Harriet Clayton is a Clinical Trial Support Team Coordinator at Rare Disease Research Partners (RDRP). In this role, she organises travel and accommodation for patients and their families and arranges for reimbursement of expenses in order to make participating in the clinical trial as stress-free as possible.
Before joining RDRP, Harriet studied for a BA in French and then worked as an administrator for a law firm whilst studying for a postgraduate certificate in translation.
Harriet enjoys helping people from all over the world participate in clinical trial research and feels grateful that she can ease some of the pressure for families who face enough challenges without the stress of making complicated travel arrangements.
Pauline Grant is a Clinical Trial Support Team Coordinator at Rare Disease Research Partners (RDRP). In this role, she provides worldwide logistical support and assistance to patients and their families to ensure that they are able to attend their study visits.
Before joining RDRP, Pauline spent 12 years working as Deputy Manager of a Montessori Nursery School. Pauline has a Certificate in Management and an AMI Diploma in Montessori Pedagogy.
Pauline feels very rewarded by her role within the Clinical Trial and Patient Access team, as she is able to play a part for each family on their journey to improve the life of the patient.
Lianne Mott is a Clinical Trial Support Team Coordinator at Rare Disease Research Partners (RDRP). In this role, Lianne is responsible for assisting patients and their families to participate in clinical trials. This involves sourcing suitable travel and accommodation options for study visits, reimbursing study related expenses and assisting with the relocation of families, often to another country, to enable them to take part in worldwide clinical trials.
Before joining RDRP, Lianne worked in the financial sector managing corporate events. She also gained multiple skills during her many years as airline cabin crew.
Lianne finds her role very rewarding and knows that she is able to take away some of the stress from patients and families when they are planning for a clinical trial study visit, allowing them to focus on the clinical trial itself.
Joanna Slade (Jo) is a Clinical Trial Support Team Coordinator at Rare Disease Research Partners (RDRP). In this role, Jo arranges travel and accommodation for patients attending clinical trials and the reimbursement of their travel expenses. Before joining RDRP, Jo spent 16 years working for the NHS, mainly in GP surgeries.
Jo has a BA in Hotel and Catering Management and a Post Graduate Diploma in Human Resource Management. Jo enjoys assisting patients and their families with all aspects of their travel and is keen to do all she can to make planning their time away from home less stressful, so they can concentrate purely on their participation in their clinical trial.
Contact us t. +44 (0) 345 260 1087 e. email@example.com
MPS House Repton Place, White Lion Road Amersham, Buckinghamshire, HP7 9LP
MPS Commercial is a Private Limited Company Registered No 08621283. MPS Commercial trades as Rare Disease Research Partners and is a wholly owned, not for profit subsidiary of the Society for Mucopolysaccharide Diseases (the MPS Society), Registered Charity in England and Wales No 1143472. Rare Disease Research Partners social objectives are to reinvest any surplus to support the mission of the MPS Society to transform the lives of patients through specialist knowledge, support, advocacy and research.