Welcome to PacePharm!

We’re delighted to welcome you to our consultancy dedicated to empowering professionals in the fast-paced realms of clinical research and pharmaceutical management.

  • Project management

  • Investigational Site Monitoring Services

  • Clinical Research Support Services

  • Interview Assistance

  • On-the-Job Support

Jimmy Lewis

Senior Consultant

Project management

At Pace Pharm, we recognize that effective project management is paramount to the success of clinical trials. Our dedicated team of project managers brings unparalleled expertise and commitment to every project, ensuring seamless execution and timely delivery of results. With a focus on precision, efficiency, and innovation, we empower our clients to navigate the complexities of clinical research with confidence and ease.

Why Choose Pace Pharm for Project Management?

Expertise

Our project managers are seasoned professionals with extensive experience in clinical research and project management.

Tailored Solutions

We collaborate closely with our clients to develop customized project management strategies that align perfectly with their goals and timelines.

Compliance and Integrity

Upholding the highest standards of integrity and compliance is non-negotiable for us.

Innovation and Efficiency

We believe in the power of innovation to drive progress and efficiency. By leveraging cutting-edge tools and methodologies, our project managers streamline processes and optimize resources.

Our Comprehensive Project Management Services Include

Risk Management

Our project managers employ robust risk management strategies to anticipate potential challenges and proactively address them, minimizing disruptions and ensuring project success.

Stakeholder Communication

Our project managers serve as the central point of contact for all stakeholders, facilitating clear and transparent communication to keep everyone informed and aligned throughout the project lifecycle.

Quality Assurance

Our project managers implement rigorous quality assurance measures to ensure that all activities meet regulatory requirements and industry standards, safeguarding the integrity of the data and the well-being of study participants.

Performance Monitoring and Reporting

Our project managers monitor project performance closely, tracking key metrics and milestones to provide timely insights and actionable recommendations to our clients.

Ready to Elevate Your Clinical Trials with Pace Pharm Project Management Services?

Partner with Pace Pharm today and experience the difference that expert project management can make in your clinical research endeavors. Contact us now to learn more and schedule a consultation with our experienced team. Together, let’s unlock the full potential of your projects and drive success in the ever-evolving world of healthcare and life sciences.

Investigational Site Monitoring Services

Investigational Site Monitoring is a crucial aspect of any Clinical Trial. Our professional CRAs, Lead CRAs and CTAs can manage all of your site visits, such as Pre-study (PSV), Site initiation (SIV), interim monitoring (IMV) and close-out (COV) visits. Trust our team to monitor your clinical trials.

Clinical Monitoring Services 

Our Clinical Monitoring Services are designed to provide comprehensive oversight at every stage of the trial, delivering timely and detailed reports to our clients after each monitoring service.

Pre-Study / Qualification Visit

Our expert team evaluates the capabilities of site staff, adherence to FDA regulations and Good Clinical Practices (GCPs), and overall readiness to conduct the trial effectively and ethically.

Close-Out Visit

Upon completion of the clinical trial, Pace Pharm orchestrates meticulous close-out visits to finalize all aspects of the study.

Clinical Monitoring Initiation Visit

Once a trial is initiated, Pace Pharm facilitates a seamless start by conducting comprehensive initiation visits at research sites.

Interim Clinical Monitoring Visit

Throughout the duration of the trial, Pace Pharm conducts ongoing monitoring visits to ensure quality and compliance.

Clinical Research Support Services

Our comprehensive support services are tailored to meet the unique needs of clinical research professionals, providing the tools, guidance, and assistance necessary to navigate the complexities of their roles effectively.

Training and Education

Our training programs cater to a wide range of clinical research professionals, providing thorough education in Good Clinical Practice (GCP) guidelines, regulatory requirements, study protocols, and specialized procedures. Continuous learning opportunities ensure professionals stay updated on industry standards and best practices.

We provide easy access to essential resources such as study protocols, case report forms (CRFs), investigator brochures, and regulatory documents. Accessible resources enable professionals to perform their duties efficiently and maintain data integrity throughout the trial process.

Our technical support team assists professionals in navigating various software and tools used for data collection, monitoring, and reporting. Whether troubleshooting issues or mastering new technologies, we ensure professionals have the technical support they need to excel in their roles.

Effective communication is essential for professionals to interact with study sites, sponsors, and stakeholders. We offer support in developing strong communication skills, addressing concerns, and resolving discrepancies promptly and professionally.

With professionals often juggling multiple tasks and deadlines, effective time management is crucial. Our support services include guidance on workload management, task prioritization, and meeting deadlines to optimize efficiency and productivity.

Professionals encounter various challenges during clinical trials, from protocol deviations to data discrepancies. We provide support in honing problem-solving skills, enabling individuals to address issues effectively while maintaining compliance with regulations and protocols.

Ensuring data accuracy, protocol adherence, and regulatory compliance is paramount in clinical research. Our support services encompass conducting quality assurance checks, identifying compliance issues, and implementing corrective actions to uphold the highest standards of quality and integrity.

