Minimum two years' experience in CRO/pharmaceutical business development or operational, academic, or corporate environment or as a Proposal Associate - Writing. * Bachelor's degree; master's or PhD ...
Minimum two years' experience in CRO/pharmaceutical business development or operational, academic, or corporate environment or as a Proposal Associate - Writing. * Bachelor's degree; master's or PhD ...
Minimum two years' experience in CRO/pharmaceutical business development or operational, academic, or corporate environment or as a Proposal Associate - Writing. * Bachelor's degree; master's or PhD ...
Minimum two years' experience in CRO/pharmaceutical business development or operational, academic, or corporate environment or as a Proposal Associate - Writing. * Bachelor's degree; master's or PhD ...
CSV Engineer
Redwood City, CA ยท On-site
Katalyst CRO is looking for an experienced and well-rounded CSV (Computer System Validation) Consultant to support multiple ongoing projects within a pharmaceutical environment. The ideal candidate ...
CSV Engineer
Redwood City, CA ยท On-site
Katalyst CRO is looking for an experienced and well-rounded CSV (Computer System Validation) Consultant to support multiple ongoing projects within a pharmaceutical environment. The ideal candidate ...
CRO Partner Manager Duration: 12Months Location: Whippany, NJ 07981 Alliance Management is part of ... BA or BS in a pharmaceutical development related field Requirements: * 5-7 years' experience in ...
CRO Partner Manager Duration: 12Months Location: Whippany, NJ 07981 Alliance Management is part of ... BA or BS in a pharmaceutical development related field Requirements: * 5-7 years' experience in ...
CRO Partner Manager Duration: 12Months Location: Whippany, NJ 07981 Alliance Management is part of ... BA or BS in a pharmaceutical development related field Requirements: * 5-7 years' experience in ...
CRO Partner Manager Duration: 12Months Location: Whippany, NJ 07981 Alliance Management is part of ... BA or BS in a pharmaceutical development related field Requirements: * 5-7 years' experience in ...
Bachelor's degree in science related field, advanced degree preferred. * 10+ years' experience within CRO, pharmaceutical, biologics, or animal health industry. * Demonstrated success leading ...
Bachelor's degree in science related field, advanced degree preferred. * 10+ years' experience within CRO, pharmaceutical, biologics, or animal health industry. * Demonstrated success leading ...
Bachelor's degree in science related field, advanced degree preferred. * 10+ years' experience within CRO, pharmaceutical, biologics, or animal health industry. * Demonstrated success leading ...
Bachelor's degree in science related field, advanced degree preferred. * 10+ years' experience within CRO, pharmaceutical, biologics, or animal health industry. * Demonstrated success leading ...
Katalyst CRO is seeking a Computer System Validation (CSV) Engineer for a global pharmaceutical client. This role involves leading and executing validation activities for GxP electronic systems and ...
Katalyst CRO is seeking a Computer System Validation (CSV) Engineer for a global pharmaceutical client. This role involves leading and executing validation activities for GxP electronic systems and ...
Regulatory Strategy, Vice President (Bay Area, Boston) (California)
California, MO ยท On-site
$200K/yr
Minimum fifteen years of regulatory experience in the pharmaceutical, CRO, biotechnology, or consulting industry, involving regulatory submissions in drug development. * At least seven years of which ...
Regulatory Strategy, Vice President (Bay Area, Boston) (California)
California, MO ยท On-site
$200K/yr
Minimum fifteen years of regulatory experience in the pharmaceutical, CRO, biotechnology, or consulting industry, involving regulatory submissions in drug development. * At least seven years of which ...
Bachelor's degree required; 2-3 years of experience in a CRO, Pharmaceutical or lab sales industry experience * Salary and Benefits : Frontage Laboratories offers a competitive compensation and ...
Quick apply
Bachelor's degree required; 2-3 years of experience in a CRO, Pharmaceutical or lab sales industry experience * Salary and Benefits : Frontage Laboratories offers a competitive compensation and ...
CRO(Contract Research Organizations) Job Summary The Global Category Management for Contract ... pharmaceutical industry. * Proven experience in developing and implementing global category ...
CRO(Contract Research Organizations) Job Summary The Global Category Management for Contract ... pharmaceutical industry. * Proven experience in developing and implementing global category ...
