The Global Study Manager (GSM) is a member of the extended global study team supporting the delivery of clinical studies within BioPharmaceuticals Clinical Operations. The GSM is responsible for supporting study manageme…
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…
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…
As a member of IQVIA’s Identity and Access Management (IAM) team, the Security Program Manager will be responsible for gathering, analyzing, and managing requirements that support the delivery of IQVIA’s enterprise infor…
Job Overview Senior Clinical Leads are an integral part of clinical trial delivery, leading and working alongside clinical teams to improve patients’ lives by bringing new drugs to the market faster. The Senior Clinical …
Skills: Clinical trial delivery, Project management, Good Clinical Practice (GCP), International Conference on Harmonization (ICH), Risk mitigation
Clorox is the place that’s committed to growth – for our people and our brands. Guided by our purpose and values, and with people at the center of everything we do, we believe every one of us can make a positive impact o…
Skills: Category management, Team leadership, Talent development, Strategic planning, Data analysis
Licensed Clinical Social Worker Supervisor - Outpatient (LCSW, LCMHC, LMFT)
Durham, North Carolina, United States · Hybrid
$70k–$115k/yr
Senior$410M raised
At LifeStance Health, we believe in a truly healthy society where mental and physical healthcare are unified to make lives better. Our mission is to help people lead healthier, more fulfilling lives by improving access t…
Skills: Clinical supervision, Mental health therapy, Patient care, Behavioral health, Outpatient care
Anticipated End Date: 2026-10-02 Position Title: Medical Director Associate – CarelonRx Job Description: Medical Director Associate – CarelonRx Location: This role enables associates to work virtually full-time, with the…
Associate Benefits: Work-life balance Training Employee Discount Paid time off Tuition Reimbursement Employee Assistance Program (EAP) This position is eligible for company benefits including but not limited to medical, …
Skills: Sales management, Client relationship management, KPI analysis, Team leadership, Staff training
We are the people who give possibilities purpose BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination …
Be You. Be Bold. Choose Duke. Assistant Supervisor, Environmental Services Be You. At Duke, we celebrate individuality and the unique perspectives that each member of our community brings. As the Assistant Supervisor, En…
Build a career helping local families protect what matters most. Alchemy Financial Group is hiring motivated people for a field-based life insurance sales opportunity in your local area. Previous insurance experience is …
Skills: Life Insurance Sales, Field Coaching, Client Relationship Management, Communication, Follow-up
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…
We’re building a world of health around every individual — shaping a more connected, convenient and compassionate health experience. At CVS Health®, you’ll be surrounded by passionate colleagues who care deeply, innovate…
With nearly 20,000 global hires and more than one million applications annually, attracting top talent is critical to IQVIA’s success. Behind every application is a journey shaped by meaningful interactions that help can…
Clorox is the place that’s committed to growth – for our people and our brands. Guided by our purpose and values, and with people at the center of everything we do, we believe every one of us can make a positive impact o…
Board Certified Behavior Analyst (BCBA) with Relocation Assistance
Durham, North Carolina, United States · Hybrid
$80k–$96k/yr
Mid level
Description We are looking for a leader and an experienced Behavior analyst to join our ABA program in an established multi-disciplinary clinic. Requirements Qualities that fit this opportunity Minimum of 3 years of expe…
Skills: Behavior analysis, Comprehensive intervention development, Supervision, Mentoring, Team leadership
Description We are looking for a leader and an experienced Behavior analyst to join our ABA program in an established multi-disciplinary clinic. Due to state billing requirements, candidates for this remote position must…
Skills: Behavior analysis, Aba program development, Parent training, Supervision, Mentoring
Qualified Behavior Analyst (QBA) with Relocation Assistance
Durham, North Carolina, United States · Hybrid
$80k–$96k/yr
Mid level
Description We are looking for a leader and an experienced Behavior Analyst to join our ABA program in an established multi-disciplinary clinic. Requirements Qualities that fit this opportunity Minimum of 3 years of expe…
Skills: Applied behavior analysis, Intervention development, Supervision, Mentoring, Team leadership
Williams-Sonoma, Inc.