We understand the demanding nature of clinical research and the toll it can take on professionals. To provide holistic support, we offer access to resources for emotional well-being, including counseling services and peer support groups, to help individuals manage stress and cope with the challenges of their work.

Our support services ensure that professionals can conduct thorough and timely Source Data Verification (SDV) and Source Data Review (SDR) while adhering to study protocols, optimizing data quality and integrity throughout the trial process.

We offer comprehensive training and development programs tailored to the needs of clinical research professionals, enhancing their skills and knowledge to excel in their roles.

Professionals can rely on our support in facilitating the recruitment of qualified investigators for clinical trials through targeted outreach and engagement efforts.

We provide expertise and guidance in negotiating budgets and contracts with sites, vendors, and other stakeholders, ensuring fair and favorable terms for all parties involved.

Our support services encompass the development of risk management plans to proactively identify, assess, and mitigate risks associated with clinical trials, ensuring the successful execution of trials while minimizing potential risks.

Site Communication

Our support services facilitate effective communication with investigative sites, sponsors, and stakeholders, enabling professionals to address queries, resolve issues, and provide necessary support to ensure trial success.

Professionals can rely on our assistance in creating clear and concise presentation slides for study team meetings, investigator meetings, and regulatory submissions, facilitating effective communication and collaboration.

We provide support in developing compelling resumes that showcase professionals’ skills, experience, and accomplishments, helping them stand out to potential employers in the competitive clinical research industry.

Our guidance and resources empower professionals to utilize online platforms effectively for job search, networking, and career advancement, maximizing their opportunities for career growth and development.

We offer assistance in preparing and delivering engaging and informative Site Initiation Visit (SIV) presentations, ensuring that site staff understand study protocols, procedures, and expectations clearly and comprehensively.

We provide guidance and resources to support professionals in preparing for investigator meetings, facilitating seamless communication and collaboration between study teams and investigators.

Professionals can rely on our assistance in effectively interacting with data management teams, ensuring accurate and timely data collection, entry, and validation to maintain data integrity.

Our support services offer insights and strategies for optimizing clinical operations and ensuring global compliance and conduct standards are met, facilitating the successful execution of multinational clinical trials.

We assist professionals in organizing, preparing, and managing regulatory documents to ensure compliance with regulatory requirements throughout the trial process.

Our support services include guidance and resources to support professionals in the site selection and qualification process, ensuring the selection of qualified sites capable of meeting study requirements and regulatory standards.

We conduct quality control audits to assess compliance with study protocols, regulatory requirements, and quality standards, ensuring the integrity and reliability of trial data.

Our support services include strategies for continuous process improvement to enhance efficiency, reduce costs, and improve overall trial outcomes.

We provide guidance and assistance during the post-trial phase, including data analysis, results dissemination, and regulatory reporting, ensuring a smooth transition from trial completion to post-trial activities.

Interview Assistance

Comprehensive Training

Access our extensive training modules covering all facets of clinical research, including Good Clinical Practice (GCP) guidelines, regulatory requirements, study protocols, and specialized procedures, meticulously designed by industry experts.

Personalized Interview Preparation

Receive tailored support for interview preparation, including mock interviews, constructive feedback sessions, and guidance on presenting your skills and experience with confidence and clarity, ensuring you stand out in competitive job interviews.

Career Enhancement

Ideal for professionals aspiring to elevate their skills and secure new opportunities within the dynamic field of clinical research, Pace Pharm’s training equips you with the knowledge and confidence to excel in your career journey.

Competitive Pricing

Benefit from competitive pricing for our training packages, ensuring exceptional value without compromising on quality or effectiveness, making professional development accessible and affordable.

Additional Resources for Success

Unlock access to supplementary resources such as resume building assistance, networking strategies, and job search optimization techniques provided by Pace Pharm’s experts, empowering you to maximize your potential for success in the competitive job market.

On-the-Job Support

Advanced Training Excellence

Immerse yourself in Pace Pharm’s advanced training modules meticulously crafted by industry experts, featuring immersive exercises and real-world case studies to deepen your understanding and enhance your skills.

Expert On-the-Job Support

Receive unparalleled guidance and support from seasoned industry professionals at Pace Pharm, dedicated to empowering you with practical insights, answering your queries, and guiding you towards excellence in your clinical research role.

Practical Hands-On Experience

Tailored for professionals seeking immersive hands-on experience and actionable guidance to excel in their clinical research roles from day one, Pace Pharm’s training with on-the-job support ensures you are well-equipped for success.

Customizable Career Plans

Customize your training journey at Pace Pharm to align with your unique career aspirations and development goals, with flexible options to focus on areas of interest and priority, ensuring personalized and impactful professional growth.

Industry-Leading Mentorship

Benefit from the mentorship and expertise of seasoned professionals at Pace Pharm committed to nurturing your talents and empowering you to thrive in the challenging yet rewarding landscape of clinical research.

PACE PHARM FAQ

Is the Pace Pharm Clinical Research program certified?

