Patient Report Outcomes/Clinical Outcomes Assessment Scientist
- Employer
- Proclinical Staffing
- Location
- USA, Cambridge, Massachusetts
- Salary
- Negotiable
- Start date
- 1 Oct 2024
- Closing date
- 15 Oct 2024
View moreView less
- Discipline
- HEOR, Market Access
- Hours
- Full Time
- Contract Type
- Contract
- Experience Level
- Experienced (non-manager)
Job Details
Patient Report Outcomes/Clinical Outcomes Assessment Scientist - Contract - Remote
Proclinical is seeking a Patient Report Outcomes/Clinical Outcomes Assessment Scientist for a fully remote, 12+ month W-2 contract.
Primary Responsibilities:
The successful candidate will be part of the Patient Centered Outcomes (PCO) team, which is crucial in developing integrated evidence plans to support patient-centric drug development. Your work will ensure that strong PRO/COA strategies are in place to demonstrate the value of our products to patients, physicians, payers, and regulators.
Skills & Requirements:
- Bachelor's degree required; Master's degree preferred.
- Relevant experience in the development and implementation of PRO/COA strategies.
- Strong background in pharmaceutical, regulatory, or academic settings.
- Excellent cross-functional collaboration skills.
- Ability to communicate complex scientific concepts clearly.
- Experience in developing and validating PRO/COA instruments.
- Knowledge of regulatory guidelines and methodologies.
The Patient Report Outcomes/Clinical Outcomes Assessment Scientist's responsibilities will be:
- Define and oversee the execution of strategies for the rigorous development and implementation of PRO/COAs across the portfolio.
- Guide the development, validation, analysis, interpretation, and utilization of PRO/COA instruments in clinical trials and/or observational studies.
- Collaborate with cross-functional teams (e.g., clinical operations, biostatistics) to ensure clear communication and appropriate implementation of patient-centric endpoints in clinical trials.
- Support regulatory communications by developing targeted questions and identifying critical evidence for meetings to support patient-centric endpoint strategies.
- Contribute to the broader publication strategy by planning and contributing to external publications, including scientific abstracts and peer-reviewed manuscripts.
- Stay informed about scientific and regulatory changes across specialty and primary care drug development programs.
- Pursue ongoing learning to understand and adopt evolving methodologies and guidelines, and communicate findings to cross-functional groups as needed.
If you are having difficulty in applying or if you have any questions, please contact Bodin Forsen at B.Forsen@proclinical.com.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
Company
At ProClinical we have one aim: to support life science companies in the many challenges they face while combatting unmet medical need worldwide.
Ageing populations, rare diseases, epidemics and the millions of patients without access to medication are just a few of the pressing issues that life science companies contend with. The industry is under increasing pressure to develop new and innovative ways to save and improve patients’ lives.
ProClinical’s mission is to support their work by connecting life science companies with the highly skilled professionals they need to continue innovating.
Internal recruitment and HR teams often struggle to continuously source skilled, experienced professionals to fill highly-specialised and niche roles. ProClinical combines a deep understanding of the industry with extensive candidate networks to provide both a technical and cultural fit for our life science partners.
- Website
- https://www.proclinical.com/
- Telephone
- 0800 988 4437
- Location
-
Eldon House
Eldon Street
London
EC2M 7LS
GB
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