1

Cro Pharmaceutical Jobs in Raleigh, NC (NOW HIRING)

... 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 ...

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 ...

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

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 ...

next page

Showing results 1-20

Cro Pharmaceutical information

See Raleigh, NC salary details

$14

$19

$25

How much do cro pharmaceutical jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for cro pharmaceutical in Raleigh, NC is $19.23, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $21.25 per hour, depending on experience, location, and employer.

What is the difference between Cro Pharmaceutical vs Clinical Research Associate?

AspectCro PharmaceuticalClinical Research Associate
CredentialsTypically requires a degree in pharmacy, life sciences, or related fieldRequires a degree in life sciences, healthcare, or related field; certifications like CCRA are common
Work EnvironmentPharmaceutical companies, research labs, manufacturing facilitiesClinical trial sites, hospitals, research organizations
Industry UsageUsed in pharmaceutical manufacturing, quality control, and regulatory complianceInvolved 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.

Is CRO a good career?

A career as a CRO (Contract Research Organization) professional involves working in clinical research, often requiring knowledge of regulatory standards, data management, and trial processes. It can offer opportunities in the pharmaceutical and biotech industries with roles in project management, monitoring, and data analysis. The field generally provides stable employment with potential for advancement and specialization.

What are popular job titles related to Cro Pharmaceutical jobs in Raleigh, NC?

For Cro Pharmaceutical jobs in Raleigh, NC, the most frequently searched job titles are:

What cities near Raleigh, NC are hiring for Cro Pharmaceutical jobs?

Cities near Raleigh, NC with the most Cro Pharmaceutical job openings:

Senior Proposal Associate - Writing - US - Remote

Worldwide Clinical Trials

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.