Manage processing and Characterization of samples obtained from in vivo studies. Execute soluble protein isolation and analysis via bead-based multiplex platform. Execute mRNA isolation and ...
Manage processing and Characterization of samples obtained from in vivo studies. Execute soluble protein isolation and analysis via bead-based multiplex platform. Execute mRNA isolation and ...
Associate Director/Director, In Vivo Physiology
South San Francisco, CA · On-site
$215K - $265K/yr
Lead preclinical physiology team that develops and executes program-specific and indication-specific in vivo studies * Mentor scientists and associate scientists to effectively serve as translational ...
Associate Director/Director, In Vivo Physiology
South San Francisco, CA · On-site
$215K - $265K/yr
Lead preclinical physiology team that develops and executes program-specific and indication-specific in vivo studies * Mentor scientists and associate scientists to effectively serve as translational ...
Study Coordinator, Preclinical Research
Carlsbad, CA · On-site
$27 - $33/hr
Strong experience in in vivo / preclinical research environments * Hands-on experience with study coordination, data management, or research operations * Familiarity with electronic systems such as ...
Study Coordinator, Preclinical Research
Carlsbad, CA · On-site
$27 - $33/hr
Strong experience in in vivo / preclinical research environments * Hands-on experience with study coordination, data management, or research operations * Familiarity with electronic systems such as ...
Lead preclinical physiology team that develops and executes program-specific and indication-specific in vivo studies * Mentor scientists and associate scientists to effectively serve as translational ...
Lead preclinical physiology team that develops and executes program-specific and indication-specific in vivo studies * Mentor scientists and associate scientists to effectively serve as translational ...
In Vivo Research Associate
Boston, MA · On-site
$30 - $34/hr
Independently plan experiments and document study data Qualifications The successful candidate will ... with Manager and/or Group Leader * 45-60 Meeting In-Person. on-site to meet with the Team The ...
In Vivo Research Associate
Boston, MA · On-site
$30 - $34/hr
Independently plan experiments and document study data Qualifications The successful candidate will ... with Manager and/or Group Leader * 45-60 Meeting In-Person. on-site to meet with the Team The ...
Research Associate/Senior Research Associate, In Vivo Pharmacology
Cambridge, MA · On-site
$96K - $110K/yr
Execute in vivo studies using selected mouse models to assess the efficacy and tumorigenicity risk of thymic cell product following engraftment. * Perform standard dosing procedures (SC, IM, IV, IP ...
Quick apply
Research Associate/Senior Research Associate, In Vivo Pharmacology
Cambridge, MA · On-site
$96K - $110K/yr
Execute in vivo studies using selected mouse models to assess the efficacy and tumorigenicity risk of thymic cell product following engraftment. * Perform standard dosing procedures (SC, IM, IV, IP ...
This role will focus on developing program-specific in vivo pharmacology strategies, establishing ... Manage relationships with CROs and external collaborators to ensure high-quality study execution ...
This role will focus on developing program-specific in vivo pharmacology strategies, establishing ... Manage relationships with CROs and external collaborators to ensure high-quality study execution ...
This role will focus on developing program-specific in vivo pharmacology strategies, establishing ... Manage relationships with CROs and external collaborators to ensure high-quality study execution ...
Quick apply
This role will focus on developing program-specific in vivo pharmacology strategies, establishing ... Manage relationships with CROs and external collaborators to ensure high-quality study execution ...
In Vivo Research Associate
Boston, MA · On-site
$30 - $34/hr
Independently plan experiments and document study data Qualifications The successful candidate will ... with Manager and/or Group Leader * 45-60 Meeting In-Person. on-site to meet with the Team The ...
In Vivo Research Associate
Boston, MA · On-site
$30 - $34/hr
Independently plan experiments and document study data Qualifications The successful candidate will ... with Manager and/or Group Leader * 45-60 Meeting In-Person. on-site to meet with the Team The ...
Conduct in vivo mouse studies, including dosing via IV, IP, SQ, and other routes as needed. * Perform necropsy, tissue dissection, perfusion, and blood/tissue collection (in-life and terminal
Conduct in vivo mouse studies, including dosing via IV, IP, SQ, and other routes as needed. * Perform necropsy, tissue dissection, perfusion, and blood/tissue collection (in-life and terminal
In Vivo Research Associate
$30 - $34/hr
Independently plan experiments and document study data Qualifications The successful candidate will ... with Manager and/or Group Leader * 45-60 Meeting In-Person. on-site to meet with the Team The ...
