Project Manager – Medical Communications – Surrey – Competitive Salary

Opening for an experienced Project Manager to join a well-known Medical Education agency. They are looking for talented Project Executives to work in close conjunction with the client company's Medical Education events lead, reporting directly to the Project Director.

The main purpose of the role is to manage projects which are high quality, on budget and meet deadlines while achieving a successful, ongoing client relationship on your projects.

Key responsibilities:

·        General project management, editing, writing and all types of project work (eg website development, other digital project work, research, mapping, use of design software, print management) to deliver work that is of a high standard, on time and within budget

·        Communicate professionally, swiftly and proactively with the client, making appropriate use of email and telephone contact

·        Communicate with KOLs/HCPs professionally, swiftly, politely and confidently, making appropriate use of email and telephone contact, providing them with all necessary information, eg what is expected from them and when by

·        Financial responsibility to ensure cost-efficiency

Competencies:

• Very high standard of written and spoken English
• Highly organised
• Fast, accurate editing – ability to spot mistakes
• Good writing skills – able to write a meeting report from attending an advisory board meeting
• Understand and write middle-weight medical information
• Good under pressure
• Teamwork and cooperation
• Rapport building

Skills, knowledge and experience:

• Scientific understanding – whether academic or through other work experience
• One year or more of experience of project management, account management, writing or editing within a medical communications agency or very similar work setting
• Writing/editing experience
• Efficient working knowledge of Microsoft Word and PowerPoint
• Manage teams to achieve goals – coordinating with others and coordinating the work of others

Fantastic opportunity for an experienced project manager to join a well-established Medical Education agency offering a competitive salary plus benefits!

 To discuss this role in more detail in confidence please call Rebekah Hill 0788029175

E-mail - rebekah@peoplewithchemistry.com Contact via LinkedIn: http://uk.linkedin.com/in/meetrebekahhillollow me on Twitter: http://twitter.com/meet_rebekah

Project Manager/Senior Project Manager – Top 5 CRO – Czech Republic

Project Manager/Senior Project Manager (PM): An internationally recognised top 5 CRO is currently expanding its clinical research team across CEE (Poland, Romania, Czech Republic & Hungary) on all fronts including Project Managers/Senior Project Managers. This is a brilliant time to join an industry leader in the pharmaceutical industry as they are steadily increasing their already extensive global client base. Joining this top CRO is a great career move for any Project Manager.

COMPANY BACKGROUND

The client is one of the top five CROs in the pharmaceutical and healthcare industry. They have an impressive global presence with offices in 50 countries and on-going clinical studies in over 100 countries. You will be given the chance to cover a broad spectrum of therapeutic areas from Phase I studies through to Phase IV, with extensive support, training and development given to staff at all stages of their career.

ROLE RESPONSIBILITIES

·         General project oversight

·         Financial management

·         Project implementation, control and evaluation

·         Client management

SKILLS DESIRED

·         Strong communication skills

·         Previous project management experience – 1+ year

·         Experience at a top CRO or Pharma

·         Degree in a science related field

Commutable locations: Field based, CEE (Poland, Romania, Czech Republic & Hungary)

Salary: €40-70,000 Per annum

 Full job description and company details are available upon application, apply below. This position is being dealt with by Paul Crawford at meet, call on 0044 203 178 7488 or 0044 777 233 8996 or email directly at paulc@peoplewithchemistry.com to discuss in confidence.

Find out more about us at www.peoplewithchemistry.com

Associated keywords: Project Manager, PM, Clinical Research Project Manager, CRO, clinical research, project management, project leader, international CRO, Clinical Project Manager, field based, office based, CEE, Romania, Poland, Hungary, Czech Republic, Project Manager, CRO.

Project Manager/Senior Project Manager – Top 5 CRO – Poland, Romania, Czech Republic & Hungary

Project Manager/Senior Project Manager (PM): An internationally recognised top 5 CRO is currently expanding its clinical research team across CEE (Poland, Romania, Czech Republic & Hungary) on all fronts including Project Managers/Senior Project Managers. This is a brilliant time to join an industry leader in the pharmaceutical industry as they are steadily increasing their already extensive global client base. Joining this top CRO is a great career move for any Project Manager.

COMPANY BACKGROUND

The client is one of the top five CROs in the pharmaceutical and healthcare industry. They have an impressive global presence with offices in 50 countries and on-going clinical studies in over 100 countries. You will be given the chance to cover a broad spectrum of therapeutic areas from Phase I studies through to Phase IV, with extensive support, training and development given to staff at all stages of their career.

ROLE RESPONSIBILITIES

·         General project oversight

·         Financial management

·         Project implementation, control and evaluation

·         Client management

SKILLS DESIRED

·         Strong communication skills

·         Previous project management experience – 1+ year

·         Experience at a top CRO or Pharma

·         Degree in a science related field

Commutable locations: Field based, CEE (Poland, Romania, Czech Republic & Hungary)

Salary: €40-70,000 Per annum

 Full job description and company details are available upon application, apply below. This position is being dealt with by Paul Crawford at meet, call on 0044 203 178 7488 or 0044 777 233 8996 or email directly at paulc@peoplewithchemistry.com to discuss in confidence.

Associated keywords: Project Manager, PM, Clinical Research Project Manager, CRO, clinical research, project management, project leader, international CRO, Clinical Project Manager, field based, office based, CEE, Romania, Poland, Hungary, Czech Republic, Project Manager, CRO.

