The Manager reports to either Associate Director or Director, Clinical Sciences and collaborates closely with Medical Director (MD) to provide scientific expertise necessary to design and deliver on ...
The Manager reports to either Associate Director or Director, Clinical Sciences and collaborates closely with Medical Director (MD) to provide scientific expertise necessary to design and deliver on ...
The Manager reports to either Associate Director or Director, Clinical Sciences and collaborates closely with Medical Director (MD) to provide scientific expertise necessary to design and deliver on ...
The Manager reports to either Associate Director or Director, Clinical Sciences and collaborates closely with Medical Director (MD) to provide scientific expertise necessary to design and deliver on ...
The Manager reports to either Associate Director or Director, Clinical Sciences and collaborates closely with Medical Director (MD) to provide scientific expertise necessary to design and deliver on ...
The Manager reports to either Associate Director or Director, Clinical Sciences and collaborates closely with Medical Director (MD) to provide scientific expertise necessary to design and deliver on ...
Associate Clinical Science Director
Alameda, CA · On-site
$172K - $244K/yr
In collaboration with clinical and project teams of the company, the Associate Clinical Science Director designs, plans and develops clinical evaluation research studies in oncology with focus on ...
Associate Clinical Science Director
Alameda, CA · On-site
$172K - $244K/yr
In collaboration with clinical and project teams of the company, the Associate Clinical Science Director designs, plans and develops clinical evaluation research studies in oncology with focus on ...
Associate Director, Clinical Scientist, Internal Medicine (Cardio, Metabolic, & Renal)
Tarrytown, NY · On-site
The Associate Director Clinical Sciences leads in the development, evaluation, planning and execution of clinical studies and ensures scientific integrity and interpretation of study data of a ...
Associate Director, Clinical Scientist, Internal Medicine (Cardio, Metabolic, & Renal)
Tarrytown, NY · On-site
The Associate Director Clinical Sciences leads in the development, evaluation, planning and execution of clinical studies and ensures scientific integrity and interpretation of study data of a ...
Associate Director, Clinical Scientist, Internal Medicine (Cardio, Metabolic, & Renal)
Tarrytown, NY · On-site
The Associate Director Clinical Sciences leads in the development, evaluation, planning and execution of clinical studies and ensures scientific integrity and interpretation of study data of a ...
Associate Director, Clinical Scientist, Internal Medicine (Cardio, Metabolic, & Renal)
Tarrytown, NY · On-site
The Associate Director Clinical Sciences leads in the development, evaluation, planning and execution of clinical studies and ensures scientific integrity and interpretation of study data of a ...
Associate Clinical Science Director
Alameda, CA · On-site
$172K - $244K/yr
In collaboration with clinical and project teams of the company, the Associate Clinical Science Director designs, plans and develops clinical evaluation research studies in oncology with focus on ...
Associate Clinical Science Director
Alameda, CA · On-site
$172K - $244K/yr
In collaboration with clinical and project teams of the company, the Associate Clinical Science Director designs, plans and develops clinical evaluation research studies in oncology with focus on ...
Associate Director, AI Clinical Scientist
$61K - $62K/yr
Job Summary The Associate Director, AI Clinical Scientist in the Data Science and AI team will play a pivotal role in leading strategic and technical development and use AI solutions across ...
Associate Director, AI Clinical Scientist
$61K - $62K/yr
Job Summary The Associate Director, AI Clinical Scientist in the Data Science and AI team will play a pivotal role in leading strategic and technical development and use AI solutions across ...
Associate Director, AI Clinical Scientist
Princeton, NJ · On-site
$61K - $62K/yr
Job Summary The Associate Director, AI Clinical Scientist in the Data Science and AI team will play a pivotal role in leading strategic and technical development and use AI solutions across ...
Associate Director, AI Clinical Scientist
Princeton, NJ · On-site
$61K - $62K/yr
Job Summary The Associate Director, AI Clinical Scientist in the Data Science and AI team will play a pivotal role in leading strategic and technical development and use AI solutions across ...
Additionally, the Associate Clinical Research Manager acts as liaison between senior project team ... When you join Thermo Fisher Scientific, you become part of a global team that values passion ...
Additionally, the Associate Clinical Research Manager acts as liaison between senior project team ... When you join Thermo Fisher Scientific, you become part of a global team that values passion ...
