What are the responsibilities and job description for the Innovative Medicine Scientific Affairs Consultant position at ClinChoice?
Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it's the best of both worlds….
ClinChoice is searching for an Innovative Medicine Scientific Affairs Consultant to join one of our clients.
ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client's counterparts.
Main Job Tasks and Responsibilities:
Innovative Medicine Scientific Affairs Consultant
US Commercial Pharmacovigilance Contractor
Position Description:
Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.
Who will you be working for?
About ClinChoice
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.
Our Company Ethos
Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates.
ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.
Key words: PV, Pharmacovigilance, Regulatory
ClinChoice is searching for an Innovative Medicine Scientific Affairs Consultant to join one of our clients.
ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client's counterparts.
Main Job Tasks and Responsibilities:
Innovative Medicine Scientific Affairs Consultant
US Commercial Pharmacovigilance Contractor
Position Description:
- Supplier is supporting US Operating Company Pharmacovigilance oversight to ensure that internal and external organizations are compliant with Pharmacovigilance regulatory requirements, as part of the conduct of non-interventional studies and patient support programs.
- SERVICES: Supplier will provide the following Services:
- Review open RRAs to create a listing of non-compliances
- Work with Buyer to establish processes for addressing different areas of non-compliance
- Review RRAMS data and remediate training for those RRA team members that have not completed AE/PQC training
- Review RRAMS data to identify contracts without PV exhibits and escalate to Buyer for remediation
- Routinely liaise with internal and external partners to complete required activities
- Support the close out of RRAs
- Attention to detail and accuracy in data review and reporting.
- Strong communication and collaboration skills for working with cross-functional teams.
- Ability to work in a fast-paced environment and manage multiple tasks with deadlines.
- Candidate has a BS degree with 2 – 3 years of experience.
- On-Site Titusville or Horsham office 2 -3 days a week.
Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.
Who will you be working for?
About ClinChoice
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.
Our Company Ethos
Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates.
ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.
Key words: PV, Pharmacovigilance, Regulatory
