Clinical Protocol Associate
This vacancy has now expired. Please see similar roles below...
A leading scientific organization, known for its work in biomarker-driven cancer research, is seeking to recruit a Clinical Protocol Associate. The company, audits patients who have or are at risk of developing cancer, focuses on group research across Cancer Control and Outcomes, Therapeutic Studies, and Biomarker Sciences. Based in Massachusetts, this role is an exciting opportunity to provide expertise in the clinical field.
Job Responsibilities:
- Assisting with all aspects of coordinating protocol documents for clinical trials and correlative science studies to be conducted by the Group.
- Reviewing, editing, and formatting the protocol documents (and amendment documents for approved protocols) for scientific and editorial accuracy and consistency.
- Coordinating the work of a multidisciplinary team (physicians, statisticians, data managers, nurses, etc.) to facilitate the development of a clinical trial.
- Coordinating the Group-wide notification of any changes in the status of trials/studies; this includes activations, suspensions, and terminations.
- Maintaining computer database records related to protocol development and trial/study status changes.
- Regularly conducts quality control reviews for scientific and editorial accuracy as well as consistency with protocol documents.
Skills and Requirements:
- Bachelor's degree or equivalent work and/or life experience.
- Medical or biological sciences background is helpful but not required.
- Ideal candidates for this position will have editing or research experience and strong computer skills.
- Demonstrable multitasking, project management, and execution skills.
- Good interpersonal skills, including communication, presentation, persuasion, and influence.
- Good organisational skills, including efficiency, punctuality, and collaboration in a team environment.
- Proficiency with computer skills, such as MS Office.
To Apply:
Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please contact Mary Jacobs at +267-477-4800 or upload your CV on our website - www.Proclinical.com.
A full job description is available on request.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
#LI-MJ1
#ClinicalResearch
Related jobs
Highly Competitive
Frankfurt am Main (60488), Germany
Proclinical are seeing a Clinical Application Specialist for a position based in Frankfurt.
£45000 - £55000 per annum
City of London, England
Proclinical are searching for a dedicated professional for a Senior Clinical QA Specialist (GCP).
Up to £0.00 per annum
Zürich, Schweiz
Proclinical are currently supporting is a global management and technology consulting group as they are looking to recruit a Senior SAP FI/CO Consultant in Zurich, Switzerland.
Highly Competitive
Crailsheim (74564), Germany
Proclinical are seeking a dedicated Technical Project Manager to lead software development projects in the medical technology field.
Highly Competitive
Zürich, Schweiz
Proclinical are recruiting for a Senior Software Developer Java to join a consultant. This role is on a permanent basis and located in Zurich.
Highly Competitive
City of London, England
Proclinical are searching for a Clinical Project Manager for a fully remote role within the UK.
Up to US$27 per hour + Highly Competitive Salary
Philadelphia, USA
Proclinical Staffing is seeking a Cell Manufacturing Associate to join a cutting-edge cell and gene therapy company.
Highly Competitive Salary
Rockville, USA
Proclinical is seeking a dedicated and innovative QC Microbiologist with a focus on endotoxin detection methods. This is a contract position located in Rockville, MD.
Highly Competitive Salary
Cambridge, USA
Proclinical is seeking a dedicated Talent Acquisitions Coordinator. This is a contract position located in Cambridge, MA.
Highly Competitive Salary
Wilmington, USA
Proclinical is seeking a dedicated Senior Quality Specialist to provide leadership and oversight on GMP operations related to clinical manufacturing.