Additionally, the Associate Clinical Research Manager acts as liaison between senior project team ... When you join Thermo Fisher Scientific, you become part of a global team that values passion ...
Additionally, the Associate Clinical Research Manager acts as liaison between senior project team ... When you join Thermo Fisher Scientific, you become part of a global team that values passion ...
The Associate Director, Global Clinical Scientist provides scientific expertise necessary to design and deliver clinical studies and programs. Position Summary / Objective * Responsible for ...
The Associate Director, Global Clinical Scientist provides scientific expertise necessary to design and deliver clinical studies and programs. Position Summary / Objective * Responsible for ...
The Associate Director, Global Clinical Scientist provides scientific expertise necessary to design and deliver clinical studies and programs. Position Summary / Objective * Responsible for ...
The Associate Director, Global Clinical Scientist provides scientific expertise necessary to design and deliver clinical studies and programs. Position Summary / Objective * Responsible for ...
The Associate Director, Global Clinical Scientist provides scientific expertise necessary to design and deliver clinical studies and programs. Position Summary / Objective * Responsible for ...
The Associate Director, Global Clinical Scientist provides scientific expertise necessary to design and deliver clinical studies and programs. Position Summary / Objective * Responsible for ...
The Associate Director, Global Clinical Scientist provides scientific expertise necessary to design and deliver clinical studies and programs. Position Summary / Objective * Responsible for ...
The Associate Director, Global Clinical Scientist provides scientific expertise necessary to design and deliver clinical studies and programs. Position Summary / Objective * Responsible for ...
Additionally, the Associate Clinical Research Manager acts as liaison between senior project team ... When you join Thermo Fisher Scientific, you become part of a global team that values passion ...
Additionally, the Associate Clinical Research Manager acts as liaison between senior project team ... When you join Thermo Fisher Scientific, you become part of a global team that values passion ...
Additionally, the Associate Clinical Research Manager acts as liaison between senior project team ... When you join Thermo Fisher Scientific, you become part of a global team that values passion ...
Additionally, the Associate Clinical Research Manager acts as liaison between senior project team ... When you join Thermo Fisher Scientific, you become part of a global team that values passion ...
Clinical Development & Research - Non-MD Job Category: Scientific/Technology All Job Posting Locations: Raritan, New Jersey, United States of America The Clinical Project Scientist is responsible for ...
Clinical Development & Research - Non-MD Job Category: Scientific/Technology All Job Posting Locations: Raritan, New Jersey, United States of America The Clinical Project Scientist is responsible for ...
Associate Clinical Research Coordinator
Chapel Hill, NC · On-site
$50K - $57K/yr
... Associate Clinical Research Coordinator Position Number 20046912 Vacancy ID P021176 Full-time ... We develop and support a rich array of outstanding health sciences research programs, centers and ...
Associate Clinical Research Coordinator
Chapel Hill, NC · On-site
$50K - $57K/yr
... Associate Clinical Research Coordinator Position Number 20046912 Vacancy ID P021176 Full-time ... We develop and support a rich array of outstanding health sciences research programs, centers and ...
Assoc Dir Clinical Scientist Oncology
Raritan, NJ · On-site +1
Clinical Development & Research - Non-MD Job Category: Scientific/Technology All Job Posting Locations: Raritan, New Jersey, United States of America The Clinical Project Scientist is responsible for ...
Assoc Dir Clinical Scientist Oncology
Raritan, NJ · On-site +1
Clinical Development & Research - Non-MD Job Category: Scientific/Technology All Job Posting Locations: Raritan, New Jersey, United States of America The Clinical Project Scientist is responsible for ...
Associate Clinical Scientist information
See salary details
$28.37 - $33.22
6% of jobs
$33.22 - $38.07
13% of jobs
$40.21 is the 25th percentile. Wages below this are outliers.
$38.07 - $42.92
14% of jobs
$42.92 - $47.77
11% of jobs
The median wage is $51.27 / hr.
$47.77 - $52.62
9% of jobs
$52.62 - $57.47
18% of jobs
$57.47 - $62.33
2% of jobs
$64.14 is the 75th percentile. Wages above this are outliers.
$62.33 - $67.18
6% of jobs
$67.18 - $72.03
3% of jobs
$72.03 - $76.88
7% of jobs
$76.88 - $81.73
11% of jobs
$28
$54
$81
How much do associate clinical scientist jobs pay per hour?
What are Associate Clinical Scientists?
