$210K - $235K/yr
... CRO), biotechnology, or pharmaceutical environment, working to Good Laboratory Practice (GLP ... Proficient project management, presentation, and communication skills. Proficient with computers ...
$210K - $235K/yr
... CRO), biotechnology, or pharmaceutical environment, working to Good Laboratory Practice (GLP ... Proficient project management, presentation, and communication skills. Proficient with computers ...
... managing people and or leadership experience leading teams, project, programs or directing the allocation of resources * Clinical/medical research experience * 6 years of experience in a biotech ...
... managing people and or leadership experience leading teams, project, programs or directing the allocation of resources * Clinical/medical research experience * 6 years of experience in a biotech ...
Reno, NV · On-site
$17.75 - $23.25/hr
... global biotechnology and robotics company with advanced in-house manufacturing, research and ... Document Management. * Other duties as assigned. Financial Planning & Analysi s * Review and ...
Reno, NV · On-site
$17.75 - $23.25/hr
... global biotechnology and robotics company with advanced in-house manufacturing, research and ... Document Management. * Other duties as assigned. Financial Planning & Analysi s * Review and ...
Our team balances business strategy, technology, creativity, and ongoing managed services to solve ... You will design, implement and optimize medical information solutions, define project roadmaps and ...
Our team balances business strategy, technology, creativity, and ongoing managed services to solve ... You will design, implement and optimize medical information solutions, define project roadmaps and ...
$115K - $120K/yr
Demonstrated time management skills; planning and prioritization skills; ability to multi-task and ... projects and deadlines * Demonstrated effective presentation skills; ability to motivate others ...
$115K - $120K/yr
Demonstrated time management skills; planning and prioritization skills; ability to multi-task and ... projects and deadlines * Demonstrated effective presentation skills; ability to motivate others ...
Reno, NV · On-site
$115K - $120K/yr
Demonstrated time management skills; planning and prioritization skills; ability to multi-task and ... projects and deadlines * Demonstrated effective presentation skills; ability to motivate others ...
Reno, NV · On-site
$115K - $120K/yr
Demonstrated time management skills; planning and prioritization skills; ability to multi-task and ... projects and deadlines * Demonstrated effective presentation skills; ability to motivate others ...
$22.28 - $27.33
4% of jobs
$27.33 - $32.38
8% of jobs
$32.38 - $37.43
3% of jobs
$39.64 is the 25th percentile. Wages below this are outliers.
$37.43 - $42.48
21% of jobs
The median wage is $45.64 / hr.
$42.48 - $47.53
21% of jobs
$50.95 is the 75th percentile. Wages above this are outliers.
$47.53 - $52.58
25% of jobs
$52.58 - $57.64
13% of jobs
$57.64 - $62.69
2% of jobs
$62.69 - $67.74
1% of jobs
$67.74 - $72.79
1% of jobs
$72.79 - $77.84
0% of jobs
$22
$47
$77
| Aspect | Project Manager Biotech | Clinical Project Manager |
|---|---|---|
| Credentials | Bachelor's or Master's in Life Sciences, Project Management Certification | Bachelor's or Master's in Life Sciences, Clinical Research Certification |
| Work Environment | Biotech companies, R&D labs, manufacturing | Clinical trial sites, hospitals, pharmaceutical companies |
| Industry Usage | Biotech product development, research projects | Clinical trial management, regulatory compliance |
| Common Search/Comparison | Yes | Yes |
The main difference between a Project Manager Biotech and a Clinical Project Manager lies in their focus areas. The Project Manager Biotech oversees research and development projects within biotech companies, focusing on product development and manufacturing. In contrast, the Clinical Project Manager specializes in managing clinical trials, ensuring regulatory compliance and patient safety. Both roles require strong project management skills and relevant certifications, but they operate in different phases of the biotech and pharmaceutical industry.
For Project Manager Biotech jobs in Nevada, the most frequently searched job titles are:
The top searched job categories for Project Manager Biotech jobs in Nevada are:
Cities in Nevada with the most Project Manager Biotech job openings:
$210K - $235K/yr
Full-time
Medical, Retirement, PTO
Posted 24 days ago
8.4
Based on 94 frontline employees who took The Breakroom Quiz
22nd of 86 rated pharmaceutical
For 75 years, Charles River employees have worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on the health and well-being of people across the globe. Whether your background is in life sciences, finance, IT, sales or another area, your skills will play an important role in the work we perform. In return, we’ll help you build a career that you can feel passionate about.
