Associate professor of biology job description
Updated March 14, 2024
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Example associate professor of biology requirements on a job description
Associate professor of biology requirements can be divided into technical requirements and required soft skills. The lists below show the most common requirements included in associate professor of biology job postings.
Sample associate professor of biology requirements
- Ph.D in Biology or related field.
- Minimum of two years teaching experience.
- Strong research background.
- Ability to teach at least two courses.
- Understanding of current trends in Biology.
Sample required associate professor of biology soft skills
- Excellent communication and interpersonal skills.
- Strong organizational and time management skills.
- Ability to work independently and in a team.
- Ability to make sound judgments and decisions.
Associate professor of biology job description example 1
Regeneron associate professor of biology job description
The PharmD Biologics Program (PBP) is an intensive, interdisciplinary program for graduating PharmD candidates. The program consists of training by Regeneron mentors and experience in leading projects in a variety of Global Development roles.
This unique program provides participants with depth and breadth of experience within Regeneron's Global Development organization. Throughout the program, participants will acquire technical and non-technical skills through diverse training, cross functional experiences, and ongoing mentorship. Assignments in this 2-year development program will expose candidates to critical issues and decision-making processes and acquire high level knowledge of the business and department operations, as well as gain hands-on work experience in different areas.
The program is comprised of 24-month rotational experiences within one of the following tracks:
Development Operations & Program Management (Clinical Operations) Clinical Sciences Regulatory Strategy Regulatory Labeling & Advertising/Promotion Safety Sciences
Associates will also have opportunities to gain exposure to a different functional area through an optional elective rotation as a part of the 24-month program.
In this program, you may experience:
Drafting documents integral to clinical sites and regulatory submissions Analyzing data from clinical studies in preparation for interactions with ethics committees, senior management, regulatory authorities and others Managing third-party vendors and maintaining timelines of key results Developing regulatory strategies for clinical development programs Analyzing safety data to characterize the safety profile of products throughout their development lifecycle Working with program mentors to improve skills to better reach professional goals Opportunities to travel to clinical sites and/or meetings with health authorities
This role might be for you if:
You are highly motivated and seek to build a career with a foundation in Clinical Sciences, Global Clinical Operations, Regulatory Affairs, and/or Safety Sciences You are science-minded, ask questions, and advocate for your ideas You work with precision, intellect, and integrity You are ready to work with a team that can bring great ideas to life and make a difference in the healthcare industry
To be considered for this role you must have completed your PharmD degree by Summer 2023. Industry or research experience is preferred. You are comfortable with up to 15% travel and are eligible to work in the U.S. on a permanent basis.
Application Details:
When applying please include a CV and cover letter indicating which track you are interested in applying to (may apply to more than one).
Applications accepted: October 1, 2022 - October 21, 2022
Please see the brochure for additional details on the tracks, program, and interview process.
Does this sound like you? Apply now to take your first steps toward living the Regeneron Way! We have an inclusive and diverse culture that provides amazing benefits including health and wellness programs, fitness centers and stock for eligible employees at all levels!
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, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. We will ensure that individuals with disabilities are provided reasonable accommodations to participate in the job application process. Please contact us to discuss any accommodations you think you may need.
This unique program provides participants with depth and breadth of experience within Regeneron's Global Development organization. Throughout the program, participants will acquire technical and non-technical skills through diverse training, cross functional experiences, and ongoing mentorship. Assignments in this 2-year development program will expose candidates to critical issues and decision-making processes and acquire high level knowledge of the business and department operations, as well as gain hands-on work experience in different areas.
The program is comprised of 24-month rotational experiences within one of the following tracks:
Development Operations & Program Management (Clinical Operations) Clinical Sciences Regulatory Strategy Regulatory Labeling & Advertising/Promotion Safety Sciences
Associates will also have opportunities to gain exposure to a different functional area through an optional elective rotation as a part of the 24-month program.
In this program, you may experience:
Drafting documents integral to clinical sites and regulatory submissions Analyzing data from clinical studies in preparation for interactions with ethics committees, senior management, regulatory authorities and others Managing third-party vendors and maintaining timelines of key results Developing regulatory strategies for clinical development programs Analyzing safety data to characterize the safety profile of products throughout their development lifecycle Working with program mentors to improve skills to better reach professional goals Opportunities to travel to clinical sites and/or meetings with health authorities
This role might be for you if:
You are highly motivated and seek to build a career with a foundation in Clinical Sciences, Global Clinical Operations, Regulatory Affairs, and/or Safety Sciences You are science-minded, ask questions, and advocate for your ideas You work with precision, intellect, and integrity You are ready to work with a team that can bring great ideas to life and make a difference in the healthcare industry
To be considered for this role you must have completed your PharmD degree by Summer 2023. Industry or research experience is preferred. You are comfortable with up to 15% travel and are eligible to work in the U.S. on a permanent basis.
Application Details:
When applying please include a CV and cover letter indicating which track you are interested in applying to (may apply to more than one).
Applications accepted: October 1, 2022 - October 21, 2022
Please see the brochure for additional details on the tracks, program, and interview process.
Does this sound like you? Apply now to take your first steps toward living the Regeneron Way! We have an inclusive and diverse culture that provides amazing benefits including health and wellness programs, fitness centers and stock for eligible employees at all levels!
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, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. We will ensure that individuals with disabilities are provided reasonable accommodations to participate in the job application process. Please contact us to discuss any accommodations you think you may need.
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Updated March 14, 2024