Only Green Card or Citizens local to New Jersey 9-11 years of experience in a pharmaceutical company/CRO with business analyst along with project management Strong understanding/knowledge on clinical ...
Only Green Card or Citizens local to New Jersey 9-11 years of experience in a pharmaceutical company/CRO with business analyst along with project management Strong understanding/knowledge on clinical ...
Katalyst CRO is seeking a Computer System Validation (CSV) Engineer for a global pharmaceutical client. This role will lead and execute validation activities for GxP electronic systems and ...
Katalyst CRO is seeking a Computer System Validation (CSV) Engineer for a global pharmaceutical client. This role will lead and execute validation activities for GxP electronic systems and ...
Associate QC Specialist
Exton, PA ยท On-site
Experience * 0-3 years of experience in a bioanalytical laboratory, biomarker research, or quality control role in a CRO, pharmaceutical, or biotechnology environment. * Experience with GLP-regulated ...
Quick apply
Associate QC Specialist
Exton, PA ยท On-site
Experience * 0-3 years of experience in a bioanalytical laboratory, biomarker research, or quality control role in a CRO, pharmaceutical, or biotechnology environment. * Experience with GLP-regulated ...
CSV Engineer
Somerset, NJ ยท On-site
... CRO) dedicated to driving innovation in research, regulatory compliance, and quality excellence for pharmaceutical, biotechnology, and medical device companies worldwide. Founded in , the company is ...
CSV Engineer
Somerset, NJ ยท On-site
... CRO) dedicated to driving innovation in research, regulatory compliance, and quality excellence for pharmaceutical, biotechnology, and medical device companies worldwide. Founded in , the company is ...
Regulatory Strategy, Vice President (Bay Area, Boston)
California, MO ยท On-site
$180 - $220/hr
Minimum fifteen years of regulatory experience in the pharmaceutical, CRO, biotechnology, or consulting industry, involving regulatory submissions in drug development. * At least seven years of which ...
Regulatory Strategy, Vice President (Bay Area, Boston)
California, MO ยท On-site
$180 - $220/hr
Minimum fifteen years of regulatory experience in the pharmaceutical, CRO, biotechnology, or consulting industry, involving regulatory submissions in drug development. * At least seven years of which ...
Business Development Director - Preclinical CRO
Princeton, NJ ยท Remote
$110K - $150K/yr
Vision insurance Medicilon is a leading integrated Contract Research Organization (CRO) providing comprehensive preclinical R&D services to pharmaceutical and biotechnology companies, as well as ...
Quick apply
Business Development Director - Preclinical CRO
Princeton, NJ ยท Remote
$110K - $150K/yr
Vision insurance Medicilon is a leading integrated Contract Research Organization (CRO) providing comprehensive preclinical R&D services to pharmaceutical and biotechnology companies, as well as ...
Director Talent Acquisition - US
$106K - $146K/yr
The successful candidate will bring deep expertise in recruiting within the CRO, pharmaceutical, biotechnology, or clinical research sectors, along with proven experience leading geographically ...
Director Talent Acquisition - US
$106K - $146K/yr
The successful candidate will bring deep expertise in recruiting within the CRO, pharmaceutical, biotechnology, or clinical research sectors, along with proven experience leading geographically ...
CSV Engineer
Somerset, NJ ยท On-site
... CRO) dedicated to driving innovation in research, regulatory compliance, and quality excellence for pharmaceutical, biotechnology, and medical device companies worldwide. Founded in , the company is ...
CSV Engineer
Somerset, NJ ยท On-site
... CRO) dedicated to driving innovation in research, regulatory compliance, and quality excellence for pharmaceutical, biotechnology, and medical device companies worldwide. Founded in , the company is ...
Vice President, Global Medical Affairs
Covington, KY ยท On-site +1
What You'll Bring: * 10 years of progressive experience in the CRO, pharmaceutical or biotech industry. * Significant clinical research experience including medical monitoring. * Deep scientific ...
Vice President, Global Medical Affairs
Covington, KY ยท On-site +1
What You'll Bring: * 10 years of progressive experience in the CRO, pharmaceutical or biotech industry. * Significant clinical research experience including medical monitoring. * Deep scientific ...
Cro Pharmaceutical information
See salary details
$14.42 - $15.47
4% of jobs
$15.47 - $16.52
7% of jobs
$16.52 - $17.57
10% of jobs
$17.77 is the 25th percentile. Wages below this are outliers.