In Vivo Research Associate
$30 - $34/hr
Independently plan experiments and document study data Qualifications The successful candidate will ... with Manager and/or Group Leader * 45-60 Meeting In-Person. on-site to meet with the Team The ...
Associate Scientist, In Vivo Pharmacology
Redwood City, CA · On-site
$119K - $128K/yr
Contribute to study planning, experimental timelines, and data-driven decision making for program advancement  * Maintain accurate, well-organized experimental records while ensuring a safe ...
Quick apply
Associate Scientist, In Vivo Pharmacology
Redwood City, CA · On-site
$119K - $128K/yr
Contribute to study planning, experimental timelines, and data-driven decision making for program advancement  * Maintain accurate, well-organized experimental records while ensuring a safe ...
This role will focus on developing program-specific in vivo pharmacology strategies, establishing ... Manage relationships with CROs and external collaborators to ensure high-quality study execution ...
This role will focus on developing program-specific in vivo pharmacology strategies, establishing ... Manage relationships with CROs and external collaborators to ensure high-quality study execution ...
The Lab Technician IV - In Vivo Research will play a key role in supporting preclinical studies and high-containment laboratory operations for a leading government-affiliated research program.
The Lab Technician IV - In Vivo Research will play a key role in supporting preclinical studies and high-containment laboratory operations for a leading government-affiliated research program.
Associate Director, GLP Study Management
$180K - $205K/yr
We are seeking an accomplished Senior/Associate Director to lead nonclinical safety study management (Toxicology and Bioanalytical), driving the operational execution of in vitro and in vivo safety ...
New
Quick apply
Associate Director, GLP Study Management
$180K - $205K/yr
We are seeking an accomplished Senior/Associate Director to lead nonclinical safety study management (Toxicology and Bioanalytical), driving the operational execution of in vitro and in vivo safety ...
New
Study Director: Translational Oncology
San Diego, CA · On-site
$90K - $120K/yr
D. in Life Science related field preferred, MS required * 3 years experience in managing oncology-related assays, and/or in-vivo immunology, pharmacology or related scientific studies * Experience ...
Quick apply
Study Director: Translational Oncology
San Diego, CA · On-site
$90K - $120K/yr
D. in Life Science related field preferred, MS required * 3 years experience in managing oncology-related assays, and/or in-vivo immunology, pharmacology or related scientific studies * Experience ...
Associate Director, GLP Study Management
$180K - $205K/yr
We are seeking an accomplished Senior/Associate Director to lead nonclinical safety study management (Toxicology and Bioanalytical), driving the operational execution of in vitro and in vivo safety ...
New
Associate Director, GLP Study Management
$180K - $205K/yr
We are seeking an accomplished Senior/Associate Director to lead nonclinical safety study management (Toxicology and Bioanalytical), driving the operational execution of in vitro and in vivo safety ...
New
Works closely with Study Directors, Study Coordinators and cross functional team members to ensure ... Perform advanced in vivo procedures (including sample collection, surgeries.) with minimal direct ...
Works closely with Study Directors, Study Coordinators and cross functional team members to ensure ... Perform advanced in vivo procedures (including sample collection, surgeries.) with minimal direct ...
Director/Senior Director, In Vivo Pharmacology
San Francisco, CA · On-site
$195K - $290K/yr
Lead the in vivo pharmacology strategy for Rezo's small-molecule oncology programs, including study ... Strong CRO management experience, including protocol design, study oversight, data QC, ...
Quick apply
Director/Senior Director, In Vivo Pharmacology
San Francisco, CA · On-site
$195K - $290K/yr
Lead the in vivo pharmacology strategy for Rezo's small-molecule oncology programs, including study ... Strong CRO management experience, including protocol design, study oversight, data QC, ...
Director/Senior Director, In Vivo Pharmacology
San Francisco, CA · On-site
$195K - $290K/yr
Lead the in vivo pharmacology strategy for Rezo's small-molecule oncology programs, including study ... Strong CRO management experience, including protocol design, study oversight, data QC, ...