Lead Sales (Key Holder) FT Pottery Barn Southpoint Durham
Durham, North Carolina, United States · On-site
Entry level$4M raised
We hope you're interested in building a home with us. Even if you don't feel that you meet every requirement listed in this job description, we still encourage you to apply. About the Team Our mission is to enhance the q…
Sign up with Clera and we'll reach out the moment a role actually fits you — no more spraying applications into the void.
$120k–$181k/yr
Full-time
bachelor degree, postgraduate degree
Competitive base salary, Annual bonus, Long-term incentives, Paid time off, Health benefits, Medical coverage
Posted 2d ago
Apply by Sep 25
~40 hrs/week
Responsibilities
The Global Study Manager supports the delivery of clinical studies by coordinating cross-functional teams, managing CROs, and ensuring adherence to timelines, budgets, and quality standards. They are responsible for study documentation, risk mitigation, and maintaining inspection readiness throughout the clinical study lifecycle.
Requirements
Candidates must hold a bachelor's degree in a life sciences discipline and possess at least 3 years of relevant experience in the pharmaceutical or clinical research industry. A strong understanding of ICH-GCP regulations, clinical development processes, and demonstrated project management capabilities are required.
Full job description
The Global Study Manager (GSM) is a member of the extended global study team supporting the delivery of clinical studies within BioPharmaceuticals Clinical Operations. The GSM is responsible for supporting study management activities to ensure delivery to agreed timelines, budget, and quality standards, from Clinical Study Protocol (CSP) development through study start-up, maintenance, close-out, Clinical Study Report (CSR) development, and study archiving.
The GSM partners cross-functionally with internal and external stakeholders to execute delegated aspects of clinical studies in accordance with the direction of the Global Study Director (GSD) or Global Study Associate Director (GSAD). The role ensures compliance with AstraZeneca's Delivery Model, Project Management Framework, applicable regulations including ICH GCP, company SOPs, policies, guidelines, values, and behaviors.
Key Responsibilities
Partner with internal clinical teams, subject matter experts, CROs, and external service providers to ensure successful study delivery.
Lead and contribute to preparation of study documents, including informed consent forms, master clinical study agreements, study-specific procedures, specifications, presentations, and other required documents.
Coordinate and facilitate interactions between internal functions, CROs, and external vendors to support efficient study execution within timeline, budget, and quality expectations.
Support the planning and execution of internal and external meetings, including investigator and monitor meetings.
Ensure investigational product and study material supply through collaboration with Clinical Supply Chain and external partners.
Identify study risks and issues proactively and contribute to mitigation and action plans.
Ensure study-related documentation within assigned scope is complete, accurate, and maintained in the Trial Master File (TMF).
Support budget management activities, including invoice reconciliation and vendor financial tracking.
Adhere to global clinical processes, Quality & Compliance requirements, and international regulations to ensure inspection readiness at all times.
Provide project management support to the GSD and/or GSAD as delegated.
Support management and oversight of CRO Project Managers for outsourced studies, ensuring delivery against agreed timelines, budgets, and quality standards while maintaining appropriate documented oversight.
Participate in process improvement initiatives and lead non-drug project work as assigned.
Education and Qualifications
Required
Bachelor's degree in medical, Biological, Life Sciences, or a related clinical research discipline.
Minimum of 3 years of relevant experience within the pharmaceutical industry, contract research organization, biotechnology company, or academic clinical research environment.
Knowledge of clinical development and drug development processes across multiple phases and therapeutic areas.
Strong understanding of ICH-GCP and global clinical trial regulations.
Excellent communication, collaboration, and stakeholder management skills.
Experience managing external service providers and/or CROs.
Demonstrated project management skills.
Ability to work effectively both independently and within cross-functional teams.
Demonstrated leadership and problem-solving capabilities.
Strong computer proficiency and experience using clinical systems and business applications.
Excellent written and verbal communication skills in English.
