{"id":809,"date":"2018-07-05T15:22:01","date_gmt":"2018-07-05T13:22:01","guid":{"rendered":"https:\/\/www.croalliance.com\/career-cv-submission\/"},"modified":"2025-09-19T13:00:33","modified_gmt":"2025-09-19T11:00:33","slug":"career-cv-submission","status":"publish","type":"page","link":"https:\/\/www.croalliance.com\/en\/career-cv-submission\/","title":{"rendered":"Career &#8211; CV submission"},"content":{"rendered":"<p>[vc_row][vc_column][vc_wp_custommenu nav_menu=&#8221;14&#8243;][vc_column_text]If you are looking for job opportunities or to establish a cooperation with us, feel free to submit your CV adding all the details you consider appropriate. Due to the high number of contacts we usually receive, we cannot guarantee a prompt reply to all of them, but be assured that every application is kept into consideration.[\/vc_column_text][vc_empty_space height=&#8221;20px&#8221;][\/vc_column][\/vc_row][vc_row css=&#8221;.vc_custom_1532446289607{margin-right: 6px !important;margin-left: 6px !important;padding-top: 12px !important;padding-right: 12px !important;padding-bottom: 12px !important;padding-left: 12px !important;background-color: #f6f6f6 !important;border-radius: 5px !important;}&#8221;][vc_column css=&#8221;.vc_custom_1532446249887{padding-top: 0px !important;}&#8221;][vc_column_text]<\/p>\n<h3>Pending positions<\/h3>\n<p style=\"text-align: justify;\">Here you can find the actual pending position(s) at <span style=\"color: #1565a2;\">CROss Alliance<\/span><span style=\"color: #1565a2;\">\u00ae<\/span>.<\/p>\n<p>Even if we do not have an open position in your role, we are always looking for potentially interesting and skilled figures working in the Pharma and CROs field, then if you deem it worthwhile, feel free to submit us your CV using the form below.<\/p>\n<p>Actual open positions:<\/p>\n<p><strong><span style=\"color: #1565a2;\">There are currently no vacancies available<\/span><\/strong>[\/vc_column_text][\/vc_column][\/vc_row][vc_row disable_element=&#8221;yes&#8221; css=&#8221;.vc_custom_1559310842919{margin-right: 6px !important;margin-left: 6px !important;padding-top: 12px !important;padding-right: 12px !important;padding-bottom: 12px !important;padding-left: 12px !important;background-color: #f6f6f6 !important;border-radius: 5px !important;}&#8221; el_id=&#8221;ARCHIVIO POSIZIONI &#8211; NASCOSTO&#8221;][vc_column css=&#8221;.vc_custom_1532446249887{padding-top: 0px !important;}&#8221;][vc_tta_accordion style=&#8221;flat&#8221; shape=&#8221;square&#8221; color=&#8221;white&#8221; active_section=&#8221;0&#8243; no_fill=&#8221;true&#8221; collapsible_all=&#8221;true&#8221;][vc_tta_section title=&#8221;Clinical Programmer and\/or Junior Biostatistician&#8221; tab_id=&#8221;1581343544073-4ab97101-0f95&#8243;][vc_column_text]In order to extend our team we are evaluating CVs of candidates, aged between 25 and 35 years old, for the position of <strong>Clinical Programmer and\/0r Junior Biostatistician<\/strong>.<\/p>\n<p>As part of the Biometry unit, the Clinical Programmer\/ Junior Biostatistician is responsible for applying and\/or providing expertise in statistical, programming, and data management methods in accordance with CROSS\u2019 policies and standard operating procedures (SOPs) to provide consistent high quality deliverables.<\/p>\n<p><span style=\"color: #1565a2;\"><em><span style=\"text-decoration: underline;\">BASIC QUALIFICATIONS<\/span> <\/em><\/span><\/p>\n<p>Work requires a minimum of a Master&#8217;s degree in (bio) statistics or related field and no relevant experience, or a bachelor\u2019s degree in (bio) statistics or related field and 1\/2 years relevant experience, or an equivalent combination or relevant education and\/or work experience. Master\u2019s degree is preferred.