$17.57 - $18.62
19% of jobs
The median wage is $19.12 / hr.
$18.62 - $19.67
20% of jobs
$19.67 - $20.72
12% of jobs
$21.24 is the 75th percentile. Wages above this are outliers.
$20.72 - $21.77
5% of jobs
$21.77 - $22.81
6% of jobs
$22.81 - $23.86
5% of jobs
$23.86 - $24.91
9% of jobs
$24.91 - $25.96
2% of jobs
$14
$19
$25
How much do cro pharmaceutical jobs pay per hour?
What jobs pay $500,000 a year in the US?
What is the difference between Cro Pharmaceutical vs Clinical Research Associate?
| Aspect | Cro Pharmaceutical | Clinical Research Associate |
|---|---|---|
| Credentials | Typically requires a degree in pharmacy, life sciences, or related field | Requires a degree in life sciences, healthcare, or related field; certifications like CCRA are common |
| Work Environment | Pharmaceutical companies, research labs, manufacturing facilities | Clinical trial sites, hospitals, research organizations |
| Industry Usage | Used in pharmaceutical manufacturing, quality control, and regulatory compliance | Involved in monitoring clinical trials, ensuring protocol adherence |
While Cro Pharmaceutical focuses on manufacturing, quality assurance, and regulatory aspects within the pharmaceutical industry, Clinical Research Associates primarily oversee clinical trial processes. Both roles require scientific backgrounds and industry experience but differ in daily responsibilities and work settings.
What does a CRO do in pharma?
What is the highest paying job in pharmaceuticals?
Is it better to work for a CRO or pharmaceutical company?
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Senior Proposal Associate - Writing - US - Remote
Durham, NC โข On-site, Remote
Full-time
Posted 18 days ago
Job description
We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.
Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.
Why Worldwide
We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!
What the Senior Proposal Associate - Writing does at Worldwide
The Senior Proposal Associate - Writing role leads proposal writing responsibilities for assigned projects, supports our overall content management, and completes additional proposal writing team tasks as needed. The Senior Proposal Associate - Writing role works with Account Directors, subject matter experts (SMEs), Proposal Managers, and other Worldwide personnel.
What you will do
- Develop robust proposals, leading the writing, coordination, and presentation of our responses in Microsoft Word, PowerPoint, and other systems/formats.
- Work with Account Directors and SMEs to effectively manage the proposal development process.
- Actively participate in project strategy discussions, ensuring product/service offerings are clearly articulated in proposals.
- Proofread, edit, rewrite, and revise documents to ensure readability, consistency, accuracy, and relevance.
- Meet proposal deadlines by establishing priorities and target dates for information gathering, writing, reviews, approvals, and signatures.
- Act as a focal point to collect information from various sources.
What you will bring to the role
- Effective planning, strategizing, managing, monitoring, scheduling, and critiquing skills.
- Compelling written and verbal communication skills to clearly and concisely present information.
- Strong interpersonal skills to work in a dynamic team with various personnel in a fast-paced, deadline-oriented environment. Frequent interaction with internal customers required.
- Ability to handle multiple short-term assignments and project deliverables with strict deadlines in a constantly dynamic environment.
- Ability to exercise sound judgment and make decisions independently.
Your experience
- Robust writing, project management, and time management skills to complete proposals on time and with high quality.
- Minimum two years' experience in CRO/pharmaceutical business development or operational, academic, or corporate environment or as a Proposal Associate - Writing.
- Bachelor's degree; master's or PhD preferred (prefer degree in Life Sciences, Communications, Journalism, or Marketing).
- Experience drafting RFIs in a CRO environment, or in pharma/biotech outsourcing preferred.
- Knowledge of the CRO/pharmaceutical industry, knowledge of sales support activities, and an understanding of study design, project management, and operational requirements for successful study implementation.
- Ability to advise and interact with all levels of management.
- Strong customer relationship management skills and strong commercial acumen.
At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation.
The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates):
United States of America - $65,000.00 - $129,000.00
The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage.
We love knowing that someone is going to have a better life because of the work we do.
To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.
About Worldwide Clinical Trials
Sourced by ZipRecruiter
Industry
Scientific research and development services
Company size
10,000+ Employees
Headquarters location
Durham, NC, US
Year founded
1986