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Every Cure Jobs in Raleigh, NC (NOW HIRING)

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Every Cure information

See Raleigh, NC salary details

$33.5K

$55.8K

$89.4K

How much do every cure jobs pay per year?

As of Aug 22, 2026, the average yearly pay for every cure in Raleigh, NC is $55,763.00, according to ZipRecruiter salary data. Most workers in this role earn between $41,800.00 and $67,600.00 per year, depending on experience, location, and employer.

What is Every Cure?

Every Cure is a nonprofit organization focused on systematically identifying and advancing new uses for existing medicines to treat diseases. They use advanced data analytics, artificial intelligence, and partnerships with researchers to uncover potential new treatment options for patients. By leveraging existing drugs, Every Cure aims to accelerate the availability of therapies and reduce the time and cost associated with developing new medicines. Their ultimate goal is to maximize the impact of existing treatments on global health.

What are the key skills and qualifications needed to thrive as a clinical research scientist, and why are they important?

To thrive as a Clinical Research Scientist, you need a solid background in life sciences, clinical trial design, and data analysis, typically supported by an advanced degree such as a PhD or PharmD. Familiarity with regulatory guidelines, statistical software (like SAS or SPSS), and electronic data capture systems is crucial. Strong analytical thinking, attention to detail, and effective communication skills help you manage studies and present findings clearly. These capabilities ensure rigorous, compliant research and the successful advancement of new therapies.

What are some typical challenges faced by professionals working in drug repurposing research at Every Cure?

Professionals at Every Cure often encounter the challenge of navigating complex regulatory pathways while identifying and validating new applications for existing drugs. The role requires close collaboration with interdisciplinary teams, including data scientists, clinicians, and regulatory experts, to efficiently analyze large datasets and design clinical studies. Additionally, securing funding and managing stakeholder expectations can be demanding, as drug repurposing projects must demonstrate clear scientific and business potential. Despite these challenges, the work environment is highly collaborative and mission-driven, offering opportunities to make a significant impact on patient outcomes.

What is the difference between Every Cure vs Pharmacist?

AspectEvery CurePharmacist
Required CredentialsCertification in alternative medicine or holistic healthDoctor of Pharmacy (PharmD) degree, state licensure
Work EnvironmentClinics, wellness centers, online platformsHospitals, retail pharmacies, clinics
Industry UsageComplementary and alternative medicine industryHealthcare and pharmaceutical industry
Common Search IntentAlternative health solutions, holistic treatmentsMedication dispensing, health consultations

Every Cure typically focuses on holistic and alternative health methods, often requiring certifications in natural or complementary medicine. Pharmacists, on the other hand, are licensed healthcare professionals with a PharmD degree, working mainly in pharmacies and healthcare settings. While both roles are involved in health and wellness, their credentials, work environments, and industry usage differ significantly.

What are popular job titles related to Every Cure jobs in Raleigh, NC?

For Every Cure jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Every Cure jobs in Raleigh, NC look for?

The top searched job categories for Every Cure jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Every Cure jobs?

Cities near Raleigh, NC with the most Every Cure job openings:

Every Cure jobs near you
Infographic showing various Every Cure job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 74% Full Time, 20% Part Time, and 5% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $55,763 per year, or $26.8 per hour.

Pharmacovigilance Specialist - US - Remote

Worldwide Clinical Trials

Durham, NC • Remote

Full-time

Re-posted 7 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 Associate, Pharmacovigilance does at Worldwide

Responsible for the collection, processing, evaluation and reporting of incoming Serious Adverse Event (SAE) data according to applicable regulatory guidelines/requirements, Worldwide Standard Operating Procedures (SOPs) and project specific instructions.

Serves as Lead PV Associate on small to moderate sized studies that are simple to moderate in complexity and scope of work with support from senior staff.

What you will do

  • Author Safety Management Plan for assigned studies
  • Review incoming SAE data for completeness and accuracy
  • Perform data entry in the Safety Database and/or complete applicable tracking of incoming safety information
  • Generate queries for missing or unclear information and follow-up with sites for resolution
  • Perform QC of SAEs processed by other PV Associates
  • Generate regulatory reports and perform safety submissions as needed

What you will bring to the role

  • Good understanding of medical and scientific terminology, of the principles of clinical assessment of adverse drug events, of international regulations and of reporting requirements
  • Good understanding of computer technology, and management of relational database systems, including extraction of data
  • Positive attitude and ability to interact diplomatically and professionally with internal and external customers in a global environment
  • Excellent organization skills and ability to handle multiple competing priorities within tight timelines
  • Consistently demonstrates commitment, dependability, cooperation, adaptability and flexibility in executing daily tasks and responsibilities
  • Ability to anticipate needs and follow through on all assigned tasks

Your experience

  • Bachelor's degree in a science-related field, nursing, or equivalent
  • Minimum of 1 year of pharmacovigilance experience (pre-approval clinical trials)
  • Equivalent combination of relevant education and experience
  • Computer literacy and strong working knowledge of MS Office applications (Excel, PowerPoint, Word)
  • Excellent written and verbal communication skills
  • Excellent organization skills and attention to detail
  • Demonstrated ability to handle multiple competing priorities while adhering to applicable timelines
  • Ability to work independently, prioritize work effectively and work successfully in matrix team environment
  • Ability and willingness for potential limited travel (domestic and international) as needed (attend Investigator Meeting, project kick-off meeting and/or bid defense meeting)
  • Fluent in written and verbal English

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 - $50,000.00 - $99,000.00


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.

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