Director/Senior Director, In Vivo Pharmacology
San Francisco, CA · On-site
$195K - $290K/yr
Lead the in vivo pharmacology strategy for Rezo's small-molecule oncology programs, including study ... Strong CRO management experience, including protocol design, study oversight, data QC, ...
In Vivo Study Manager information
What are some common challenges faced by In Vivo Study Managers, and how can they be addressed?
In Vivo Study Managers often encounter challenges such as coordinating complex study timelines, ensuring regulatory compliance, and managing cross-functional teams. Balancing the demands of multiple studies while maintaining high standards for animal welfare and data integrity can also be demanding. Effective communication, strong organizational skills, and proactive problem-solving are essential for overcoming these challenges. Establishing clear protocols and fostering collaboration between research, veterinary, and regulatory teams can help streamline operations and ensure successful study outcomes.
What are the key skills and qualifications needed to thrive as an In Vivo Study Manager, and why are they important?
To thrive as an In Vivo Study Manager, you need a solid background in animal science, pharmacology, or related biological sciences, typically supported by a relevant degree and experience in preclinical research. Familiarity with laboratory animal management systems, regulatory compliance tools (such as GLP), and data analysis software is essential. Strong organizational skills, attention to detail, leadership, and effective communication are standout soft skills for coordinating study teams and reporting results. These competencies are crucial for ensuring ethical, efficient, and high-quality execution of in vivo studies in compliance with regulatory standards.
What is the difference between In Vivo Study Manager vs In Vivo Study Coordinator?
| Aspect | In Vivo Study Manager | In Vivo Study Coordinator |
|---|---|---|
| Responsibilities | Oversees entire in vivo studies, manages teams, ensures protocol compliance | Assists with daily study tasks, prepares materials, supports study execution |
| Required Credentials | Bachelor's or higher in life sciences, experience in study management | Relevant degree, experience in laboratory or clinical settings |
| Work Environment | Research labs, clinical facilities, project management settings | Laboratories, research facilities, clinical trial sites |
| Industry Usage | Commonly used in pharmaceutical, biotech, and research organizations | Often found in similar settings, supporting study teams |
The In Vivo Study Manager typically leads and oversees entire studies, requiring more experience and management skills. The In Vivo Study Coordinator supports daily operations and assists managers, focusing on execution rather than leadership. Both roles are essential in research settings, but the manager has broader responsibilities and higher qualifications.
What does an In Vivo Study Manager do?
An In Vivo Study Manager is responsible for planning, overseeing, and coordinating research studies that involve live animal models to evaluate the efficacy, safety, and pharmacology of new drugs or treatments. They ensure that all experiments comply with regulatory guidelines and ethical standards, manage study timelines and budgets, and supervise laboratory staff. Additionally, they analyze study data, prepare reports, and communicate findings to project teams or regulatory bodies.
Job description
Company Description
A Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.
This is Contract position with my direct clientÂ
Job Description
Job Responsibilities:
The candidate will work in a research environment in support of discoveries in immunology and inflammation.Â
The individual will be actively involved in laboratory work related to the dosing and sampling of molecules, raw materials, and-or blood and tissues for the determination of pharmacokinetic properties of new therapeutics coming from various research targets through in vivo experimentation.Â
As such, the individual will need to have a broad understanding of drug administration and sampling techniques.Â
The individual will also need experience in IACUC standards and requirements.Â
Experience with rodents is required.
Qualifications
Interact with vivarium staff to coordinate in vivo study execution and sample acquisition.
Manage processing and Characterization of samples obtained from in vivo studies.
Execute soluble protein isolation and analysis via bead-based multiplex platform.
Execute mRNA isolation and expression characterization via quantitative real time PCR.
Mammalian cell culture and aseptic technique.
Ability to manage workload, coordinate in vivo studies and prioritize tasks.
Demonstration of oral, written and interpersonal skills including the ability to document and effectively communicate interpretation of data and results.Â
BS with 5 years' experience or MS with 2 year experience
Additional Information
Contact me at 732 429 1924 ORÂ 732 549 2030*244Â
About Integrated Resources
Sourced by ZipRecruiter
Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.
Industry
Recruiting and staffing services
Company size
51 - 200 Employees
Headquarters location
Edison, NJ, US
Year founded
1996