites and for training and meetings
A minimum of 50% overnight travel may be required

Job Responsibility

Conducts site selection for potential sites to evaluate their capabilities for conducting a clinical trial
Recommends sites to participate in clinical trial
Is the frontline liaison between ICON and sites to ensure successful collaboration, meeting ICON expectation on milestone and deliveries
Manages assigned study sites and networks, if applicable, conducting phase I-IV protocols according to the monitoring plan and our clients procedures
Performs Site Initiation Visit, ensures site personnel is fully trained on all trial related aspects
Performs continuous training for amendments and new site personnel as required
Retrains site personnel as appropriate
Conducts continuous monitoring activities (onsite and remote)
Implements site management activities to ensure compliance with protocol, GCP, global and local regulations, global and local processes to secure data integrity and patient safety
Is accountable for continuously updating all electronic systems (global and local) relevant to perform job functions

What we offer

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs
Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others

Fulltime

Tech Associate IV

Responsible for maintaining a fleet of NPD instruments within a laboratory envir...

Location

United States , Hercules

Salary:

32.60 - 44.86 USD / Hour

Bio-Rad Laboratories

Expiration Date

Until further notice

Requirements

Bachelor's degree in Engineering or relevant technical degree
5+ years of full time work experience in relevant industry
Strong experience in diagnosing and repairing mechanical, electrical, and software systems
Proficiency in CAD design and prototype fabrication
Familiarity with embedded control systems, perception technologies, and electromechanical components
Excellent communication skills for cross-functional collaboration
Experience supporting large fleets of robots or complex automated systems

Job Responsibility

Executes basic experiments & tests
Provide assistance in Engineering tasks such as working with Engineers run Design of Experiments, Characterization and Validating Protocols
Assist with PMs, equipment service, and installation
Performs complex, directed laboratory experiments associated with the design, development, execution and implementation of scientific research projects
Research equipment and component needs, sources, competitive prices, delivery times and ongoing operational costs
Diagnoses root cause of malfunction and performs maintenance on electronic or operational equipment
Calibrates equipment and systems

What we offer

Competitive medical plans for you and your family
Free HSA funds
New fertility offering with stipend
Group life and disability
Paid parental leave
401k plus profit sharing
Employee stock purchase program
New upgraded and streamlined mental health platform
Extensive learning and development opportunities
Education benefits

Fulltime

Senior Clinical Research Associate

Clinical Research Associate ( CRAII or Senior CRA) - Remote - Romania. ICON plc ...

Location

Romania , Bucharest

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Bachelor’s Degree (or equivalent)
Minimum 3.5 years of independent on-site monitoring experience/experience as a field CRA
Ability to travel with overnight stays
Experience conducting all types of MVs such as: Site Selection, Initiation, Routine Monitoring and Close Out Visits both remotely and on-site
A demonstrated working knowledge of ICH/GCP Guidelines
Excellent record-keeping skills and attention to detail
Fluent in English and Romanian, both written and oral
Ability to travel at least 60% of the time (international and domestic - fly and drive) and should possess a valid driver’s license

Job Responsibility

Monitor multiple Phase I, II, III & IV clinical trial sites, across different therapeutic areas
Assist other team members with co-monitoring activities both remote and on-site
Utilize customer service mindset with sites focusing on delivering value, building loyalty and trust
Act as the main sponsor representative, providing key project updates
Collaborate with the team, developing commitment to study timelines and objectives through regular visits with site staff in-person and remotely
Act as the first point of contact for study sites, escalating any concerns/issues to other departments
Oversee the sites' adherence to GCP/ICH practices, ensuring quality of study conduct

What we offer

Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs
Competitive retirement planning offerings
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments

Fulltime

New

Senior Associate (In Vivo Pharmacokinetics and Drug Metabolism)

We are seeking a highly motivated, detail-oriented, and collaborative Senior Ass...

