PRIMEVIGILANCE is looking for employees for positions:
sales account manager
Trade
sales
Sales
Language
english
Working hours
full-time
Responsibility
company Description
we are PrimeVigilance , a specialised mid-size pharmacovigilance service provider established in 2008
we cover all therapy areas including medical device
we love investing in our staff by providing an excellent training and development platform
generate and pre-qualify new leads by using appropriate company resources, programs and tools
research leads and identify relevant prospects through various systems and data pools
approach relevant prospects and generate interest via e-mail or phone call to create new business opportunities
primeVigilance provides first class support to our small to large pharmaceutical and biotechnology partners maintaining long lasting relationships and has become one of the global leaders in its field
Requirements
bachelors Degree or Equivalent
demonstrated experience working in an Inside Sales position in a CRO or other vendor within the clinical trials industry
experience in developing new business, lead nurturing and qualification, prospecting and appointment setting
good understanding of Phase I-IV clinical development
strong written and verbal communication skills to clearly and concisely present information on calls and via email
drive and determination to succeed as well as meet and exceed targets
must be adaptable, professional, and motivated
ability to listen and identify pain points and customer challenges
manager
Working hours
full-time
Language
english
Responsibility
we are looking to strengthen our growing Medical Information Management Team
supporting all aspects of outsourced Medical Information service delivery including, programme management, Medical Information services set-up, program expansion and program compliance
the role will be focused on supporting a Medical Information Team in the delivery of Medical Information Services
developing client relationships, identify and implement process improvements and supporting business development
the successful applicant will be responsible for client communication and service delivery for global MI programs
participates in client audits and inspections
line management of a Medical Information Team. Responsible for leading, educating and mentoring and enquiry handlers to provide the highest quality Medical Communications services
ensuring the delivery of a high quality MI service, and for maintaining compliance with KPIs, regulations and company policies in accordance with any Pharmacovigilance and Medical Information agreements
Requirements
life Science Degree or equivalent. Healthcare degree is an advantage
program management experience, preferably in a Pharmacovigilance or Medical Information environment
prior experience supervising within a Call Center operation, preferably in a Medical Information environment
experience mentoring, training and line management
critical thinking and creative problem solving skills
relationship building skills
excellent communication skills
additional Information
quality manager
Working hours
full-time
Language
english
Requirements
life Sciences degree
educated to degree standard or appropriate equivalent work experience
strong previous pharmacovigilance experience including quality and compliance experience within a GxP environment
previous experience in a Quality and/or Compliance-related role
good organisational skills, attention to detail and excellent communications skills
previous line management experience ·
must have leadership qualities
prior experience with electronic Document Management or Training Management systems
Responsibility
the Quality Manager is responsible for leading the Procedures team
they drive quality
this team ensures that PrimeVigilance’s controlled procedures and training activities are managed in compliance with global regulations, legislation and PrimeVigilance requirements
core responsibilities
the Quality Manager leads, educates, mentors and develops the Procedures team to ensure their competence and confidence in their assigned roles
oversight of all project related quality activities
ensures support to all PrimeVigilance functional teams in developing, managing and implementing PrimeVigilance Controlled Procedures and related training
drive project related quality improvement and providing quality advice
senior project manager
Working hours
full-time
Language
english
Requirements
PV Project Management experience from ideally a service provide / CRO
health Care Professional or Life Science Graduate
be comfortable with communicating at senior levels within pharmaceutical organizations
have good leadership qualities including skills in planning, mentoring, meeting facilitation, communication and problem solving
additional Information
proven track record of demonstrated Pharmacovigilance activities including processing and quality review of ICSRs, writing, or contributing to aggregate reports, literature screening, reconciliation, and preparation of SOPs
strong experience in either of the following: Medical Device, Vaccines, Gene Therapy or Biosimilars
Responsibility
experienced home-based project managers will also be considered where we have European entities
key Responsibilities
acting as the primary contact point for project-related matters
preparing project scope and objectives based on the signed agreement between the client and PrimeVigilance
primeVigilance is continuing to expand and is looking for an experienced Pharmacovigilance Project Manager/Senior PM to join our dynamic, rapidly expanding organisation
project activities planning, including deadlines and interim milestones
based in any of our offices, the PV Project Manager will be responsible for leading and managing long term engagements with our clients
reporting for the client and the PrimeVigilance management, e.g., preparation of Monthly reports, serving as basis for invoicing
team manager
Language
english
Responsibility
leads the team responsible for ICSR management for a selected project or group of projects as Team Leader
ensures adequate distribution of tasks for assigned projects and teams and oversees the workflow process
assures and exerts of activities leading to effective cooperation with clients in the area of ICSR Management
contributes to achieving company´s goals and objectives
works under supervision of ICSR Operational Lead
providing support to other activities undertaken by the project team on behalf of the client and the company
line Manages assigned ICSR staff
proposes process changes to ICSR Operational Lead
Requirements
life science graduate, pharmacy, nursing, other healthcare related qualification or experience in pharmacovigilance
strong previous experience of PV in ideally a CRO environment
previous experience in a Line Management position
excellent communication skills
organization skills, including attention to details and multitasking
delegation skills
planning and time management
technical skills
project manager
Trade
legal
Legal
Language
english
Requirements
PV Project Management experience from ideally a PV service provider/ CRO
health Care Professional or Life Science Graduate
be comfortable with communicating at senior levels within pharmaceutical organizations
have good leadership qualities including skills in planning, mentoring, meeting facilitation, communication and problem solving
proven track record of demonstrated Pharmacovigilance activities including processing and quality review of ICSRs, writing, or contributing to aggregate reports, literature screening, reconciliation, and preparation of SOPs
Responsibility
acting as the primary contact point for project-related matters
preparing project scope and objectives based on the signed agreement between the client and PrimeVigilance
project activities planning, including deadlines and interim milestones
reporting for the client and the PrimeVigilance management, e.g., preparation of Monthly reports, serving as basis for invoicing
managing client’s expectations to make sure the client is satisfied with services of PrimeVigilance, and that the work PrimeVigilance delivers meets, or even exceeds, the clients’ expectations
writer
Language
english
Requirements
previous experience of pharmacovigilance medical writing, including PBRERs, DSURs, RMPs writing
life Science degree, or have equivalent nursing or medical qualifications
ability to manage multiple and varied tasks and prioritize workload with attention to detail
ability to effectively train and mentor Associate Medical Writers
Responsibility
independent authoring, editing and reviewing of various regulatory/clinical documents (e.g
the PrimeVigilance Senior Medical Writer position offers a unique opportunity to further develop your career in the field of drug safety
support in all pharmacovigilance operations associated with medical writing
continuous self-education in all aspects associated with medical writing
managing a team of junior medical writers
aggregate reports, risk management plans and other documents needed throughout the product’s life cycle) with the responsibility for the quality and content of the document and compliance with internal and external standards
active participation in trainings and development, implementation and maintenance of quality system documents for medical writing, including internal templates and formats required for standardised documentation