<\/p>\n<p><span style=\"text-decoration: underline;\"><span style=\"color: #1565a2; text-decoration: underline;\">PREFERRED QUALIFICATIONS<\/span><\/span><\/p>\n<ul>\n<li>Proficiency in programming using SAS and in the use of SAS Macro language<\/li>\n<\/ul>\n<ul>\n<li>Previous experience in pharmaceutical, biotech, CRO, Medical Device company with an emphasis on building data collection solutions desired<\/li>\n<li>Understanding of drug development process and data operations required for the reporting of clinical trial data (e.g. data review, study reports, regulatory submissions, safety updates, etc.)<\/li>\n<li>Understanding of regulatory requirements and relevant data standards; CDISC knowledge and experience are preferable<\/li>\n<li>Ability to program using SQL language is a plus<\/li>\n<li>Ability to work in a team environment and independently as needed<\/li>\n<li>Good organizational and analytical\/problem-solving skills<\/li>\n<li>Good written and verbal communication skills<\/li>\n<li>Ability to understand written English<\/li>\n<\/ul>\n<p><u><span style=\"color: #1565a2;\">RESPONSIBILITIES<\/span> <\/u><\/p>\n<ul>\n<li>Perform statistical analyses using SAS.<\/li>\n<li>Generate tabulation and analysis datasets according to CDISC SDTM and ADaM requirements and prepare annotated CRFs<\/li>\n<li>Provide statistical and data management input into the entire lifecycle of a clinical study, from the design to the clinical study report<\/li>\n<li>Write Statistical Analysis Plans, Data Management Plan, CRFs, and other study-specific documents for assigned projects<\/li>\n<li>Support to data management activities may include:\n<ul>\n<li>To prepare and validate databases<\/li>\n<li>To perform routinely data management activities (queries and data cleaning)<\/li>\n<\/ul>\n<\/li>\n<li>Participate in the development and maintenance of, and adhere to corporate policies and SOPs.<\/li>\n<\/ul>\n<p>The place of employment will be Mendrisio (Switzerland), in a young and dynamic team; home based or consultancy applications will not be taken into account. We offer a permanent contract (40 hours a week), flexible work schedules, innovative and challenging projects to deal with, training and career development opportunities.<\/p>\n<p>A feedback will not be provided to those applications that do not meet the above-mentioned requirements.[\/vc_column_text][\/vc_tta_section][vc_tta_section title=&#8221;Data Manager (DM)\/Clinical Programmer&#8221; tab_id=&#8221;1559310529353-9087bed1-7385&#8243;][vc_column_text]In order to extend our team we are evaluating CVs of candidates, aged between 25 and 35 years old, for the position of <strong>Data Manager (DM)\/Clinical Programmer<\/strong>.<\/p>\n<p>As part of the Biometry unit, the Data Manager (DM)\/Clinical Programmer position is responsible for creation and maintenance of database infrastructure for the collection of clinical data, for managing DM activities including but not limited to design, implementation and validation of databases, edit checks, import\/export of external data in accordance with CROSS\u2019 policies and standard operating procedures (SOPs) to provide consistent high quality deliverables.<\/p>\n<p><span style=\"text-decoration: underline;\"><strong>BASIC QUALIFICATIONS<\/strong> <\/span><\/p>\n<p>Bachelor&#8217;s degree in Computer Science, Mathematics\/Statistics, Life Science or equivalent, PL\/SQL, SAS, Java, relational database design and database programming skills. Equivalent combination of education and work experience will be also considered.<\/p>\n<p><strong><span style=\"text-decoration: underline;\">PREFERRED QUALIFICATIONS<\/span><\/strong><\/p>\n<ul>\n<li>Experience in Oracle<\/li>\n<li>Previous experience in pharmaceutical, biotech, CRO, Medical Device company with an emphasis on building data collection solutions desired<\/li>\n<li>Understanding of drug development process and data operations required for the reporting of clinical trial data (e.g. data review, study reports, regulatory submissions, safety updates, etc.)