Worldwide Clinical TrialsDurham, North Carolina, United States · Remote OK
$86k–$170k/yr
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 ta…
Skills: Site activation, Project management, Clinical research, Regulatory compliance, ICH GCP
Durham, North Carolina, United States · On-site
A Summer Analyst at Triangle Insights Group performs the same role as our full-time Strategy Analysts through an immersive 10-week program. Analyst Interns work closely with Partners, Managers, and Consultants, and will …
Skills: Critical thinking, Market research, Microsoft PowerPoint, Microsoft Excel, Written communication
Durham, North Carolina, United States · Hybrid
School of Medicine Established in 1930, Duke University School of Medicine is the youngest of the nation's top medical schools. Ranked sixth among medical schools in the nation, the School takes pride in being an inclusi…
Skills: Biostatistics, Clinical Research, Leadership, Data Science, SAS
Durham, North Carolina, United States · On-site
At Duke Health, we're driven by a commitment to compassionate care that changes the lives of patients, their loved ones, and the greater community. No matter where your talents lie, join us and discover how we can advanc…
Skills: Radiologic technology, C-arm fluoroscopy, Diagnostic X-ray, Patient positioning, Radiation safety
Durham, North Carolina, United States · On-site
At Duke Health, we're driven by a commitment to compassionate care that changes the lives of patients, their loved ones, and the greater community. No matter where your talents lie, join us and discover how we can advanc…
Skills: Specimen handling, Laboratory testing, Quality control, Quality assurance, Instrumentation calibration
Durham, North Carolina, United States · On-site
At Duke Health, we're driven by a commitment to compassionate care that changes the lives of patients, their loved ones, and the greater community. No matter where your talents lie, join us and discover how we can advanc…
Skills: Clinical Coaching, Evidence-Based Practice, Quality Improvement, Patient Assessment, Interdisciplinary Collaboration
Durham, North Carolina, United States · On-site
This position is on a 2-2-3 shift Day Shift (6am-6pm) The Manufacturing Associate I/II (Manufacturing Associate) is responsible for performing upstream or downstream processing of bulk intermediates and/or bulk drug subs…
Skills: Bioprocessing, Upstream processing, Downstream processing, cGMP, Aseptic processing
Durham, North Carolina, United States · On-site
Job Title: Safety Technician Location: North Carolina (Durham) Schedule: Contract/Temp (Full Time Hours) Start Date: ASAP Hours: 8:00 a.m. to 4:30 p.m. Pay Range: Dependent Upon Experience Role Overview: The Safety Techn…
Skills: Hazardous waste management, Chemical waste segregation, Regulatory compliance, OSHA standards, EPA regulations
Durham, North Carolina, United States · On-site
$46k–$73k/yr
School of Medicine: Established in 1930, Duke University School of Medicine is the youngest of the nation's top medical schools. Ranked sixth among medical schools in the nation, the School takes pride in being an inclus…
Skills: Program coordination, Data analytics, Project management, Strategic planning, Stakeholder engagement
Durham, North Carolina, United States · On-site
$66k–$107k/yr
School of Medicine Established in 1930, Duke University School of Medicine is the youngest of the nation's top medical schools. Ranked sixth among medical schools in the nation, the School takes pride in being an inclusi…
Skills: Clinical nursing, Research coordination, Patient assessment, Medication administration, Regulatory compliance
Durham, North Carolina, United States · On-site
$75k–$189k/yr
Overview: Plan and conduct independent clinical (GCP) audits to assess compliance with regulations, guidelines, and operating procedures. Prepare and distribute reports of findings to supervisor, operations staff, manage…
Skills: GCP Audits, Clinical compliance, Regulatory interpretation, Root Cause Analysis, CAPA
Durham, North Carolina, United States · On-site
