Regulatory Affairs Specialist - Montenegro -Contractor -Remote

Regulatory Affairs Specialist - Montenegro -Contractor -RemoteJoin to apply for the Regulatory Affairs Specialist - Montenegro -Contractor -Remote role at Worldwide Clinical TrialsContinue with Google Continue with GoogleRegulatory Affairs Specialist - Montenegro -Contractor -RemoteJoin to apply for the Regulatory Affairs Specialist - Montenegro -Contractor -Remote role at Worldwide Clinical TrialsWho We AreWe'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.Who We AreWe'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.We 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.Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.Why WorldwideWe 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!What The Regulatory Affairs Department Does At WorldwideRegulatory Affairs is pivotal in navigating the complex regulatory landscape, ensuring the success of diverse clinical trials.

As subject matter experts, the team leads submissions to regulatory authorities, coordinates with ethics committees across EMEA, Asia Pacific, and Latin America, and ensures compliance with evolving regulations.

Their expertise drives the development and approval of innovative medical products, supports business development efforts, and offers strategic guidance on contract negotiations.

They also mentor junior staff, review key documentation for global regulatory standards, and keep all stakeholders informed throughout the submission processWhat You Will DoYou will be a subject matter expert and local point of contact for activities supporting Regulatory submissions, site activation and maintenance for awarded projects.You will be responsible for planning, initiating, and tracking documents required for regulatory submissions, essential documents collection, review, and provision of country / site / EC requirements to support the achievement of site activation goals and communicating status, risks and actions related to any start-up activities and maintenance when applicable.What You Will Bring To The RoleStrong organizational and management skills.

Strong planning, strategizing, managing, monitoring, scheduling, and critiquing skills.Self-motivated learning about current regulatory processes and intelligenceProactive by identifying potential issues in the process and anticipating solutionsThorough understanding of country-level cultural norms and local healthcare systems; ability to initiate and develop relationships with local investigators and key site personnelEasily adjusts to a changing environment; ability to prioritize and adapt between detailed and strategic activities while maintaining delivery timelines and qualityTeam-oriented work style; seeks and gives guidance to othersYour ExperienceDegree with a major concentration in medical, biological, physical, health, pharmacy or other related scienceMinimum three year of experience in clinical research, in site activation and / or regulatory-related function within a CROCandidates must have experience of the regulatory process in the UK / and / or under EU-CTR (Poland, Denmark) to be considered for this role.Good knowledge of ICH GCP, relevant clinical research conduct guidance and country regulationsMultilingualism preferred; fluent in local language; working knowledge of EnglishWe love knowing that someone is going to have a better life because of the work we do.To 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.Worldwide 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 law.Seniority levelSeniority levelMid-Senior levelEmployment typeEmployment typeFull-timeJob functionJob functionLegalIndustriesResearch ServicesReferrals increase your chances of interviewing at Worldwide Clinical Trials by 2xSign in to set job alerts for "Regulatory Affairs Specialist" roles.Continue with Google Continue with GoogleContinue with Google Continue with GoogleWe're unlocking community knowledge in a new way.

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