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GlaxoSmithKline Clinical Trial Manager Resume Examples

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Brenna Goyette
Certified Professional Resume Writer, Career Expert

Published 8 min read

This article guides applicants on crafting a compelling resume for a Clinical Trial Manager position at GlaxoSmithKline. It emphasizes showcasing expertise in clinical research, project management skills, and a solid understanding of regulatory standards. Tips include highlighting achievements in trial management, demonstrating leadership in cross-functional teams, and illustrating proficiency in data analysis and patient safety protocols to stand out in the competitive pharmaceutical industry.

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Clinical Trial Manager Resume Example (Text)

Onika Peachee, Clinical Trial Manager


(274) 265-3622

Concord, NH

Professional Summary

A dedicated Clinical Trial Manager with 5 years of experience in planning, executing, and overseeing clinical trials in a variety of therapeutic areas. Expert in navigating regulatory requirements, managing cross-functional teams, and ensuring trials are conducted in accordance with protocol, budget, and timelines. Demonstrated ability to collaborate with investigators, site personnel, and internal stakeholders to achieve trial objectives. Skilled in data analysis, problem-solving, and adapting to evolving trial landscapes. Proven track record in improving processes, enhancing patient recruitment strategies, and maintaining high standards of compliance and ethics. Committed to advancing medical research and contributing to the development of innovative healthcare solutions.

Work Experience

Clinical Trial Manager at Novo Nordisk, NH

Jan 2024 - Present

  • Streamlined Patient Recruitment Process**: Successfully revamped the patient recruitment strategy for a Phase III diabetes trial, reducing recruitment timelines by 30%. This involved implementing a digital outreach program and establishing partnerships with local clinics, directly resulting in the on-time enrollment of 250+ participants.
  • Efficiency in Trial Management**: Spearheaded the management of a global, multi-center clinical trial involving over 500 patients across 10 countries, completing the trial 3 months ahead of schedule. Implemented innovative project management techniques and leveraged technology for better coordination among international teams, which significantly improved efficiency and reduced operational costs by 15%.
  • Data Integrity and Compliance Enhancement**: Led a cross-functional team to enhance data integrity and compliance, achieving a 98% compliance rate with FDA regulations and Good Clinical Practice (GCP) standards. This was accomplished through the development of rigorous training programs for study personnel and the introduction of advanced data monitoring tools, ensuring high-quality data collection and reporting.
  • Publication Success**: Directed research that led to the publication of findings from a critical phase II trial on a novel insulin therapy in "The New England Journal of Medicine". The study's outcomes contributed to advancing scientific understanding of treatment options for type 1 diabetes and garnered significant attention from the medical community, enhancing Novo Nordisk's reputation in endocrinology research.

Associate Clinical Trial Manager at Pfizer, NH

Aug 2019 - Dec 2023

  • Oversaw and successfully managed the execution of a Phase III clinical trial for a groundbreaking oncology drug, completing the study 2 months ahead of schedule by implementing innovative patient recruitment strategies that increased enrollment rates by 30%.
  • Led a cross-functional team of 20+ members, including data managers, clinical research associates, and biostatisticians, in the seamless transition to a fully remote monitoring system amidst the COVID-19 pandemic, ensuring zero disruptions in trial timelines and maintaining 100% compliance with FDA regulations.
  • Spearheaded the development and implementation of an improved patient data collection protocol which reduced data discrepancies by 40%, significantly enhancing the accuracy and reliability of trial outcomes and contributing to the expedited approval process for two key medications.


Master of Science in Clinical Research at Dartmouth College, NH

Oct 2015 - May 2019

Relevant Coursework: Biostatistics, Clinical Trial Design, Epidemiology, Regulatory Affairs, Ethical Issues in Clinical Research, Data Management and Informatics, Health Economics, and Patient-Centered Outcomes Research.


  • Project Management
  • Regulatory Compliance
  • Data Analysis
  • Risk Management
  • Patient Recruitment
  • Budget Oversight
  • EDC Systems


  • Certified Clinical Research Professional (CCRP) - Offered by the Society of Clinical Research Associates (SOCRA), this certification is designed for clinical research professionals who have a broad-based understanding and experience in clinical trial management.
  • Association of Clinical

Tips for Writing a Better GlaxoSmithKline Clinical Trial Manager Resume

Crafting a resume for a Clinical Trial Manager position at GlaxoSmithKline (GSK) requires a careful balance of showcasing your scientific expertise, project management skills, and your ability to work within regulatory frameworks. GSK, being a global healthcare leader, looks for candidates who not only have the technical capabilities but also the soft skills to manage diverse teams and drive innovation. Here are some tips to help you write a standout resume for a Clinical Trial Manager role at GSK:

1. Tailor Your Resume to the Job Description

  • Match Keywords: Read the job description carefully and include keywords and phrases in your resume. This shows that you have the specific skills GSK is looking for.
  • Emphasize Relevant Experience: Highlight your experience in clinical trial management, especially if you have worked in areas relevant to GSK’s research interests.

2. Highlight Your Scientific and Regulatory Knowledge

  • Showcase Your Expertise: Detail your understanding of clinical trial phases, regulatory requirements, and Good Clinical Practice (GCP).
  • Certifications and Training: Include any relevant certifications such as Certified Clinical Research Professional (CCRP) or Project Management Professional (PMP).