At Duke Health, we're driven by a commitment to compassionate care that changes the lives of patients, their loved ones, and the greater community. No matter where your talents lie, join us and discover how we can advanc…
Skills: Laboratory testing, Specimen handling, Quality control, Quality assurance, Instrumentation calibration
Rosemont, Illinois, United States · On-site
$169k–$470k/yr
Role Overview The Global Asset/Commercialization Partner is a senior client leadership role responsible for helping Emerging Biopharma companies successfully navigate the journey from asset development to commercializati…
Skills: Strategic account management, Commercialization strategy, Launch excellence, Market access, Evidence generation
Durham, North Carolina, United States · On-site
$66k–$107k/yr
School of Medicine: Established in 1930, Duke University School of Medicine is the youngest of the nation's top medical schools. Ranked sixth among medical schools in the nation, the School takes pride in being an inclus…
Skills: Clinical research, Oncology nursing, Clinical trial coordination, Patient advocacy, Regulatory compliance
Durham, North Carolina, United States · On-site
JOB SUMMARY The Manufacturing Quality Assurance (MQA) Specialist is responsible for supporting the Manufacturing process and areas as part of a rapidly expanding GMP Contract Manufacturing Organization. MQA Specialists a…
Skills: Quality Assurance, GMP, Batch Record Review, SOP Review, Deviation Triage
Durham, North Carolina, United States · On-site
$98k–$155k/yr
Company Description It started with a simple idea: what if surgery could be less invasive and recovery less painful? Nearly 30 years later, that question still fuels everything we do at Intuitive. As a global leader in r…
Skills: Mechanical Engineering, Biomedical Engineering, Product Development, CAD, Solidworks
Durham, North Carolina, United States · On-site
Quality Assurance Specialist Department: Quality Assurance Employment Type: Full Time Location: Research Triangle Park, NC Description Kriya is a biopharmaceutical company whose mission is to develop life-changing gene t…
Skills: cGMP, Quality Assurance, Batch Record Review, Clinical Labeling, Deviations
Durham, North Carolina, United States · On-site
School of Medicine Established in 1930, Duke University School of Medicine is the youngest of the nation's top medical schools. Ranked sixth among medical schools in the nation, the School takes pride in being an inclusi…
Skills: JAK Inhibitors, Histological Staining, IHC, IF Staining, Cellular Analysis
Durham, North Carolina, United States · On-site
School of Medicine Established in 1930, Duke University School of Medicine is the youngest of the nation's top medical schools. Ranked sixth among medical schools in the nation, the School takes pride in being an inclusi…
Skills: RNA Biology, Epitranscriptomics, Gene Regulation, Functional Genomics, Cell Biology
Durham, North Carolina, United States · Hybrid
$69k–$128k/yr
Duke University: Duke University was created in 1924 through an indenture of trust by James Buchanan Duke. Today, Duke is regarded as one of America’s leading research universities. Located in Durham, North Carolina, Duk…
Skills: Health Policy Research, Quantitative Data Analysis, Qualitative Data Analysis, Policy Writing, Literature Reviews
Worldwide Clinical Trials
Durham, North Carolina, United States • Remote OK
Sign up with Clera and we'll reach out the moment a role actually fits you — no more spraying applications into the void.
The Site Activation Manager is responsible for coordinating and overseeing site identification, essential document collection, and contract status for clinical trials. They ensure all start-up activities are completed on time and within budget while maintaining compliance with GCP and local regulations.
Candidates must have a minimum of a four-year college degree in a life science or related field and at least 4 years of experience in the CRO or pharmaceutical industry. Strong leadership, organizational, and cross-cultural communication skills are required for this role.
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!
