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- Tasks: Join our virtual event to explore CRA opportunities and network with Medpace managers.
- Company: Medpace is a leading clinical research organisation dedicated to developing safe medical therapies.
- Benefits: Enjoy flexible working options, competitive pay, and comprehensive training programs.
- Why this job: Make a real impact in healthcare while growing your career in a supportive environment.
- Qualifications: Must be a CRC or equivalent with a life science degree and right to work in the UK.
- Other info: Selected applicants will receive further details about the virtual event.
The predicted salary is between 28800 - 48000 £ per year.
Job Summary
Medpace is hosting an Entry CRA Networking Event, specifically for Clinical Research Coordinators, where you can meet with Medpace CRA Managers to learn about Clinical Research Associate (CRA) opportunities with Medpace UK.
The Clinical Research Associate (CRA) at Medpace offers the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. For those with medical and/or health/life science interest and background who want to explore the research field and be part of a team bringing pharmaceutical and medical devices to market – this could be the right opportunity for you!
Please note you must be currently working as a CRC, Research Nurse or equivalent, living in the UK with full right to work to be considered. If your application has been selected to attend, further details will be emailed to you prior to the event.
WHEN: Thursday 07th August, PM – exact time TBC.
WHERE: Virtual, Microsoft Teams
WHY MEDPACE?
- London office based positions and fully home based positions available depending on location and experience.
- If office-based, commuting allowance support and travel season ticket loans available.
- Competitive compensation, benefits program and bonus opportunities
- Annual merit increases
- In-House travel agents
- In-Country Managers and Mentors
- Flexible working options
- Extensive training and development available
**More details regarding the format of this virtual event will be provided should you be selected to attend.
Responsibilities
- Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol;
- Communication with the medical site staff including coordinators, clinical research physicians and their site staff;
- Verifying adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;
- Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP and applicable regulatory requirements;
- Verification that the investigator is enrolling only eligible subjects;
- Regulatory document review;
- Medical device and/or investigational product/drug accountability and inventory;
- Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol;
- Assessing the clinical research site\’s patient recruitment and retention success and offering suggestions for improvement;
- Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.
PACE – MEDPACE CRA TRAINING PROGRAM
Medpace provides comprehensive initial and ongoing training, unmatched by other CROs. Through our PACE Training Program, you will join other Professionals Achieving CRA Excellence:
- PACE provides the platform to effectively and confidently carry out your duties, enhance your current abilities and ultimately help you become a high-functioning independent Medpace CRA.
- PACE will prepare you by developing your CRA skills through interactive discussions and hands on job-related exercises and practicums.
- To supplement your in-house and field-based training you may also participate in other clinical research departmental core rotations, learning other aspects of the drug/device development and approval process.
Qualifications
- Minimum of Bachelor\’s degree in life science related field; advanced degree preferred;
- Previous experience as a CRC or equivalent, 1 year minimum;
- Willing to travel approximately 60-80% nationally;
- Familiarity with Microsoft Office;
- Strong communication and presentation skills;
- Steady job tenure;
- Full, permanent right to work in the UK;
- Already residing the UK;
- Must hold a valid drivers licence.
Medpace Overview
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries.
Why Medpace?
When you join Medpace, you become part of a team dedicated to supporting the development of ground-breaking drugs and devices. Our employees provide hope for those living with debilitating diseases. We invite you to be a part of something that is impacting millions of people around the globe while enjoying a competitive total compensation and benefits package and internal growth opportunities.
Awards:
- Medpace historically named a Top Cincinnati Workplace by the Cincinnati Enquirer
- Recognized by Forbes as one of America\’s Best Mid-size Companies in 2021
- Medpace ranks amongst top CROs for site ratings across all 10 important attributes including CRA training, preparation & organization, accessibility of staff, open communication, and ensuring timely drug availability
- Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
- Ranked in the top 10 on the 2021 LinkedIn Top Companies list in Cincinnati
What to Expect Next:
A member of our recruitment team will review your qualifications and, if interested, you will be contacted for an interview.
EO/AA Employer M/F/Disability/Vets #J-18808-Ljbffr
Entry CRA Virtual Networking Event for CRC\'s - UK employer: Medpace, Inc.
Contact Detail:
Medpace, Inc. Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Entry CRA Virtual Networking Event for CRC\'s - UK
✨Tip Number 1
Make sure to research Medpace thoroughly before the networking event. Familiarise yourself with their mission, values, and recent projects. This will help you engage in meaningful conversations with CRA Managers and demonstrate your genuine interest in the company.
✨Tip Number 2
Prepare thoughtful questions to ask during the event. Inquire about the PACE Training Program or the specific responsibilities of a CRA at Medpace. This shows that you're proactive and eager to learn more about the role and the company.
✨Tip Number 3
Network with other attendees as well. Building connections with fellow Clinical Research Coordinators can provide valuable insights and may lead to future opportunities. Don't hesitate to exchange contact information for follow-up discussions.
✨Tip Number 4
Follow up after the event with a thank-you email to the CRA Managers you spoke with. Express your appreciation for their time and reiterate your interest in the CRA position. This small gesture can leave a lasting impression and keep you on their radar.
We think you need these skills to ace Entry CRA Virtual Networking Event for CRC\'s - UK
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your experience as a Clinical Research Coordinator or equivalent. Emphasise relevant skills and achievements that align with the responsibilities of a Clinical Research Associate.
Craft a Compelling Cover Letter: Write a cover letter that expresses your enthusiasm for the role and the company. Mention why you are interested in Medpace and how your background in life sciences makes you a suitable candidate for the CRA position.
Highlight Relevant Experience: In your application, clearly outline your previous experience in clinical research, including any specific projects or responsibilities that demonstrate your capability to conduct monitoring visits and communicate effectively with site staff.
Prepare for the Networking Event: Since this is a networking event, prepare questions to ask the CRA Managers about their experiences at Medpace. This shows your interest and helps you make a positive impression during the event.
How to prepare for a job interview at Medpace, Inc.
✨Know Your Role
Make sure you understand the responsibilities of a Clinical Research Associate (CRA) at Medpace. Familiarise yourself with the key tasks such as conducting monitoring visits and ensuring compliance with protocols, as this will help you answer questions confidently.
✨Showcase Your Experience
Be prepared to discuss your previous experience as a Clinical Research Coordinator or equivalent. Highlight specific examples where you've successfully managed clinical trials or worked closely with medical site staff, as this will demonstrate your suitability for the role.
✨Prepare Questions
Think of insightful questions to ask the CRA Managers during the event. This shows your genuine interest in the position and helps you gather valuable information about the company culture and expectations.
✨Practice Communication Skills
Since strong communication is crucial for a CRA, practice articulating your thoughts clearly and concisely. Consider doing mock interviews with friends or family to build your confidence and improve your presentation skills.
