Jacqueline Imm
Pittsboro,NC
Summary
Highly organized and self-motivated professional experienced in project management, team development and process improvement. Skilled in developing and implementing strategies to increase efficiency and performance. Passionate about driving business growth and creating positive work environment.
Overview
16
16
years of professional experience
Work History
Associate Director, Global Trial Manager
Bristol Myers Squibb
04.2021 - Current
- Proactively identified potential risks and implemented mitigation strategies to minimize negative impacts on projects or business operations.
- Foster culture of continuous improvement by encouraging staff to share innovative ideas and providing resources for professional development.
- Manage internal and CRO resources to achieve 11 country EU CTR submission.
- Drive continuous improvement initiatives across the organization by sharing best practices learned from managing various studies over time.
- Mentor Global Trial Managers, providing guidance on professional development opportunities and career progression paths within the company.
Senior Study Manager
Pfizer (FSP With ExecuPharm)
02.2020 - 04.2021
- Streamlined communication between cross-functional teams, resulting in improved collaboration and timely completion of a Phase III trial in obesity.
- Coordinated with external vendors to optimize resources and ensure seamless integration into the overall study strategy.
- Identified areas of improvement in study processes, leading to increased productivity and cost-effective solutions.
Senior Project Manager
PharPoint Research, Inc.
04.2019 - 01.2020
- Provided outstanding service to clients through effective communication and prompt issue resolution to facilitate future business opportunities.
- Maintained schedules to meet key milestones at every project phase.
- Presented regular status reports to executive leadership, providing insights into progress made toward achieving key milestones.
CRA Manager/ Senior Project Manager
SGS, Clinical (FSP With Brio Resource Group)
10.2018 - 04.2019
- Managed and motivated 5 Lead CRAs and 10 Contract CRAs to be productive and engaged in work.
- Drove operational efficiency through data-driven decision-making processes, leveraging analytics tools for informed strategy development.
- Enhanced customer satisfaction by resolving disputes promptly, maintaining open lines of communication, and ensuring high-quality service delivery.
Senior Study Manager
Merck (FSP With ExecuPharm)
06.2017 - 10.2018
- In-house clinical oversight for multi-center, global, Phase III trial in triple negative breast cancer
- Enhanced study efficiency by implementing effective project management strategies and tools.
- Data management deliverables, protocol level plans/timelines, country/site selection, system updates, Investigator Meeting planning, communication plans, preparation of status update reports, study closeout activities)
- Facilitate and collaborate with key internal/external stakeholders (study team, subsidiary country teams, vendors, committees, etc.) in support of clinical study objectives.
- Monitored study budgets, identifying opportunities for cost savings without compromising on the quality or integrity of research conducted.
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Director, Clinical Operations
Kowa Research Institute
07.2016 - 02.2017
- Developed high-performing teams by providing mentorship, guidance, and opportunities for professional growth.
- Enhanced team collaboration through regular communication, goal setting, and performance evaluations.
- Observed each employee's individual strengths and initiated mentoring program to improve areas of weakness.
- Facilitated cross-functional collaboration for improved decision-making processes within the organization.
Clinical Trial Manager
NantBioScience
11.2015 - 07.2016
- Contributed to protocol development, ensuring a well-designed study that met research objectives while adhering to ethical standards and regulations.
- Developed training materials for site staff to enhance their understanding of the study protocol, resulting in improved adherence to requirements.
- Facilitated clear communication between study teams, vendors, and investigators to maintain alignment on project goals and expectations.
Associate Director, Clinical Trial Services and Manager
United Therapeutics Corporation
11.2013 - 09.2015
- Led teams of up to seven personnel, supervising daily performance as well as training and improvement plans.
- Prioritized tasks and allocated resources appropriately to keep teams focused and productive.
- Assisted senior leadership in managing all aspects of operations.
- Established strong relationships with key industry partners, creating mutually beneficial opportunities for growth and collaboration.
- Assessed risks associated with team activities and implemented appropriate procedures to mitigate potential problems.
Manager, Clinical Sciences
United Therapeutics Corporation
06.2010 - 11.2013
- Accomplished multiple tasks within established timeframes.
- Fostered strong relationships with investigative sites, leading to increased collaboration and improved study outcomes.
- Resolved staff member and site conflicts, actively listening to concerns and finding appropriate middle ground.
- Communicated clearly with employees, vendors, and stakeholders to keep everyone on same page and working toward established business goals.
Clinical Research Manager
Array BioPharma, Inc.
09.2008 - 05.2010
- Coordinated efforts among investigators, sponsors, and regulatory agencies to ensure seamless execution of clinical trials.
- Facilitated training sessions for study staff, enhancing their understanding of protocol requirements and procedures.
- Conducted thorough risk assessments for each project, implementing mitigation strategies where necessary to protect patient safety.
- Complied with research protocols by providing ongoing quality control audits.
Education
BA - Communication Studies
University of Iowa
Skills
- Project Operational Management
- Strategic leadership
- Analytical Thinking
- Coaching and Mentoring
Project Management Experience
- Breast Cancer (Her2 Negative) Phase I
- Type II Diabetes Phase I
- Atopic Dermatitis Phase II
- Advanced Renal Cell Carcinoma Phase II
- Vitiligo Phase II
- Breast Cancer (TNBC) Phase III (Global)
- Epilepsy-Atonic Seizure Phase III (Global)
- Obesity Phase III (Global)
- Obstructive Hypertrophic Cardiomyopathy Phase IIIb/IV (Global)
- Multiple Sclerosis Phase IV (Global)
- Pulmonary Arterial Hypertension Phase IV
References
Available Upon Request
Timeline
Associate Director, Global Trial Manager
Bristol Myers Squibb
04.2021 - Current
Senior Study Manager
Pfizer (FSP With ExecuPharm)
02.2020 - 04.2021
Senior Project Manager
PharPoint Research, Inc.
04.2019 - 01.2020
CRA Manager/ Senior Project Manager
SGS, Clinical (FSP With Brio Resource Group)
10.2018 - 04.2019
Senior Study Manager
Merck (FSP With ExecuPharm)
06.2017 - 10.2018
Director, Clinical Operations
Kowa Research Institute
07.2016 - 02.2017
Clinical Trial Manager
NantBioScience
11.2015 - 07.2016
Associate Director, Clinical Trial Services and Manager
United Therapeutics Corporation
11.2013 - 09.2015
Manager, Clinical Sciences
United Therapeutics Corporation
06.2010 - 11.2013
Clinical Research Manager
Array BioPharma, Inc.
09.2008 - 05.2010
BA - Communication Studies
University of Iowa
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