Our client is urgently seeking several CTA's, CRA's & CTM's with obesity or oncology Therapeutic Area.
CTA:
The position requires 3-5 years of biotechnology/pharmaceutical/clinical trial management experience, with advanced degrees preferred.
Candidate should bring a global perspective, be able to work cross-functionally, and promote a collaborative and inclusive work environment.
Strong decision-making is essential, as the role demands quick, sound judgment based on input from multiple stakeholders.
Excellent communication, negotiation, and influencing skills are key for managing relationships across internal and external teams.
Overall, the candidate must be organized, confident, and capable of working both independently and within a team.
CRA:
Serves as a crucial member of the project team for the quality execution of assigned clinical protocols according to SOPs, ICH/GCP, and corporate and departmental program goals.
Supports the Study Lead as an integral member of a multifunctional team to ensure clinical study activities including study start-up, enrollment, maintenance, and closeout are executed appropriately.
Participates in protocol development, tracking changes for future protocol amendments, and works with medical writing to initiate protocol amendments as needed.
Oversees aspects of study management and vendors (e.g. IRT, eCOA, cardiac safety, patient reimbursement vendors) to ensure high quality of data and to ensure study execution and deliverables are met with minimum supervision.
Overall management of selected clinical sites including acting as a point of escalation and oversight of CRO monitoring activities, which includes monitoring visit report review, contract and budget negotiations with clinical sites.
CTM:
Leads and coordinates global cross-functional study teams through all study stages (start-up, conduct, close-out).
In collaboration with internal stakeholders, responsible for helping to drive the RFP and RFI process, analyze service providers, budgets and proposals, conduct bid defense meetings, award services, negotiate and execute complex agreements (i.e., CRO, study related collaboration agreements).
Provides oversight and direction to the CRO and service providers to accurately coordinate clinical study activities.
If you have the experience mentioned above, please send me your updated resume.
