Spanish
Our client is a global healthcare leader based in Cork, Ireland. Their
goal is to make a difference for people around the world by
discovering, developing and delivering medicines that help people live
longer, healthier and more active lives. Central to all that they do
are their talented and motivated professionals, circa **Apply on the
website** of whom are based at their Global Business Solutions centre
in Little Island, Cork.
There they boast vibrant workforce made up of over **Apply on the
website** nationalities.
The Trial Capabilities Team provides clinical trial capabilities in
support of clinical development. The Clinical Trial Start Up Associate
is accountable to ensure the investigator sites meet requirements to
enrol study participants into clinical trials and support ongoing
activities during site maintenance and closeout.
RESPONSIBILITIES:
1. Contract Negotiations: ?
* communicating and negotiating contracts with the appropriate site,
team, or affiliate personnel (communicate on various contract issues,
identify relationship-building opportunities, secure site contracts,
collect site feedback, and facilitate communication with various
personnel, communicate and negotiate more complex contracts) ?1. TC
Process Improvement and Training: ?
* maintaining and conducting contract-related training (develop and
implement training for new contract associates and customers, create,
maintain, and distribute contract templates, process documentation,
and contract-specific documentation (such as the Legal Guidance
Document) as the contract process owner, act as a mentor to the
Contract Associates to provide the necessary guidance and knowledge
transfer to allow the contract associates to be successful
negotiators) ?
* providing clinical trial contract guidance to other business
partners (develop process documentation, facilitate quality, speed and
value through information sharing, , business partnership, and
assurance that all guidance is aligned with company`s policies,
clinical processes, and appropriate guidance, serve as the primary
contact and process owner for interactions between TC and the Legal
personnel related to process changes, documentation requirements, and
site contracting issues) ?1.
Contract Process Improvements: ?
* identifying and implementing improvements to the contracting
processes (standardizing and streamlining contract activities, as well
as using metrics to drive improvement throughout the entire
contracting process, increase contracting efficiency and effectiveness
by ensuring that learning is shared and leveraged, anticipate changes
by evaluating issues and opportunities, both internal and external,
and making recommendations to TC management)
REQUIREMENTS:
* Bachelor?s degree in a relevant discipline ?
* **Apply on the website** years of experience negotiating contracts
in clinical trials or similar ?
* Native Spanish speaker and fluency in English ?
* Strong organizational/time management skills, analytical skills,
negotiation skills, critical thinking skills
Other Information/Additional Preferences: ?
* Advanced degree or legal degree ?
* Thorough understanding of GDPR and other privacy regulations ?
* Experience negotiating privacy clauses with clinical research sites
?
* Experience working with global business partners and a global team Position: ?Clinical Trials Associate (Budgets & Contracts) fluent
Spanish
Our client is a global healthcare leader based in Cork, Ireland. Their
goal is to make a difference for people around the world by
discovering, developing and delivering medicines that help people live
longer, healthier and more active lives. Central to all that they do
are their talented and motivated professionals, circa **Apply on the
website** of whom are based at their Global Business Solutions centre
in Little Island, Cork.
There they boast vibrant workforce made up of over **Apply on the
website** nationalities.
The Trial Capabilities Team provides clinical trial capabilities in
support of clinical development. The Clinical Trial Start Up Associate
is accountable to ensure the investigator sites meet requirements to
enrol study participants into clinical trials and support ongoing
activities during site maintenance and closeout.
RESPONSIBILITIES:
1. Contract Negotiations: ?
* communicating and negotiating contracts with the appropriate site,
team, or affiliate personnel (communicate on various contract issues,
identify relationship-building opportunities, secure site contracts,
collect site feedback, and facilitate communication with various
personnel, communicate and negotiate more complex contracts) ?1. TC
Process Improvement and Training: ?
* maintaining and conducting contract-related training (develop and
implement training for new contract associates and customers, create,
maintain, and distribute contract templates, process documentation,
and contract-specific documentation (such as the Legal Guidance
Document) as the contract process owner, act as a mentor to the
Contract Associates to provide the necessary guidance and knowledge
transfer to allow the contract associates to be successful
negotiators) ?
* providing clinical trial contract guidance to other business
partners (develop process documentation, facilitate quality, speed and
value through information sharing, , business partnership, and
assurance that all guidance is aligned with company`s policies,
clinical processes, and appropriate guidance, serve as the primary
contact and process owner for interactions between TC and the Legal
personnel related to process changes, documentation requirements, and
site contracting issues) ?1.
Contract Process Improvements: ?
* identifying and implementing improvements to the contracting
processes (standardizing and streamlining contract activities, as well
as using metrics to drive improvement throughout the entire
contracting process, increase contracting efficiency and effectiveness
by ensuring that learning is shared and leveraged, anticipate changes
by evaluating issues and opportunities, both internal and external,
and making recommendations to TC management)
REQUIREMENTS:
* Bachelor?s degree in a relevant discipline ?
* **Apply on the website** years of experience negotiating contracts
in clinical trials or similar ?
* Native Spanish speaker and fluency in English ?
* Strong organizational/time management skills, analytical skills,
negotiation skills, critical thinking skills
Other Information/Additional Preferences: ?
* Advanced degree or legal degree ?
* Thorough understanding of GDPR and other privacy regulations ?
* Experience negotiating privacy clauses with clinical research sites
?
* Experience working with global business partners and a global team
We need : English (Good)
Type: Permanent
Payment:
Category: Others