In contrast to numerous healthcare professions, Clinical Research does not mandate certification for entry. While you can pursue certification after two years of active experience, initial involvement and skill development only necessitate training in core clinical trial competencies. The Pace Pharm Clinical Research program is designed to cater to individuals with varying levels of experience in Clinical Research. Whether you have limited knowledge of clinical research or are seeking mentorship to enhance your success in the field, our program provides comprehensive training in core competencies and offers industry-focused career coaching. Additionally, participants receive access to our network of Clinical Research connections and institutions, further supporting their professional development and success in the field.

Clinical Research involves the investigation of new medical treatments, drugs, or devices through carefully controlled trials conducted with human participants. Professionals in this field, including Clinical Research Associates (CRAs), Clinical Research Coordinators (CRCs), Quality Assurance (QA) specialists, and more, play crucial roles in ensuring the safety, efficacy, and integrity of these trials.

To pursue a career in Clinical Research, individuals need specialized training, qualifications, and hands-on experience. Pace Pharm’s Clinical Research program offers comprehensive training tailored to aspiring professionals seeking to enter the field. Our program covers essential topics such as good clinical practice (GCP) guidelines, regulatory requirements, data management, and more.

Through our industry-focused curriculum and practical experience, graduates of our program are equipped with the necessary knowledge and skills to excel in various roles within Clinical Research, including CRA positions. Join Pace Pharm’s Clinical Research program and embark on a rewarding career path in this dynamic and impactful field.

Absolutely! At Pace Pharm, we’re dedicated to guiding our students towards fulfilling career opportunities in Clinical Research. Each student is paired with a dedicated career mentor who provides personalized support in resume refinement, interview preparation, and networking strategies. Our expert instructors and guest speakers offer invaluable insights into the industry, equipping students with the knowledge and skills needed to excel in their careers.

But our commitment doesn’t end there! Even after classes conclude, our directors continue to work closely with students, assisting them in identifying suitable job openings aligned with their skills and aspirations. From honing interview techniques to crafting professional resumes and building strong networks, we’re with our students every step of the way.

Our mission is simple yet profound: to empower talented and driven individuals like you to embark on rewarding careers and make meaningful contributions to clinical trials. Join us at Pace Pharm, where your journey towards a fulfilling career in Clinical Research begins!

Our comprehensive training program at Pace Pharm spans a duration of 10 weeks. This intensive period equips participants with the essential knowledge, skills, and hands-on experience needed to excel in the field of Clinical Research. Led by industry experts and seasoned professionals, our 10-week program is carefully crafted to provide a dynamic and immersive learning experience. From mastering core competencies to gaining valuable insights into industry trends, our training ensures that participants are well-prepared to embark on rewarding careers in Clinical Research. Join us at Pace Pharm and kickstart your journey towards a successful and fulfilling career today!

At Pace Pharm, we believe in offering more than just a training program; we provide a transformative experience that sets our participants apart in the competitive field of Clinical Research. Here’s why choosing Pace Pharm is the best decision for your career:

  • Comprehensive Curriculum: Our program offers a comprehensive curriculum designed by industry experts to cover all aspects of Clinical Research, ensuring that you receive the most relevant and up-to-date training available.
  • Hands-On Experience: From day one, you’ll dive into real-world scenarios and hands-on projects that simulate the challenges and opportunities you’ll encounter in your future career, providing invaluable practical experience.
  • Expert Instructors: Learn from the best in the industry! Our instructors are seasoned professionals with years of experience in Clinical Research, offering invaluable insights, mentorship, and guidance throughout your journey.
  • Career Support: We’re invested in your success. From resume building to interview preparation and job placement assistance, our dedicated career support team is here to help you every step of the way, ensuring that you’re well-equipped to land your dream job in Clinical Research.
  • Cutting-Edge Resources: Access to industry-leading resources ensures that you’re equipped with the tools and knowledge needed to thrive in today’s competitive job market.
  • Networking Opportunities: Connect with industry professionals, alumni, and peers through our extensive network of Clinical Research connections and events, opening doors to exciting career opportunities and collaborations.
  • Flexibility: Our program offers flexible scheduling options to accommodate your busy lifestyle, allowing you to pursue your passion for Clinical Research without compromising your other commitments.

While having a healthcare background can be advantageous, it’s not a strict requirement. At Pace Pharm, we’ve seen numerous successful professionals enter the field of clinical research from diverse backgrounds, including social sciences and fine arts. The clinical research industry values diversity and welcomes individuals from various disciplines.

What matters most are the qualities that you bring to the table: a strong work ethic, attention to detail, and a genuine passion for making a difference in people’s lives. These attributes, combined with our comprehensive training and support, can pave the way for a rewarding career in Clinical Research.

At Pace Pharm, we welcome individuals with diverse educational backgrounds and experiences to apply for our training program in Clinical Research. While specific qualifications may vary depending on the program, we generally look for candidates who possess a strong desire to learn and succeed in the field of Clinical Research. A bachelor’s degree in a relevant field such as life sciences, health sciences, pharmacy, nursing, or a related discipline is preferred but not always required. Additionally, having a solid understanding of scientific principles, strong communication skills, attention to detail, and a passion for contributing to medical advancements are qualities we value in our applicants. Ultimately, we assess each candidate holistically to ensure they have the potential to thrive in our program and make meaningful contributions to the field of Clinical Research.