Location

United States , Thousand Oaks

Salary:

79424.85 - 107457.15 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Master's degree
Bachelor's degree with a minimum of 2 years of rodent laboratory animal research experience
Associate's degree with a minimum of 4 years of rodent laboratory animal research experience
High school diploma / GED with a minimum of 6 years of rodent laboratory animal research experience

Job Responsibility

Support senior team members in the execution of preclinical in vivo PKDM-BA studies using mouse and rat models
Assist with routine handling, restraint, husbandry support, and dosing of mice and rats through multiple administration routes including intravenous (IV), oral gavage (PO), subcutaneous (SC), and intraperitoneal (IP)
Perform biological sample collection from rodents including blood, plasma, serum, urine, feces, and tissue specimens under the guidance of experienced scientists and study leads
Conduct clinical observations, monitor rodent health and welfare, and accurately document findings in accordance with study protocols and institutional guidelines
Support rodent necropsy procedures, tissue collection and processing, and basic surgical manipulations as directed by senior staff
Prepare study materials, dosing formulations, laboratory supplies, and associated documentation to facilitate efficient study execution
Maintain accurate, organized, and compliant experimental records and laboratory documentation
Assist with laboratory organization, equipment readiness, and inventory management of research consumables and animal study supplies
Adhere to institutional animal care and use guidelines, SOPs, and laboratory safety procedures
Collaborate effectively with scientists, veterinarians, and laboratory staff to support research timelines and study objectives

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible

Fulltime

Assistant or Associate Vice President for Enrollment Management and Strategy

The Assistant/Associate Vice President for Enrollment Management and Strategy (A...

Location

United States , Kirksville

Salary:

Not provided

Buffkin / Baker

Expiration Date

Until further notice

Requirements

For the assistant level – a baccalaureate degree and strong preference for five (5) years of progressively responsible professional experience in admissions. A master’s degree is preferred.
For the associate level – a baccalaureate degree and strong preference for ten (10) years of progressively responsible professional experience in admissions. A master’s degree is preferred.
High level of skill in evaluating research and data to identify potential solutions, resolve problems, and provide information.
Demonstrated success in planning, developing, and implementing comprehensive enrollment management initiatives while collaborating with constituencies across the institution.
A sophisticated understanding of the applications of technology to the functions of enrollment management (e.g., BANNER, SLATE, AI technology, etc.).
Ability to communicate effectively with a variety of individuals, and the ability to write clearly and persuasively.
Ability to influence and mobilize a group of individuals to work toward a common goal and positively represent the mission of Truman.

Job Responsibility

Work closely with the Office of the President and the President’s Executive Leadership Team to develop a strategic planning framework for enrollment and establish and continuously improve a Strategic Enrollment Management plan that aligns with the University mission, values, and priorities as a state-designated liberal arts and sciences institution.
Ensure cross-functional collaboration to ensure all stakeholders are involved and invested in identified strategies and tactics to support healthy enrollment levels from admission through completion.
Serve as a representative and advocate, both externally and internally, related to University enrollment data and analysis, local/regional/national enrollment trends, enrollment planning, and implementation of enrollment strategies and tactics.
Ensure institutional adherence to critical federal, state, and institutional compliance mandates related to student enrollment and the functional areas of oversight.
Execute management activities that include strategic planning and decision-making
personnel management, budget and resource management
and assessment and continuous improvement of the division’s functional areas.
Create and maintain collaborative and productive partnerships across Academic Affairs, Student Engagement, administrative/systems services, and shared governance bodies to integrate effective enrollment planning and management efforts.
Effectively manage, evaluate, and provide guidance and support for professional development plans and goals for assigned areas of responsibility and assigned staff in accordance with good management practices.
Work in close partnership with Marketing and Public Relations on marketing plans for the University including outreach and advertising designed to attract and recruit students from targeted segments consistent with the University’s mission and core populations.

What we offer

Compensation will be commensurate with experience and include a base salary and a competitive benefits package.

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Research and Development Associate IV

Job Description

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