At a Glance
- Tasks: Lead and manage clinical trial transparency projects while collaborating with clients and regulatory authorities.
- Company: Join MMS, an award-winning CRO known for its innovative culture and exceptional employee satisfaction.
- Benefits: Enjoy remote work flexibility, a supportive team environment, and opportunities for professional growth.
- Why this job: Shape the future of clinical research in a role that values your contributions and fosters collaboration.
- Qualifications: Graduate degree in a relevant field and 6+ years in clinical trial transparency or medical writing.
- Other info: Be part of a globally recognised team making a real impact in the pharmaceutical and biotech industries.
The predicted salary is between 43200 - 72000 £ per year.
This job is brought to you by Jobs/Redefined, the UK\’s leading over-50s age inclusive jobs board. Are you looking to join a company where your contributions truly matter, and where you\’ll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research. Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit www.mmsholdings.com or follow MMS on LinkedIn. Responsibilities: Interact with clients and regulatory authorities, remotely and onsite, including representation at key regulatory meetings on behalf of the client. Demonstrated ability to lead/ manage multiple individuals and/or groups. Cross-functionally collaborates and coordinates Transparency deliverables ensuring that timelines and milestones remain on-track and within target. Strategically assesses resource utilization and forecasting to ensure companywide goals are met Effectively communicates complex strategic concepts with ability to tailor message to targeted audience. Demonstrate thought leadership with customers by developing and presenting client industry trends, benchmarking, and other pertinent information. May participate in industry events for this purpose. Demonstrated ability to lead / manage multiple individuals and/or groups in a global environment. Directs strategic planning and proactively prepares contingency plans to address unforeseen challenges within group, and cross functionally to ensure uninterrupted delivery and maintain compliance. Ability to facilitate positive group morale and productivity by appropriately including others in decisions/plans. Manages staff, makes decisions and advises others on complex problems; understands intra- and inter-departmental implications of decisions and can develop strategic solutions with minimal input. Direct, manage, and oversee the daily activities and workload of the transparency, PLS, and redaction teams. Proactively identifies areas for improvement before issues arise and provides strategic proposal/resolution for consideration. Develops and leads teams with diverse experience and skill sets to achieve intra and inter departmental goals. Requirements: Graduate degree in scientific, medical, clinical discipline or related field, or related experience, Masters preferred. Minimum of 6 years\’ experience in clinical trial transparency, disclosure, or medical writing role At least 5 years of experience in a CRO environment. Demonstrated managerial skills and experience preferred. High level knowledge of drug development process, clinical development, and operations, with a strong understanding of regulatory guidelines. Excellent scientific writing skills. Excellent analytical, organizational, and problem-solving skills. Proficiency with MS Office applications. Strong communication and presentation skills. Knowledge of ISO 9001, ISO 27001, 21 CFR Part 11, FDA, and GCP requirements Understanding of CROs and scientific & clinical data/ terminology, & the drug development process. #J-18808-Ljbffr
Contact Detail:
MMS Holdings Inc. Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Manager, Clinical Trial Transparency & Disclosure (Remote)
✨Tip Number 1
Familiarise yourself with the latest trends and regulations in clinical trial transparency and disclosure. This knowledge will not only help you during interviews but also demonstrate your commitment to staying updated in this rapidly evolving field.
✨Tip Number 2
Network with professionals in the clinical research industry, especially those who work in CROs. Engaging with them on platforms like LinkedIn can provide insights into the company culture at MMS and may even lead to referrals.
✨Tip Number 3
Prepare to discuss your experience in managing teams and projects, particularly in a remote setting. Highlight specific examples where you successfully led cross-functional collaborations or navigated complex regulatory challenges.
✨Tip Number 4
Showcase your thought leadership by being ready to discuss industry benchmarks and trends. Consider preparing a brief presentation or talking points that illustrate your understanding of the current landscape in clinical trials.
We think you need these skills to ace Senior Manager, Clinical Trial Transparency & Disclosure (Remote)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical trial transparency and disclosure. Emphasise your managerial skills and any specific achievements in a CRO environment that align with the job requirements.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and your understanding of the drug development process. Mention how your background and skills make you a perfect fit for the Senior Manager role at MMS.
Highlight Relevant Experience: In your application, clearly outline your experience in managing teams and projects within a clinical research setting. Use specific examples to demonstrate your ability to lead and communicate effectively with clients and regulatory authorities.
Showcase Your Analytical Skills: Since the role requires strong analytical and problem-solving skills, include examples of how you've successfully navigated complex challenges in previous roles. This will help illustrate your capability to proactively identify areas for improvement.
How to prepare for a job interview at MMS Holdings Inc.
✨Research the Company
Before your interview, take some time to learn about MMS and its role in the clinical research industry. Understand their values, culture, and recent achievements. This will help you tailor your responses and show genuine interest in the company.
✨Prepare for Scenario-Based Questions
Given the managerial nature of the role, be ready to discuss specific scenarios where you've successfully led teams or managed complex projects. Use the STAR method (Situation, Task, Action, Result) to structure your answers effectively.
✨Showcase Your Communication Skills
As the role involves interacting with clients and regulatory authorities, demonstrate your strong communication skills during the interview. Practice explaining complex concepts clearly and concisely, as this will be crucial in your potential role.
✨Highlight Your Problem-Solving Abilities
Be prepared to discuss how you've identified and resolved issues in previous roles. Share examples that showcase your analytical and organisational skills, particularly in a CRO environment, to illustrate your fit for the position.