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Study Com Jobs in Raleigh, NC (NOW HIRING)

MMS

Nonclinical Writer

Raleigh, NC · On-site

Visit www.mmsholdings.com or follow MMS on LinkedIn. This person will participate in the ... Ability to develop a mapping plan for the placement of nonclinical studies within structure of ...

Kapitus

Lead Brand Marketing Coordinator

Raleigh, NC

$41K - $56K/yr

All open positions are posted in location specific employment portals available at www.kapitus.com ... Customer case studies * Testimonial videos * Social media videos * Educational content * Coordinate ...

KBI Biopharma, Inc.

Associate Scientist

Durham, NC · On-site

$76K - $95K/yr

... formulation studies, formulation studies, and clinical in use studies. Responsibilities ... For more information, visit www.kbibiopharma.com. KBI is a proud EEO/AA employer dedicated to ...

Care Access

Region Manager

Raleigh, NC

CareAccess.com. How This Role Makes a Difference We are seeking an experienced and dynamic Region ... Ensure strict adherence to study protocols, IRB/ethics board guidelines, and applicable federal ...

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Showing results 41-60

All JobsStudy Com JobsStudy Com Jobs in Raleigh, NC

Study Com information

See Raleigh, NC salary details

$21.4K

$121.8K

$200.2K

How much do study com jobs pay per year?

As of Aug 6, 2026, the average yearly pay for study com in Raleigh, NC is $121,785.00, according to ZipRecruiter salary data. Most workers in this role earn between $82,600.00 and $152,600.00 per year, depending on experience, location, and employer.

What is the difference between Study Com vs Study Coordinator?

AspectStudy ComStudy Coordinator
Required CredentialsTypically a bachelor's degree, sometimes certifications in clinical researchUsually a bachelor's degree, often with certifications like CCRP or CCRC
Work EnvironmentOffice-based, research institutions, hospitalsClinical settings, hospitals, research sites
Employer & Industry UsageResearch organizations, pharmaceutical companies, academic institutionsHospitals, clinics, research sites
Common Search & ComparisonOften compared for roles in clinical research teamsFrequently compared with Study Com as a supporting role

Study Coordinators and Study Com roles both support clinical research but differ mainly in scope and responsibilities. Study Coordinators typically handle day-to-day trial management, patient coordination, and data collection, while Study Com may focus on broader communication and administrative tasks within research projects. Both roles require relevant certifications and work in similar environments, making them closely related in the clinical research industry.

What are the key skills and qualifications needed to thrive as a study coordinator, and why are they important?

To thrive as a Study Coordinator, you need a solid understanding of clinical research protocols, regulatory compliance, and project management, often supported by a degree in life sciences or healthcare. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certification such as CCRC or CCRP is typically required. Strong organizational skills, attention to detail, and effective communication are crucial soft skills for coordinating between study teams, participants, and regulatory bodies. These competencies ensure studies are conducted ethically, efficiently, and in accordance with regulatory standards, which is vital for research integrity and successful trial outcomes.

What are the typical responsibilities of a study coordinator in a clinical research setting?

A Study Coordinator, often referred to as a Clinical Research Coordinator, is responsible for managing daily operations of clinical trials. This includes recruiting and screening study participants, obtaining informed consent, scheduling and conducting study visits, collecting and recording data, and ensuring compliance with regulatory requirements. Coordinators also act as a liaison between investigators, sponsors, and study participants, making strong organizational and communication skills essential. The role offers opportunities to learn about various aspects of clinical research, paving the way for career advancement into project management or regulatory affairs.

What is a study com?

Study.com jobs refer to employment opportunities with Study.com, an online education platform that provides video lessons, study guides, and other educational resources. Job roles at Study.com can include content writers, curriculum developers, video editors, software engineers, and customer support specialists. Employees work to create and maintain high-quality educational content and ensure a positive learning experience for users. Some positions are remote or freelance, offering flexible work options. Working at Study.com can be a good fit for those passionate about education and technology.
What job categories do people searching Study Com jobs in Raleigh, NC look for? The top searched job categories for Study Com jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Study Com jobs? Cities near Raleigh, NC with the most Study Com job openings:
Study Com jobs near you
Infographic showing various Study Com job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 74% Full Time, 17% Part Time, 1% Temporary, and 7% Contract. Highlights an 94% Physical, 3% Hybrid, and 3% Remote job distribution, with an average salary of $121,785 per year, or $58.6 per hour.