What are the key skills and qualifications needed to thrive as an Associate Clinical Scientist, and why are they important?
How does an Associate Clinical Scientist typically collaborate with cross-functional teams during a clinical trial?
What is the difference between Associate Clinical Scientist vs Clinical Research Associate?
| Aspect | Associate Clinical Scientist | Clinical Research Associate |
|---|---|---|
| Required Credentials | Bachelor's or Master's in life sciences, relevant certifications | Bachelor's in life sciences, often with certifications in clinical trials |
| Work Environment | Research labs, pharmaceutical companies, biotech firms | Clinical trial sites, hospitals, research organizations |
| Employer & Industry Usage | Pharmaceutical, biotech, medical device companies | Contract research organizations, pharmaceutical companies |
| Common Search & Comparison | Yes | Yes |
The Associate Clinical Scientist and Clinical Research Associate roles share similarities in industry and required credentials, but differ mainly in work environment and focus. The Associate Clinical Scientist typically works in research labs or biotech firms focusing on data analysis and scientific development, while the Clinical Research Associate is more involved in monitoring clinical trials at trial sites. Both roles are essential in the clinical research process, with overlapping skills and industry usage.

Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Re-posted 11 days ago
Regeneron rating
8.7
Based on 42 frontline employees who took The Breakroom Quiz
12th of 74 rated pharmaceutical
Job description
The Manager, Clinical Sciences, Hematology leads in the development, evaluation, planning and execution of clinical studies and ensures scientific integrity and interpretation of study data of a clinical development program. The Senior Manager leads in a matrix environment as part of a cross-functional team and may contribute to candidate development projects through early and/or late phase development. The Manager reports to either Associate Director or Director, Clinical Sciences and collaborates closely with Medical Director (MD) to provide scientific expertise necessary to design and deliver on clinical studies and programs.
As a Manager, a typical day may include the following:
Member of the Clinical Study Team and Global Clinical sub-team
Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings; may represent function in collaborative activities with other departments
Develops/maintains proficient understanding of therapeutic disease area(s) and drug candidate including underlying disease biology, clinical manifestations and therapeutic standard practice, compound(s) including mechanism of action and drug landscape
Applies basic scientific expertise to support initiation and execution of clinical research and development studies for early and/or late-stage assets
Assists with development of the Expanded Synopsis and may author clinically relevant sections and reviews other scientific portions of clinical trial protocols and amendments
Assists with and may authors/review documents related to trials, such as medical monitoring plans, SAPs, informed consents and clinical components of the Clinical Study Reports and may support development of regulatory documents; may perform quality review
Maintains compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety
Contributes to preparations for external /stakeholder meetings (IM, Governance, DMCs, Regulatory Authority). Presents data and information to external investigators (SIV) and internal collaborators
This role may be for you if:
Possess demonstrated knowledge of the drug development process, Good Clinical Practice, study design, clinical research methodology & demonstrate solid medical writing skills
Proven ability to influence within team and may influence across functionally
Exhibit strong analytical and influencing skills; ability to communicate concise and clear messages, strong presentation skills
Independently uses professional concepts and company objectives to resolve complex issues in creative and effective ways
To be considered for this position, you must have a minimum of Bachelor's Degree required; Advanced degree or equivalent education/degree in life science/healthcare preferred (PhD/MD/PharmD/MSc). We are seeking a minimum of 3 years of pharmaceutical clinical drug development experience. Other levels considered depending on experience. You have a basic knowledge of oncology or hematology therapeutic areas as well as a proven track in clinical trial process improvements. We need an individual with demonstrated leadership and accomplishment in all aspects of conducting global clinical trials and execution of clinical programs. Proficient knowledge of clinical development process, regulatory requirements and ICH/GCP guidelines. Resolves novel problems requiring creative application of advanced skill, training, and education.
Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.
Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.
Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed onsite. Please speak with your recruiter and hiring manager for more information about onsite expectations for your role and location.
As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.
For jobs in Canada: this posting is for an existing position.
Salary Range (annually)
$128,600.00 - $210,000.00What Regeneron employees say
Pay
Benefits
Hours and flexibility
Workplace
Get the full story on Breakroom
About Regeneron
Sourced by ZipRecruiter
Industry
Biotechnology research and development
Company size
5,001 - 10,000 Employees
Headquarters location
Tarrytown, NY, US
Year founded
1988