What are the responsibilities and job description for the LCRA/ CPM position at Upsilon Global?
LCRA/JR CPM
- $140000 - $170000 depending on experience
- Opportunity of growth
- Working on Oncology studies.
Upsilon Global are currently seeking an ambitious and driven LCRA/Jr CPM interested in joining a small but growing CRO in the New Jersey area. Our partner, an established CRO, are expanding their service offering and entering North America.
Currently working as a small team, they’ve got ambitious plans and are seeking an equally ambitious CPM to oversee the current portfolio as well as spearhead operations moving forward. The aim is to grow their presence and clinical portfolio as well as increase headcount, so this is a fantastic opportunity for anyone with ambitions of progressing to a Director of Clinical Operations role.
Main Responsibilities
- To oversee and lead American clinical operations Ensuring regulations, SOPs and GCP guidelines followed Managing budgets, deadlines, planning, resourcing and compliance Being the first point of contact for both internal and external meetings Maintaining the correct levels of resources Interviewing clinical personnel to expand the team when necessary Managing clinical and administrative personnel; this will include motivating, employing, training and assessing performances Reporting KPIs to management and implementing solutions to meet targets Assessing company policy and modifying solutions when necessary Contributing to the development of clinical SOPs and department guidelines to meet regulatory, ethical and clinical standards Setting agreed project targets and overseeing the quality of deliverables from the Clinical Operations teams Supporting daily duties including: responding to inquiries from clinical sites, project members and client requests, project management, site monitoring and general clinical activities associated with a small team Representing the Clinical Operations Department for proposals, budgets, P&L topics and contracts for the American and European markets
Education and Qualifications
- Lifesciences related degree (BSc/MSc/PhD) Previous experience as a clinical research associate Sound knowledge of ICH/GCP and regulatory requirements Experience using clinical trial management systems
Other skills and abilities
- In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines Ability to lead the clinical team, acting as advocate for the group Strong communication and interpersonal skills, including good command of English language Good presentation skills Ability to establish and maintain effective working relationships with co-workers, staff and clients
For further information on this opportunity and to learn of similar positions, please contact Upsilon Global at Rory.Pitts@upsilonglobal.com
LCRA/JR CPM
- $140000 - $170000 depending on experience
- Opportunity of growth
- Working on Oncology studies.
Upsilon Global are currently seeking an ambitious and driven LCRA/Jr CPM interested in joining a small but growing CRO in the New Jersey area. Our partner, an established CRO, are expanding their service offering and entering North America.
Currently working as a small team, they’ve got ambitious plans and are seeking an equally ambitious CPM to oversee the current portfolio as well as spearhead operations moving forward. The aim is to grow their presence and clinical portfolio as well as increase headcount, so this is a fantastic opportunity for anyone with ambitions of progressing to a Director of Clinical Operations role.
Main Responsibilities
- To oversee and lead American clinical operations Ensuring regulations, SOPs and GCP guidelines followed Managing budgets, deadlines, planning, resourcing and compliance Being the first point of contact for both internal and external meetings Maintaining the correct levels of resources Interviewing clinical personnel to expand the team when necessary Managing clinical and administrative personnel; this will include motivating, employing, training and assessing performances Reporting KPIs to management and implementing solutions to meet targets Assessing company policy and modifying solutions when necessary Contributing to the development of clinical SOPs and department guidelines to meet regulatory, ethical and clinical standards Setting agreed project targets and overseeing the quality of deliverables from the Clinical Operations teams Supporting daily duties including: responding to inquiries from clinical sites, project members and client requests, project management, site monitoring and general clinical activities associated with a small team Representing the Clinical Operations Department for proposals, budgets, P&L topics and contracts for the American and European markets
Education and Qualifications
- Lifesciences related degree (BSc/MSc/PhD) Previous experience as a clinical research associate Sound knowledge of ICH/GCP and regulatory requirements Experience using clinical trial management systems
Other skills and abilities
- In depth knowledge of, and skill in applying, applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines Ability to lead the clinical team, acting as advocate for the group Strong communication and interpersonal skills, including good command of English language Good presentation skills Ability to establish and maintain effective working relationships with co-workers, staff and clients
For further information on this opportunity and to learn of similar positions, please contact Upsilon Global at Rory.Pitts@upsilonglobal.com