3. Demonstrate Project Management Skills

  • Quantify Achievements: Use numbers to demonstrate your achievements. For example, mention the number of clinical trials you have managed, the size of teams you have led, or any efficiencies you have introduced.
  • Problem-Solving Abilities: Give examples of challenges you’ve faced in clinical trials and how you overcame them.

4. Showcase Leadership and Communication Skills

  • Team Leadership: Highlight your experience in leading cross-functional teams, including coordinating with researchers, statisticians, and regulatory affairs specialists.
  • Stakeholder Engagement: Mention your skills in working with external stakeholders, such as clinical sites and patient advocacy groups.

5. Detail Your Education and Continuous Learning

  • Advanced Degrees: List your degrees in life sciences, pharmacy, medicine, or related fields. GSK values highly educated candidates.
  • Ongoing Education: Show that you are committed to staying current with the latest in clinical research through courses, seminars, or workshops.

6. Use a Clear, Professional Format

  • Organized Layout: Use bullet points, bold headings, and a clean font to make your resume easy to read.
  • Concise Writing: Be clear and to the point. Your resume should ideally be no longer than two pages.
  • Error-Free: Ensure your resume is free of typos and grammatical errors. This reflects your attention to detail.

7. Include a Cover Letter

  • Personalize Your Application: Write a cover letter that conveys your enthusiasm for the role and explains why you are a good fit for GSK.

Additional Tips:

  • Volunteer Work: If you have volunteered in any capacity that demonstrates your leadership or commitment to healthcare, include this.
  • Professional Memberships: Being part of professional organizations related to clinical research can be an added advantage.

By following these tips, you can create a compelling resume that captures the attention of hiring managers at GlaxoSmithKline. Remember, your resume is not just a list of your past jobs; it’s a tool to showcase your achievements, skills, and potential to contribute to GSK’s mission of helping people to do more, feel better, and live longer.

Related: Clinical Trial Manager Resume Examples

Key Skills Hiring Managers Look for on GlaxoSmithKline Clinical Trial Manager Resumes

Incorporating keywords from the job description when applying for a Clinical Trial Manager position at GlaxoSmithKline (GSK) is crucial due to the company's reliance on Applicant Tracking Systems (ATS). These systems are designed to scan resumes and applications for specific keywords and phrases that match the job description. By carefully integrating these keywords into your application materials, you can significantly increase the chances of your resume passing through the ATS filters and catching the attention of hiring managers. Since GSK is a large, global organization that likely receives a high volume of applications, the use of ATS helps them manage and streamline the hiring process. Therefore, tailoring your resume and cover letter to include relevant keywords and competencies listed in the Clinical Trial Manager job description not only demonstrates your alignment with the specific role but also ensures your application is seen by human eyes, thereby improving your chances of being considered for the position.

Here is a consolidated list of essential skills and critical terms often encountered in applications for clinical trial manager positions at GlaxoSmithKline.

Key Skills and Proficiencies
Clinical Trial DesignProtocol Development
Regulatory CompliancePatient Recruitment Strategies
Data ManagementBudget Management
Team LeadershipRisk Management
GCP (Good Clinical Practice)Project Management
Vendor ManagementClinical Monitoring
Safety MonitoringQuality Assurance
Statistical Analysis UnderstandingCommunication Skills
Ethical ConsiderationsElectronic Data Capture (EDC) Systems
Cross-functional Team CoordinationProblem-solving Skills
Clinical Research EthicsTime Management

Related: Clinical Trial Manager Skills: Definition and Examples

Common Action Verbs for GlaxoSmithKline Clinical Trial Manager Resumes

Crafting a standout resume for a Clinical Trial Manager position at GlaxoSmithKline demands a strategic approach, especially when it comes to selecting the right action verbs. The challenge lies not just in identifying verbs that accurately describe your responsibilities and achievements, but also in varying these verbs to maintain the reader's interest and demonstrate a wide range of skills. Using the same few verbs, such as "managed" or "led," can quickly become repetitive and fail to convey the depth of your experience. Instead, incorporating a diverse array of action verbs can paint a more dynamic and comprehensive picture of your capabilities. For instance, verbs like "orchestrated," "spearheaded," "innovated," and "optimized" can each bring a unique angle to your contributions and successes in clinical trial management. This variation not only keeps the resume engaging but also underscores your multifaceted skill set, making your application more compelling to GlaxoSmithKline's hiring team.

To enhance your competitive advantage, we have curated a selection of impactful action verbs designed to fortify your resume and secure your upcoming interview:

Action Verbs

Related: What does a Clinical Trial Manager do?

Editorial staff

Photo of Brenna Goyette, Editor


Brenna Goyette

Expert Verified

Brenna is a certified professional resume writer, career expert, and the content manager of the ResumeCat team. She has a background in corporate recruiting and human resources and has been writing resumes for over 10 years. Brenna has experience in recruiting for tech, finance, and marketing roles and has a passion for helping people find their dream jobs. She creates expert resources to help job seekers write the best resumes and cover letters, land the job, and succeed in the workplace.

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