Preferred
Advanced degree (Master's, PharmD, PhD, or equivalent).
Experience across the full clinical study lifecycle from start-up through close-out.
Knowledge of additional GxP areas, including GMP and GLP.
Experience supporting global clinical studies and outsourced delivery models.
People Management
No direct reports.
May provide matrix leadership and study team coordination across internal and external stakeholders.
Functional Skills
Clinical Trial Management
Clinical Operations
GCP / ICH Compliance
Vendor Management
CRO Oversight
Study Documentation Management
Trial Master File (TMF) Management
Risk Management
Budget Tracking and Reconciliation
Cross-Functional Collaboration
Project Management
Stakeholder Management
Why AstraZeneca:
Here, your start-up leadership shapes the path from promising data to approved medicines. You will work on assets at different stages, influence strategy early, and collaborate with experts who bring science, operations, and technology together in the same room to unlock faster decisions. We balance bold ambition with genuine support, valuing kindness alongside drive, and encourage you to question, experiment, and harness new tools that shorten development cycles and amplify patient impact.
Step into a role where your expertise activates studies faster and strengthens approvals—bring your start-up leadership to AstraZeneca and create momentum that matters now!
Benefits
We offer a competitive Total Reward program, including:
· Competitive base salary, annual bonus, and long-term incentives
· Generous paid time off program
· Comprehensive benefits package
Diversity and Inclusion at AstraZeneca AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive team that represents a diverse group of backgrounds and perspectives, knowing that inclusion drives better outcomes.We welcome all qualified candidates and align with applicable laws regarding inclusivity and employment eligibility. Individuals with disabilities can request reasonable accommodations during the application or interview process, as well as for essential job functions.
The annual base pay (or hourly rate of compensation) for this position ranges from $120,355.20 - $180,522.80 USD Annual, either as annual base pay or as the hourly rate (annual base pay divided by 2080 hours)]. Hourly and salaried non-exempt employees will also be paid overtime pay when working qualifying overtime hours. Base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles). Benefits offered included a qualified retirement program [401(k) plan]; paid vacation and holidays; paid leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base pay (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.
Date Posted
10-Sep-2026
Closing Date
24-Sep-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.
Related keywords
Clinical Study ManagerBioPharmaceuticalsClinical OperationsClinical Study ProtocolClinical Study ReportICH GCPSOPCROTrial Master FileTMFBudget ManagementVendor Financial TrackingInspection ReadinessClinical Supply ChainLife SciencesDrug Development
We're transforming the future of healthcare by unlocking the power of what science can do for people, society and the planet. For more information, visit www.astrazeneca.com.
Community Guidelines: bit.ly/2MgAcio
Offices: 1 Francis Crick Avenue, Cambridge Biomedical Campus, Cambridge, Cambridgeshire CB2 0AA, GB · Astraallen, Sodertalje, Stockholm County 152 57, SE
PharmaceuticalBiopharmaceuticalInnovationResearch and developmentand Global businessHealth CareBiopharmaLife ScienceBiotechnologyMedical
How much do Management & Leadership jobs in Durham, NC pay?
Based on 696 listings with disclosed salaries, most management & leadership jobs in Durham, NC pay between $50k–$225k per year. Individual offers vary with seniority, company size, and specialization.
How many Management & Leadership jobs are open in Durham, NC right now?
There are currently 1,542 open management & leadership positions in Durham, NC listed on Clera. New openings are added daily as companies post roles.
Which companies are hiring for Management & Leadership roles in Durham, NC?
Companies currently hiring include Duke University School of Medicine, IQVIA, Duke University Hospital, Fidelity Investments, NetApp, among others. Browse the listings above to see every active employer.
Are there remote or hybrid Management & Leadership jobs in Durham, NC?
Yes — 433 of the 1542 open management & leadership positions offer remote or hybrid work (146 remote, 287 hybrid).
How do I apply for Management & Leadership jobs in Durham, NC?
Each listing links directly to the employer's application page. Apply early — fresh listings get the most recruiter attention in the first two weeks.