Project Manager/Senior Project Manager – Top 5 CRO – Romania.

Project Manager/Senior Project Manager (PM): An internationally recognised top 5 CRO is currently expanding its clinical research team across CEE (Poland, Romania, Czech Republic & Hungary) on all fronts including Project Managers/Senior Project Managers. This is a brilliant time to join an industry leader in the pharmaceutical industry as they are steadily increasing their already extensive global client base. Joining this top CRO is a great career move for any Project Manager.

COMPANY BACKGROUND

The client is one of the top five CROs in the pharmaceutical and healthcare industry. They have an impressive global presence with offices in 50 countries and on-going clinical studies in over 100 countries. You will be given the chance to cover a broad spectrum of therapeutic areas from Phase I studies through to Phase IV, with extensive support, training and development given to staff at all stages of their career.

ROLE RESPONSIBILITIES

·         General project oversight

·         Financial management

·         Project implementation, control and evaluation

·         Client management

SKILLS DESIRED

·         Strong communication skills

·         Previous project management experience – 1+ year

·         Experience at a top CRO or Pharma

·         Degree in a science related field

Commutable locations: Field based, CEE (Poland, Romania, Czech Republic & Hungary)

Salary: €40-70,000 Per annum

 Full job description and company details are available upon application, apply below. This position is being dealt with by Paul Crawford at meet, call on 0044 203 178 7488 or 0044 777 233 8996 or email directly at paulc@peoplewithchemistry.com to discuss in confidence.

Find out more about us at www.peoplewithchemistry.com

Associated keywords: Project Manager, PM, Clinical Research Project Manager, CRO, clinical research, project management, project leader, international CRO, Clinical Project Manager, field based, office based, CEE, Romania, Poland, Hungary, Czech Republic, Project Manager, CRO.

 Pharmaceutical based in Switzerland has an urgent requirement for a Quality Assurance contractor.

1. Guide development teams in quality and compliance decision making to drive sustainable quality and compliance excellence 2. Provide leadership and guidance during the development and execution of corrective and preventive actions (CAPA) 3. Coordinate and review CAPAs to audits to ensure adequate root cause anal- ysis and systemic solutions 4. Lead formal investigations of issues as they arise, ensuring timely escalation to line management if critical observations are not resolved in due course 5. Identify ways to continuously improve quality and compliance with regula- tions and company standards, policies and procedures through partnership with Franchise personnel, Development Line Functions and Development QA groups 6. Represent Franchise QA in interactions with internal and external contacts and Health Authorities, as appropriate  7. Ensure inspection readiness by preparing clinical teams for FDA/EU/key HA pre-approval and sponsor-monitor inspections; provide inspection manage- ment support and follow-up post inspection  8. Ensure that Franchise compliance commitments are fulfilled on time  9. Provide interpretation of GCP regulations and company standards , guide- lines, policies and procedures to Franchise personnel  10. Drive the implementation of the annual Franchise Quality Plan; identify rele- vant areas to be addressed in future Quality Plans 11. Closely cooperate with the Franchise Continuous Improvement/Op Excel- lence groups; participate and provide Quality and Compliance input for pro- cess improvement teams  12. Closely cooperate with the Development QA Quality Systems Excellence, Au- diting and Compliance Excellence groups to ensure consistency of quality and compliance activities and effective communication  

Key Performance Indicators (Indicate how performance for this job will be measured)  

1. Quality and compliance guidance is routinely provided to the Franchise Project Teams as defined 2. Regulatory Commitments and audit CAPA are closed on time  3. Key Quality Indicators are tracked and assessed to proactively identify areas of potential risks and opportunities for continuous improvement 4. Issues are adequately and timely escalated

Regulatory Affairs Associate/RA Associate: This is a great prospect for an experienced Regulatory Affairs Associate to join a mid-size CRO where there is plenty opportunity for career progression. Maintaining a good work/life balance is encouraged and they provide plenty of training and support for their Regulatory Affairs Associates. This CRO understands that happy and motivated employees are their strongest asset.

COMPANY BACKGROUND

The client is a privately owned mid-size CRO with an international presence. They cover a wide range of therapeutic areas in all phases so it is a great company to gain experience with. Working from their UK headquarters in the Thames Valley you will be joining a friendly team dedicated to providing brilliant levels of customer service to their clients.

ROLE RESPONSIBILITIES

As a Regulatory Affairs Associate your responsibilities will include:

·         Regulatory affairs and technical writing activities

·         RA and EC submissions

·         Mentoring more junior Reg Affairs Associates and staff

·         Assisting RA management with project timelines, budgets, etc

SKILLS DESIRED

·         Strong experience in Regulatory Affairs and clinical trials – 18+ months

·         Life Sciences degree

·         Good knowledge of global regulatory guidelines

·         Knowledge of EU clinical trials directive

Commutable locations: Thames Valley – Office based

Salary: £30k - £45k (Level dependant) + benefits

Full job description and company details are available upon application, apply below. This position is being dealt with by Yasmin Dyer at meet, call on + 44 203 178 7488 or email directly at yasmin@peoplewithchemistry.com to discuss in confidence.

Find out more about us at www.peoplewithchemistry.com

Associated keywords: Regulatory affairs associate, RA associate, Senior regulatory affairs associate, CRO, contract research organisation, permanent, Thames Valley, Slough, Reading, UK, clinical research, regulatory affairs