Senior Scientist - Downstream Process Development

Novartis

Durham, NC • On-site

$119K - $222K/yr

Full-time

This job post has expired today. Applications are no longer accepted.

Novartis rating

7.5

Company rating: 7.5 out of 10

Based on 17 frontline employees who took The Breakroom Quiz

64th of 86 rated pharmaceutical

Job description

Job Description Summary

Role type: Full time onsite, #LI-Onsite
Location: Durham, North Carolina, United States
Relocation Support: Yes
Join the team shaping the future of Cell and Gene Therapy and help bring transformational medicines to patients worldwide. As a Senior Scientist - Downstream Process Development, you will play a critical role in advancing viral vector technologies across adeno-associated virus (AAV) and lentiviral vector (LVV) platforms. Combining scientific expertise, innovation, and hands-on laboratory leadership, you will drive process development strategies that support breakthrough therapies from pre-clinical development through clinical manufacturing. This is a unique opportunity to influence cutting-edge science, collaborate with world-class experts, and accelerate the delivery of life-changing treatments to patients with urgent unmet needs.


Job Description

Key Responsibilities

You will serve as the downstream technical lead for one or more gene therapy programs. This role is responsible for defining the overall downstream development plan for assigned gene therapy programs; designing, executing, and interpreting downstream process development studies; performing hands-on process operations at both small scale and large scale; and collaborating with cross-functional teams to advance AAV and LVV programs from pre-clinical development through clinical manufacturing.

Other responsibilities will include:

  • Perform hands-on downstream process operations at both small scale and large scale, delivering high-quality experimental outputs within program timelines.

  • Apply a strong statistical and data-driven mindset to analyze process study results, draw scientifically sound conclusions, and inform development strategy.

  • Drive downstream innovation by evaluating emerging technologies, current scientific advances, and state-of-the-field approaches relevant to viral vector process development.

  • Promote adoption of technical standards, platform approaches, and best practices across multiple programs and modalities.

  • Author technical reports, summarize process development outcomes, and contribute downstream content to regulatory filings, including IND submissions.

  • Present study results, technical recommendations, and development strategies to internal and external stakeholders in cross-functional forums.

  • Be a technical coach and mentor, fostering an innovative, collaborative, and scientifically rigorous culture.

  • Present technical recommendations and mentor colleagues to foster scientific excellence and collaboration.

Essential Requirements

  • Bachelor's degree in biological sciences, pharmaceutical sciences, chemical engineering, or a related technical field with 8+ years of relevant experience; Master's degree with 6+ years of relevant experience; or PhD with 4+ years of relevant experience.

  • Strong technical background in downstream process development for biologics and/or viral vector-based therapies, with hands-on experience designing, executing, and interpreting process development studies.

  • In-depth expertise across multiple downstream unit operations such as chromatography, depth filtration, precipitation or flocculation, tangential flow filtration, ultracentrifugation, impurity clearance, and adventitious virus clearance.

  • Proficiency in statistical analysis principles, Design of Experiments (DoE), and data-driven decision-making.

  • Proven ability to define technical plans, solve complex process development challenges, and deliver scientific objectives within program timelines.

  • Demonstrated ability to influence cross-functional stakeholders, communicate technical recommendations clearly, and contribute to program strategy in a matrixed environment.

  • Innovative mindset with experience advancing continuous improvement, technical standards, best practices, or platform approaches across programs.


EEO Statement:

The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.


Accessibility and reasonable accommodations

The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.


Salary Range

$119,700.00 - $222,300.00


Skills Desired

Data Science, Materials Science, Process Simulation, Technical Writing, Waterfall Model

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