We are seeking a Senior Director, Laboratory Sciences for our Safety Assessment site located in Reno, NV.
Direct the science and business involved in the conduct, direction and execution of Laboratory Sciences operations and studies. Provide scientific direction, oversight, and guidance to staff. Maintain and implement efficient processes and procedures to provide high quality standards of study design and timely reporting. Continue to build preclinical and clinical bioanalysis and biomarkers capabilities in an effort to expand the client base. Serve as primary expert for Laboratory Sciences within the scientific community presenting and speaking at meetings and interacting with new and perspective clients. Keep abreast and maintain a broad knowledge of state-of-the art principles and theories.
The following are responsibilities related to the Senior Director, Laboratory Sciences position:
Essential Duties and Responsibilities:Education: Masters Degree in immunology, biochemistry or a related scientific discipline required. PhD preferred.
Experience: 10 years relevant laboratory experience in a contract research organization (CRO), biotechnology, or pharmaceutical environment, working to Good Laboratory Practice (GLP) standards. 5 years management experience, including staff management and development, and financial responsibility including budgets.
Other: Management and problem solving skills. Demonstrated abilities in analytical, quantitative and critical thinking. Ability to handle multiple projects, meet deadlines and make executive level decisions. Detail oriented, flexible with the ability to work well in a team-oriented environment. Proven ability to work in a dynamic, deadline driven environment. Proficient project management, presentation, and communication skills. Proficient with computers and standard application software.
The hiring range for this position in the US is $210,000/yr - $235,000/yr. Please note that salaries vary within the range based on factors including, but not limited to, experience, skills, education, certifications, location and any collective agreements, if applicable.
About Safety Assessment
Charles River is committed to helping our partners expedite their preclinical drug development with exceptional safety assessment services, state-of-the-art facilities and expert regulatory guidance. From individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. Each year approximately 300 investigational new drug (IND) programs are conducted in our Safety Assessment facilities.
About Charles River
Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients’ clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market.
With over 20,000 employees within 110 facilities in over 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client’s unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world.
At Charles River, we are passionate about our role in improving the quality of people’s lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly worked on 80% of the drugs approved by the U.S. Food and Drug Administration (FDA) in the past five years.
We’re committed to providing benefits that elevate your quality of life. Based on your position these may include: bonus/incentives based on performance, 401K, paid time off, stock purchase program, Health and wellness coverage, employee and family wellbeing support programs, and work life balance flexibility.
Equal Employment Opportunity
Charles River is an equal opportunity employer and is committed to providing equal employment opportunities for all qualified applicants and employees without regard to race, color, sex, religion, national origin, ancestry, age, mental or physical disability, family status, pregnancy, military or veteran status, or any other characteristic protected by federal, state, or local laws.
It is unlawful in some states (including Massachusetts) to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. This contact is for accommodation requests for individuals with disabilities only and cannot be used to inquire about the status of applications.
For more information, please visit www.criver.com.
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Charles River is an early-stage contract research organization (CRO). We have built upon our foundation of laboratory animal medicine and science to develop a diverse portfolio of discovery and safety assessment services, both Good Laboratory Practice (GLP) and non-GLP, to support clients from target identification through preclinical development. Charles River also provides a suite of products and services to support our clients' clinical laboratory testing needs and manufacturing activities. Utilizing this broad portfolio of products and services enables our clients to create a more flexible drug development model, which reduces their costs, enhances their productivity and effectiveness to increase speed to market. With over 20,000 employees within 110 facilities in 20 countries around the globe, we are strategically positioned to coordinate worldwide resources and apply multidisciplinary perspectives in resolving our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic institutions around the world. At Charles River, we are passionate about our role in improving the quality of people's lives. Our mission, our excellent science and our strong sense of purpose guide us in all that we do, and we approach each day with the knowledge that our work helps to improve the health and well-being of many across the globe. We have proudly supported the development of 86% of the drugs approved by the FDA in 2021.
Scientific research and development services
10,000+ Employees
Wilmington, MA, US
1947