<\/li>\n<li>Understanding of regulatory requirements and relevant data standards; CDISC knowledge and experience are preferable<\/li>\n<li>Proficiency in the use of Microsoft Office Suite of tools<\/li>\n<li>Ability to work in a team environment and independently as needed<\/li>\n<li>Strategic thinking and decision-making capability<\/li>\n<li>Good organizational and analytical\/problem-solving skills<\/li>\n<li>Good written and verbal communication skills<\/li>\n<li>Ability to understand written English<\/li>\n<\/ul>\n<p><strong><u>RESPONSIBILITIES <\/u><\/strong><\/p>\n<ul>\n<li>Develop DB specifications and design and build DBs within Oracle Clinical application<\/li>\n<li>Program consistency and edit checks for clinical databases<\/li>\n<li>Develop Data Validation Plan (DVP)<\/li>\n<li>Develop Data Management Plan (DMP), maintains and adhere to DMP throughout lifecycle of study project<\/li>\n<li>Define and Perform MedDRA and\/or WHO coding<\/li>\n<li>Perform the quality control of clinical data<\/li>\n<li>May create annotated CRFs for clinical studies according to CDASH\/CDISC standards<\/li>\n<li>Develop Analytical Data Transfer Specification(s) (ADTS) between external data vendors<\/li>\n<li>Coordinate the archiving of study databases and related documents per SOPs<\/li>\n<li>Follow current SOPs. Further, provide input in identifying process improvements<\/li>\n<\/ul>\n<p>The place of employment will be Mendrisio (Switzerland), in a young and dynamic team; home based or consultancy applications will not be taken into account. We offer a permanent contract (40 hours a week), flexible work schedules, innovative and challenging projects to deal with, training and career development opportunities.<\/p>\n<p>A feedback will not be provided to those applications that do not meet the above-mentioned requirements.[\/vc_column_text][\/vc_tta_section][vc_tta_section title=&#8221;Data Manager&#8221; tab_id=&#8221;1547821332480-27e5bf2d-dd0c&#8221;][vc_column_text]<\/p>\n<p style=\"text-align: justify;\">Per ampiamento dell\u2019attuale organico, valutiamo Curriculum Vitae di giovani ambosessi di et\u00e0 compresa tra 30-40 anni, per una posizione di Data Manager.<\/p>\n<p style=\"text-align: justify;\">Saranno considerati fattori determinanti nella scelta:<\/p>\n<table style=\"height: 86px;\" border=\"0\" width=\"595\">\n<tbody>\n<tr>\n<td valign=\"top\">\u25aa<\/td>\n<td style=\"padding-left: 5px;\" valign=\"top\">laurea in ingegneria, fisica, matematica, statistica o equivalenti;<\/td>\n<\/tr>\n<tr>\n<td valign=\"top\">\u25aa<\/td>\n<td style=\"padding-left: 5px;\" valign=\"top\">buona conoscenza della lingua Inglese;<\/td>\n<\/tr>\n<tr>\n<td valign=\"top\">\u25aa<\/td>\n<td style=\"padding-left: 5px;\" valign=\"top\">conoscenza del linguaggio SQL;<\/td>\n<\/tr>\n<tr>\n<td valign=\"top\">\u25aa<\/td>\n<td style=\"padding-left: 5px;\" valign=\"top\">conoscenza dell&#8217;ambiente Oracle o altri database relazionali;<\/td>\n<\/tr>\n<tr>\n<td valign=\"top\">\u25aa<\/td>\n<td style=\"padding-left: 5px;\" valign=\"top\">conoscenza dei pacchetti SAS e relativa programmazione;<\/td>\n<\/tr>\n<tr>\n<td valign=\"top\">\u25aa<\/td>\n<td style=\"padding-left: 5px;\" valign=\"top\">precedente esperienza come Data Manager.<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p style=\"text-align: justify;\">La sede di lavoro sar\u00e0 Mendrisio (Svizzera), in un gruppo giovane e dinamico; non saranno prese in considerazione candidature &#8220;home based&#8221; o aventi carattere di consulenza. Si offre contratto a tempo indeterminato (40 ore settimanali), flessibilit\u00e0 sugli orari di ingresso ed uscita, necessit\u00e0 di fronteggiare progetti diversi con carattere di innovazione e possibilit\u00e0 di crescita e formazione.