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Job type: Permanent

Discipline: Project/Study Manager (CSM/CPM), Program Manager / Director, Clinical Scientist

Location: United States

Proclinical is currently recruiting for a Clinical Trial Manager with a pharmaceutical company located in Philadelphia, PA.

Job Responsibilities:

Primary clinical point of contact with the client
Collaborate with PM on monthly invoicing and variance management of clinical budget
Develop study related clinical documents (e.g. clinical plans, Informed Consent Form templates, study specific forms and manuals, CRF completion guidelines, study trackers, PSV/SIV slides and other training materials)
Identify and develop training needs for CRAs and third-party vendors specific to the study, protocol and practices including presenting these at Investigator Meetings and Study Kick-off meetings
Lead internal clinical team meetings and sets expectations for clinical team of CRAs and CTAs
Address all CRA and site questions and maintains Frequently Asked Question (FAQ) log as appropriate
Support in planning and conducting investigator meetings
Develop clinical monitoring strategies for assuring study timelines are met and assuring quality deliverables
Responsible for eTMF implementation and management
Work closely with PM for project-specific resourcing issues
Collaborate with data management and CRAs to ensure data quality and compliance with data cleaning timelines

Skills and Requirements:

Bachelor's degree or equivalent combination of education/experience in science or health-related field.
Advanced degree preferred
Minimum of 5 years of clinical research experience

If you are having difficulty in applying or if you have any questions, please contact Bri Copeland at 267-297-3280.

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.

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