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Chris Dott

Principal

VP Clinical Development at Orchard Therapeutics

Redhill, United Kingdom

Chris Dott's Work Experience

CSD Consulting

Principal

April 2006 to Present

CSD Consulting

Principal

April 2006 to Present

Inamed Ltd

Senior Director Clinical Affairs International

October 2005 to March 2006

Chris Dott's Education

Queen Mary College

Royal Free Hospital

School of Medicine PhD Biochemistry

University of London

PhD Biochemistry

Chris Dott's Professional Skills Radar Chart

Based on our findings, Chris Dott is ...

Empathetic
Visionary
Persuasive

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Based on our findings, Chris Dott is ...

50% Left Brained
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Chris Dott's Estimated Salary Range

About Chris Dott's Current Company

CSD Consulting

Frequently Asked Questions about Chris Dott

What company does Chris Dott work for?

Chris Dott works for CSD Consulting


What is Chris Dott's role at CSD Consulting?

Chris Dott is Principal


What is Chris Dott's personal email address?

Chris Dott's personal email addresses are c****[email protected], c****[email protected], and c****[email protected]


What is Chris Dott's business email address?

Chris Dott's business email addresses are not available


What is Chris Dott's Phone Number?

Chris Dott's phone +44 ** **** *336


What industry does Chris Dott work in?

Chris Dott works in the Pharmaceuticals industry.


About Chris Dott

📖 Summary

Principal @ From April 2006 to Present (9 years 9 months) Principal @ Set up my Drug Development Consultancy First Contract secured in April 2006; Projects undertaken include:- Writing and implementing Development Plans for NCEs (Biologics and small molecules) eCTD writing and compiling Auditing activities Economic assessment documentation Medical device development Publication writing From April 2006 to Present (9 years 9 months) Senior Director Clinical Affairs International @ Purpose and major challenge of the job: Create the Clinical Affairs (International) Department Run Global Development Programmes as agreed with EVP Clin Reg for New Products New Indications for approved products Contribute to Global Development Programmes run from USA to ensure International exposure Run Phase 4 studies for EU, Middle East and Africa Run PMS studies for EU, Middle East and Africa Run Local Registration Studies for EU, Middle East and Africa Provide EU, Middle East and Africa Markets Clinical support From October 2005 to March 2006 (6 months) Project Director / Global Project Leader @ Purpose and major challenge of the job Responsibility was for the development activities of multiple products with the objective of achieving regulatory approval on a world-wide basis. Responsible for the #1 / 2 Product in Development (among others) Annual budget responsibility was ~20% of Development spend Liaison with the marketing affiliates in order to achieve product acceptability to their markets. Development activity achieved through managing the multidisciplinary Product Groups /teams in order to ensure that the agreed strategy was executed efficiently and to agreed timelines, Ipsen SOP's and budget. The overall purpose of the job was to ensure that the strategy and execution of drug development within Ipsen was carried out in an efficient and high quality manner. From August 1999 to September 2005 (6 years 2 months) Director @ Purpose and major challenge of the job Direct Department of 14 professional clinical, regulatory and pharmacovigilance personnel in UK and USA to develop the products of the former Speywood Group for Ipsen Ltd. Review and sign off promotional material for the UK Market Responsible for the development strategy and its implementation Responsible for the development budget. Member of the Speywood Pharmaceuticals (Ipsen UK) Management Team From January 1998 to August 1999 (1 year 8 months) Director, Clinical Research @ Purpose and major challenge of the job Direct Department of 14 professional clinical regulatory and pharmacovigilance personnel in UK and USA to develop the products of the former Speywood Group for Ipsen. Review and sign off promotional material for the UK Market Responsible for the development strategy and its implementation Responsible for the development budget. From July 1997 to January 1998 (7 months) Clinical Research Manager @ Purpose and major challenge of the job Project manage the company's cardiovascular and neurotoxin drugs world-wide Manage the clinical development programme for two of the company's major drugs in cardiovascular and neurological medicine in Europe Prepare clinical data for regulatory submission including the Clinical Expert Reports Provide market support in terms of clinical studies, publications and symposia at International Meetings Review promotional material Manage 3 direct reports (Senior Clinical Research Scientists From April 1993 to July 1997 (4 years 4 months) Clinical Research Manager @ From October 1988 to April 1993 (4 years 7 months) Trial Manager @ Purpose and major challenge of the job To design, set up, co-ordinate, monitor and write reports on Phase I-Ill clinical studies conducted in UK, Europe, Africa, Australia and S Korea in order to support new drug applications to regulatory authorities Co-ordinate study team activities and agree work priorities for direct reports (CRAs From June 1985 to October 1988 (3 years 5 months) Senior Clinical Research Associate @ Purpose and major challenge of the job Manage the European (including Canada) development of granisetron (iv and oral) in chemotherapy and radiotherapy induced nausea and vomiting Write efficacy summaries for regulatory submission in Europe & USA Manage publication strategy for granisetron and provide clinical input into company sponsored symposia at International Meetings (Europe & USA) Write the protocols, design CRFs and write reports for pivotal studies Manage three CRA Develop world-wide (including USA) development plans (e.g. post operative nausea and vomiting) Responsible for European development of a drug for benign prostate hypertrophy From June 1985 to January 1988 (2 years 8 months) Research Technician @ Purpose and major challenge of the job Measurement of acute phase proteins in body fluids from patients with arthritic conditions Training of medical personnel in the techniques used in the research laboratory including protein purification and protein assays During this period of employment, I conducted my PhD research entitled; "The characterisation of alpha 2 macroglobulin in patients with rheumatoid arthritis". The degree was awarded in December 1984 Areas of clinical research covered in the pharmaceutical industry: From February 1978 to May 1985 (7 years 4 months) Queen Mary CollegeSchool of Medicine PhD, Biochemistry @ Royal Free HospitalPhD, Biochemistry @ University of LondonB.Sc. (2.2 Hons), Biology @ University of LondonUniversity of London Chris Dott is skilled in: Pharmaceuticals, Clinical Research, Clinical Trials, FDA, GCP, Biotechnology, Clinical Development, Program Management, Pharmaceutical Industry, Sop, Regulatory Submissions, Medical Devices, Drug Development, Neurology, Protocol, CRO


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In a nutshell

Chris Dott's Personality Type

Extraversion (E), Intuition (N), Feeling (F), Judging (J)

Average Tenure

4 year(s), 7 month(s)

Chris Dott's Willingness to Change Jobs

Unlikely

Likely

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