Associate Manager, Clinical Operations Site Management - Italy/Spain/Serbia- Remote (Roma)

Associate Manager, Clinical Operations Site Management - Italy/Spain/Serbia- Remote (Roma)

31 ago
|
Worldwide Clinical Trials
|
Roma

31 ago

Worldwide Clinical Trials

Roma

ph3Who We Are /h3 pWe’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. /p h3Who We Are /h3 pWe’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. /p pWe are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way. /p pOur mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit. /p h3Why Worldwide /h3 pWe believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands‑on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us! /p h3What Clinical Operations Site Management Does At Worldwide /h3 pEmbark on a fulfilling Clinical Operations career as you leave a lasting impact on patients’ lives. Join Worldwide Clinical Trials for an unparalleled CRO experience, where you can drive extraordinary scientific breakthroughs and contribute to the very heart of every successful clinical trial. /p pWorking alongside brilliant minds across a variety of therapeutic areas, you will have the chance to collaborate closely with top‑tier colleagues from diverse backgrounds and specialties. Our commitment to advancing clinical research is cultivated in a supportive,



team‑oriented atmosphere, with our hands‑on leadership and dedicated team members working together to innovate and solve complex challenges for our customers. /p h3What You Will Do /h3 ul liResponsible for interviewing and selecting CRA/IHCRA candidates and ensuring consistent onboarding of permanent and contract CRAs/IHCRAs /li liEnsure CRAs are properly and timely trained to perform all types of visits as well as other billable monitoring activities /li liProvide on‑site mentoring for CRAs through observation or site assessment visits /li liEstablish regular communication and1:1 calls with CRAs/IHCRAs to review and discuss quality metrics (SVR compliance, SDV metrics, TMF readiness, expense report submissions, project status, etc.) /li liAct as point of escalation for CRA/IHCRA performance issues on projects /li liReview Time Cards, including review and approval of hours billed by contractors /li liReview the accuracy of Sciforma assignments and workload /li liConduct performance appraisals, rewarding and disciplining employees, addressing employee relations issues and resolving problems /li liWrite and conduct CAPAs when necessary; Support Directors of Clinical Operations /li liApprove CRA/IHCRA PTO requests /li liReview and approve CRAs/IHCRAs' non-billable expenses /li /ul h3What You Will Bring To The Role /h3 ul liAbility to understand multiple study protocols. /li liSuperior oral and written communication skills. /li liStrong planning and organizational skills. /li liGood interpersonal skills. /li liExperienced problem solving/decision making skills. /li liGood attention to detail. /li liUnderstanding of clinical research principles and process, data collection and editing skills. /li liAbility to navigate in EDC software (InForm, Medidata, etc.)



/li liStrong knowledge of FDA regulations, ICH Guidelines and HIPAA. /li liUnderstanding of standard operating procedures. /li liKnowledge of therapeutic areas. /li liKnowledge of Word, Excel and Outlook /li /ul h3Your Background /h3 ul liFour-year college curriculum with a major concentration in biological, physical, health, pharmacy or other related science and six years clinical research experience as a clinical research associate OR /li liTwo-year college curriculum (unless nursing degree then see requirement above) or equivalent education/training and seven years clinical research experience as a clinical research associate OR /li liEight years of clinical research experience as a clinical research associate or other position directly related to clinical research with a pharmaceutical or biotechnology company /li liTravel required/Valid passport required /li /ul pWe love knowing that someone is going to have a better life because of the work we do. /p pTo view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit or connect with us on LinkedIn. /p pWorldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable lawb. /b /p /p #J-18808-Ljbffr

📌 Associate Manager, Clinical Operations Site Management - Italy/Spain/Serbia- Remote (Roma)
🏢 Worldwide Clinical Trials
📍 Roma

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