*SUMMARY: Accountable for site activation project management and delivery activities within the assigned therapeutic area. Responsibilities include coordination, collaboration and oversight of site identification and central and local ECs (for NA countries only) activities, progression of essential documents collection, monitoring of investigator and site contracts status, and any other country and/or study specific site activation tasks necessary for Site Activation in accordance with Good Clinical Practices (GCPs) and applicable local and international regulations and Standard Operating Procedures (SOPs). May also include pre award support by providing site activation related input into the proposal text and budget items. Reports to a senior member of the Site Activation leadership team within the assigned therapeutic area. RESPONSIBILITIES:* Tasks may include but are not limited to: Serve as the primary point of communication and accountability for study start-up and maintenance (if applicable) activities on assigned projects Oversee project activities of functional groups involved in site activation to ensure critical path activities are completed on-time and within budget Ensure accurate compilation, management, tracking and analysis of site activation activities in a timely manner May support feasibility and/or site identification activities, as needed Work closely with assigned team members to expedite the Site Qualification and Selection process Effectively communicate Site Activation & Regulatory (if applicable) project status to the Sponsor, GPL/CPM and project team Prepare risk assessment and mitigation plans relating to project deliverables with input from other roles Responsible that relevant study activities are present in the work order budget. Ensure OOS activities are tracked and captured within Change Notification Form (CNF) and follow through to execution of change order Work in conjunction with assigned project team members to develop and maintain site activation related project plans May contribute to the development, review, and maintenance of SOPs and best practice guidelines and provide training/coaching pertaining to activities of the Site Activation department Provide input to departmental process improvement initiatives Establish and interpret site activation metrics to help drive corrective action for achieving deliverables, milestones and/or KPIs May participate in business development activities by contributing to proposals and bid defense meetings by preparing relevant sections of proposals, budgets and other country and/or study specific activities related to Site Activation Report and/or escalate issues to Line Manager, Site Activation Portfolio Lead and/or Site Activation Therapeutic Lead to ensure resolution and minimize risks to on-time deliverables Comply with SOPs, ICH GCP and national regulations as applicable Liaise with other functional contributors and vendors as needed Perform other duties as assigned The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive. OTHER SKILLS AND ABILITIES: Strong leadership and organizational management skills in planning, strategizing, managing, monitoring, scheduling, and critiquing Ability to exercise sound judgment and make decisions independently and to proactively identify and solve problems Ability to provide experience and input into initiatives relating to interacting with sites and/or customers Ability to motivate, lead and engage a team Strong interpersonal skills in a fast-paced, deadline oriented, and changing environment Strong oral and written communication skills to clearly and concisely present information Demonstrated ability to collaborate across the business Team-oriented work style; seeks and gives guidance Understanding of regulatory processes and guidelines Understanding of initiation, planning, and execution of clinical projects and overall project planning Awareness of ICH GCP Guidelines and the FDA/EU Clinical Trials Directives/National regulations (CTAs, Amendments, Urgent Safety Measures, End of Trial Notifications) Ability to handle multiple tasks in a fast-paced and constantly changing environment Ability to work in an organized, methodical, and self-motivated manner Proficiency in MS-Office applications including Microsoft Word, Excel, and PowerPoint; digital systems aptitude REQUIREMENTS: A minimum four-year college curriculum with a major concentration in medical, biological, physical, health, pharmacy, or other related science OR two-year college curriculum or equivalent education / training (nursing degree or equivalent life science degree) and experience within clinical research (e.g. CRA, Reg Affairs) Minimum of 4 years CRO/pharmaceutical industry experience, preferably in Start-up Management, Project Management, and/or Site Management experience Proficient in cross-cultural communication Proficient in both spoken and written English Promotion to the next level is not automatic based on years of experience. Personnel are evaluated on proven competency, level of responsibility, and ability to work independently.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):
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.
Worldwide Clinical Trials (Worldwide) is a global CRO serving development-driven biopharmaceutical companies, with more than 4,400 professionals operating across more than 70 countries. The company delivers therapeutically dedicated expertise in neuroscience, oncology, rare disease, and internal medicine, with comprehensive support across every development phase – from early-stage and first-in-human studies through Phase III registration trials. The company's flexible service model – spanning full-service trial management to functional service partnerships through Worldwide Flex – is powered by a people first, partnership driven outsourcing approach that strengthens collaboration, enhances data transparency, and supports more informed decision making. This provides sponsors with tailored, adaptable solutions that keep pace with the evolving demands of clinical research. Learn more at www.worldwide.com
Offices: 600 Park Offices Drive, Suite 200, Research Triangle Park, NC 27709, US · 2455 Northeast Loop 410, Suite 150, San Antonio, TX 78217, US · 4509 Freidrich Lane, Building 2, Suite 200, Southpark Commerce Center Two, Austin, TX 78754, US · 245 First Street Riverview II, Suite 1847, Cambridge, MA 02142, US · 4.1 Manuel Ugarte 2110, CABA, Buenos Aires, 1428, AR
Based on 399 listings with disclosed salaries, most science & research jobs in Durham, NC pay between $55k–$221k per year. Individual offers vary with seniority, company size, and specialization.
There are currently 962 open science & research positions in Durham, NC listed on Clera. New openings are added daily as companies post roles.
Companies currently hiring include Duke University School of Medicine, Duke University Hospital, IQVIA, Duke Health Technology Solutions, KBI Biopharma, among others. Browse the listings above to see every active employer.
Yes — 207 of the 962 open science & research positions offer remote or hybrid work (100 remote, 107 hybrid).
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.
