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PAREXEL International Corporation Job Title
Site Relationship Partner

PAREXEL International Corporation

Job Description
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Jobs at Parexel
We know just how important it is to put people first. It's with that human touch that we've played a part in nearly all of the top 50 treatments on the market. And every day, we're focused on working with industry leaders to bring life-changing healthcare to patients across the globe. Whether you join our Clinical, Consulting, Biotech, Functional Service Provider (FSP), or other teams, we're doing it
With Heart
Site Relationship Partner
Apply Now
Job ID
India, Remote
When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
In Parexel FSP we are currently looking for a Site Relationship Partner based in Mumbai, India.
Position Purpose:
The Site Relationship Partner (SRP) is the main Client point of contact for investigative sites, responsible for building and retaining relationships from site activation through the lifecycle of studies
The SRP is the face of the Client and therefore accountable for ensuring that sites receive necessary support and engagement, issues are resolved, and the Client’s reputation is that of Partner of Choice.
The SRP proactively collaborates and provides local intelligence to country outreach surveys, targeted sites strategies, study design, and Client pipeline opportunities
Primary Duties:
Responsible for relationship building and management
Usher investigator sites through site activation and study activities from study start up to close out.
Maintain regular communications with investigator sites to gather status updates, informal and formal performance metrics, and study-level feedback
Act as the main point of contact for all site- and study-level questions, liaising with and escalating to appropriate teams to respond and resolve questions. Follow up and close issue status with investigators to ensure awareness of resolution
Responsible for proactively providing local intelligence
Provide country/regional level input to country outreach surveys including protocol feasibility, country Standard of Care (SOC) and medical practices
Provide country/regional level input to country strategy/planning and site recommendation through intimate understanding of country, sites, processes and practices, and associated site performance metrics
Accountable for study start-up, activation, and execution to plan
For targeted sites
Deploy Global Site and Study Operations (GSSO) targeted site strategy by qualifying and activating targeted sites, while coordinating Client functions to standardize processes and deliver activation in line with the targeted site strategy
Confirm (and educate where needed) that sites are familiar with Client requirements for study start up and facilitate the availability of Master Service Agreements (MSAs) when feasible
For all sites
Provide enrollment support and ensure progress by responding to start up and recruitment issues from investigators, partner with study team to define and support recruitment initiatives at site / country level
Maintain a thorough knowledge of assigned protocols
The Individual:
A scientific or technical degree in the healthcare area is preferred along with extensive knowledge of clinical trial methodology
Skills in more than one language are an advantage in this role; English is required
Experience with drug development and monitoring (preferred)
Experience implementing centrally designed and developed initiatives on a local basis
Demonstrated knowledge of quality and regulatory requirements for applicable countries
Demonstrated knowledge of site intelligence at country/cluster level in support of site recommendation
Demonstrated knowledge of clinical trial methodology and the drug development process, related to monitoring clinical trials, Good Clinical Practice (GCP), Food and Drug Administration (FDA), or country-specific regulatory environment
Availability to travel regularly within country and region is required
Effective verbal and written communication skills in relating to colleagues and associates both inside and outside of the organization
Apply Now

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