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 ...
Sr. Medical Director, Rheumatology - US Remote
Durham, NC · Remote
$240K - $340K/yr
Industry experience inclusive of clinical trials medical monitoring experience or other relevant clinical development/trial experience at a CRO, pharmaceutical company, regulatory agency * Strong ...
Sr. Medical Director, Rheumatology - US Remote
Durham, NC · Remote
$240K - $340K/yr
Industry experience inclusive of clinical trials medical monitoring experience or other relevant clinical development/trial experience at a CRO, pharmaceutical company, regulatory agency * Strong ...
Minimum of 5 years of clinical trial experience within a CRO, pharmaceutical company, or as an industry principal investigator. An equivalent combination of appropriate education, training, and ...
Minimum of 5 years of clinical trial experience within a CRO, pharmaceutical company, or as an industry principal investigator. An equivalent combination of appropriate education, training, and ...
Inside Sales Account Manager - US - Remote
Durham, NC · On-site +1
CRO/pharmaceutical industry experience preferred, including knowledge of Phase I-IV clinical research and development * Experience with Salesforce or other CRM and sales automation tools We love ...
Inside Sales Account Manager - US - Remote
Durham, NC · On-site +1
CRO/pharmaceutical industry experience preferred, including knowledge of Phase I-IV clinical research and development * Experience with Salesforce or other CRM and sales automation tools We love ...
... CRO), pharmaceutical, or biotechnology company preferred. CRO and relevant therapeutic experience preferred Strong knowledge of Good Clinical Practice/ICH guidelines and other applicable regulatory ...
... CRO), pharmaceutical, or biotechnology company preferred. CRO and relevant therapeutic experience preferred Strong knowledge of Good Clinical Practice/ICH guidelines and other applicable regulatory ...
Inside Sales Account Manager - US - Remote
Durham, NC · On-site +1
CRO/pharmaceutical industry experience preferred, including knowledge of Phase I-IV clinical research and development * Experience with Salesforce or other CRM and sales automation tools We love ...
Inside Sales Account Manager - US - Remote
Durham, NC · On-site +1
CRO/pharmaceutical industry experience preferred, including knowledge of Phase I-IV clinical research and development * Experience with Salesforce or other CRM and sales automation tools We love ...
... CRO), pharmaceutical, or biotechnology company preferred. CRO and relevant therapeutic experience preferred Strong knowledge of Good Clinical Practice/ICH guidelines and other applicable regulatory ...
... CRO), pharmaceutical, or biotechnology company preferred. CRO and relevant therapeutic experience preferred Strong knowledge of Good Clinical Practice/ICH guidelines and other applicable regulatory ...
... CRO, pharmaceutical or biotechnology environment * Strong knowledge of clinical trial conduct, ICH-GCP guidelines and applicable regulatory requirements * Proven success leading cross-functional ...
... CRO, pharmaceutical or biotechnology environment * Strong knowledge of clinical trial conduct, ICH-GCP guidelines and applicable regulatory requirements * Proven success leading cross-functional ...
... CRO), pharmaceutical, or biotechnology company preferred. CRO and relevant therapeutic experience preferred Strong knowledge of Good Clinical Practice/ICH guidelines and other applicable regulatory ...
... CRO), pharmaceutical, or biotechnology company preferred. CRO and relevant therapeutic experience preferred Strong knowledge of Good Clinical Practice/ICH guidelines and other applicable regulatory ...
... CRO), pharmaceutical, or biotechnology company preferred. CRO and relevant therapeutic experience preferred • Strong knowledge of Good Clinical Practice/ICH guidelines and other applicable ...
... CRO), pharmaceutical, or biotechnology company preferred. CRO and relevant therapeutic experience preferred • Strong knowledge of Good Clinical Practice/ICH guidelines and other applicable ...
... CRO, pharmaceutical or biotechnology environment * Strong knowledge of clinical trial conduct, ICH-GCP guidelines and applicable regulatory requirements * Proven success leading cross-functional ...
... CRO, pharmaceutical or biotechnology environment * Strong knowledge of clinical trial conduct, ICH-GCP guidelines and applicable regulatory requirements * Proven success leading cross-functional ...
... CRO, pharmaceutical or biotechnology environment * Strong knowledge of clinical trial conduct, ICH-GCP guidelines and applicable regulatory requirements * Proven success leading cross-functional ...
... CRO, pharmaceutical or biotechnology environment * Strong knowledge of clinical trial conduct, ICH-GCP guidelines and applicable regulatory requirements * Proven success leading cross-functional ...
Sr Dir, Business Development
Durham, NC · On-site
$125.30 - $349/hr
Bachelor's Degree * 10+ years relevant industry experience (CRO/Pharmaceutical/SMO), and/or sales experience, including 10 years of management responsibility * Equivalent combination of education ...
Sr Dir, Business Development
Durham, NC · On-site
$125.30 - $349/hr
Bachelor's Degree * 10+ years relevant industry experience (CRO/Pharmaceutical/SMO), and/or sales experience, including 10 years of management responsibility * Equivalent combination of education ...
Minimum of 5 years of clinical trial experience within a CRO, pharmaceutical company, or as an industry principal investigator. An equivalent combination of appropriate education, training, and ...
New
Minimum of 5 years of clinical trial experience within a CRO, pharmaceutical company, or as an industry principal investigator. An equivalent combination of appropriate education, training, and ...
New
Business Development Director
Durham, NC · On-site
$111.20 - $309.80/hr
Qualifications * Bachelor's Degree in Business Management required * 12 years related experience, including 5 years of relevant industry (CRO/Pharmaceutical) and/or sales experience Req Or
Business Development Director
Durham, NC · On-site
$111.20 - $309.80/hr
Qualifications * Bachelor's Degree in Business Management required * 12 years related experience, including 5 years of relevant industry (CRO/Pharmaceutical) and/or sales experience Req Or
Senior Clinical Project Manager (CAR-T)
Durham, NC · On-site
$93 - $233/hr
... CRO, pharmaceutical or biotechnology environment * Strong knowledge of clinical trial conduct, ICH-GCP guidelines and applicable regulatory requirements * Proven success leading cross-functional ...
New
Senior Clinical Project Manager (CAR-T)
Durham, NC · On-site
$93 - $233/hr
... CRO, pharmaceutical or biotechnology environment * Strong knowledge of clinical trial conduct, ICH-GCP guidelines and applicable regulatory requirements * Proven success leading cross-functional ...
New
Sr Dir, Business Development
Durham, NC · On-site
$125K - $349K/yr
Bachelor's Degree * 10+ years relevant industry experience (CRO/Pharmaceutical/SMO), and/or sales experience, including 10 years of management responsibility Req Or * Equivalent combination of ...
Sr Dir, Business Development
Durham, NC · On-site
$125K - $349K/yr
Bachelor's Degree * 10+ years relevant industry experience (CRO/Pharmaceutical/SMO), and/or sales experience, including 10 years of management responsibility Req Or * Equivalent combination of ...
Prior experience in a consulting organization, CRO, pharmaceutical, or biotechnology company. Competencies * Nonclinical development strategy * Regulatory submissions and agency interactions
Prior experience in a consulting organization, CRO, pharmaceutical, or biotechnology company. Competencies * Nonclinical development strategy * Regulatory submissions and agency interactions
Prior experience in a consulting organization, CRO, pharmaceutical, or biotechnology company. Competencies * Nonclinical development strategy * Regulatory submissions and agency interactions
Prior experience in a consulting organization, CRO, pharmaceutical, or biotechnology company. Competencies * Nonclinical development strategy * Regulatory submissions and agency interactions
Cro Pharmaceutical information
See Raleigh, NC salary details
$14.02 - $15.04
4% of jobs
$15.04 - $16.06
7% of jobs
$16.06 - $17.08
10% of jobs
$17.28 is the 25th percentile. Wages below this are outliers.
$17.08 - $18.10
19% of jobs
The median wage is $18.58 / hr.
$18.10 - $19.12
20% of jobs
$19.12 - $20.14
12% of jobs
$20.65 is the 75th percentile. Wages above this are outliers.
$20.14 - $21.16
5% of jobs
$21.16 - $22.18
6% of jobs
$22.18 - $23.20
5% of jobs
$23.20 - $24.22
9% of jobs
$24.22 - $25.24
2% of jobs
$14
$19
$25
How much do cro pharmaceutical jobs pay per hour?
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.
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Cities near Raleigh, NC with the most Cro Pharmaceutical job openings:
Senior Proposal Associate - Writing - US - Remote
Durham, NC • On-site, Remote
Full-time
Re-posted 6 days ago
Job description
Who we are
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