<\/p>\n<p>Segnaliamo che non sar\u00e0 fornita risposta alle candidature non rispondenti al profilo richiesto.<\/p>\n<p>[\/vc_column_text][\/vc_tta_section][vc_tta_section title=&#8221;Clinical Project Leader&#8221; tab_id=&#8221;1547821332504-93727183-3450&#8243;][vc_column_text]<\/p>\n<p style=\"text-align: justify;\">Per ampliamento dell\u2019attuale organico, valutiamo candidature per la posizione di Clinical Project Leader.<\/p>\n<p style=\"text-align: justify;\">Il potenziale candidato, sar\u00e0 responsabile della gestione di studi clinici dalla fase I alla fase III sia in Svizzera che in Paesi Europei, partendo ove necessario, dalla scrittura del Protocollo di studio, passando alla preparazione e sottomissione della documentazione per le approvazioni regolatorie fino alla verifica dei costi rispetto al budget previsto e lavorer\u00e0 a stretto contatto con gli sponsors e le diverse Units interne al gruppo CROss Alliance per l\u2019organizzazione, la conduzione ed il completamento dei trials in accordo alle time schedule prefissate.<\/p>\n<p style=\"text-align: justify;\">Il profilo ideale \u00e8 un laureato in materie scientifiche, con un&#8217;esperienza di almeno 5-6 anni nella ricerca clinica (di cui almeno 2 nel ruolo di Project Leader o Study Manager) presso aziende farmaceutiche o CROs, un\u2019approfondita conoscenza delle norme ICH-GCPs internazionali, buone doti di comunicazione, efficacia nella gestione e nel coordinamento di progetti, disponibilit\u00e0 al lavoro in team.<\/p>\n<p style=\"text-align: justify;\">La conoscenza fluente della lingua inglese \u00e8 un requisito fondamentale per il ruolo, sar\u00e0 considerato titolo preferenziale la conoscenza di una seconda lingua straniera.<\/p>\n<p style=\"text-align: justify;\">La ricerca \u00e8 aperta a candidati di ambo i sessi, preferibilmente di et\u00e0 compresa tra i 30 ed i 45 anni. Verr\u00e0 applicato il contratto di lavoro Svizzero in accordo al Codice delle Obbligazioni ed al momento non siamo interessati a posizioni home-based.<\/p>\n<p style=\"text-align: justify;\">Si richiede la disponibilit\u00e0 a brevi viaggi in Svizzera, Europa o Paesi extra-europei.<\/p>\n<p style=\"text-align: justify;\">Segnaliamo che non sar\u00e0 fornita risposta alle candidature non rispondenti al profilo richiesto.<\/p>\n<p>[\/vc_column_text][\/vc_tta_section][vc_tta_section title=&#8221;Junior Quality Assurance&#8221; tab_id=&#8221;1609587141261-a3c07517-277b&#8221;][vc_column_text]CROSS Research is looking for a young (25-35 years) <strong>Junior Quality Assurance<\/strong> to join its Quality Assurance team. This position will collaborate with the Quality Assurance Manager for establishing and ensuring the quality of clinical studies conducted by CROSS Research. Responsibilities include:<\/p>\n<ul>\n<li>Performing internal and external audits to clinical trials, documents and subcontractors and to ensure adherence to the GCP, applicable regulations, SOPs<\/li>\n<li>Supporting the management of the company Quality System and ensuring proper archiving of training documentation<\/li>\n<\/ul>\n<p>Candidates who satisfy the requirements listed below may be given preference in selection:<\/p>\n<ul>\n<li>Degree in Biology, Pharmacy, Chemistry or related disciplines<\/li>\n<li>Previous experience as Clinical Monitor, Quality Assurance or Regulator<\/li>\n<li>At least basic analytical experience to support audits to laboratories<\/li>\n<li>English fluency and independence in preparing technical documents and reports<\/li>\n<li>Good\/advanced computer use skills and at least basic knowledge of IT systems<\/li>\n<li>Availability to travelling<\/li>\n<\/ul>\n<p>Main place of work will be Mendrisio (Switzerland) but activities will be also performed in other company sites and own car is a requirement. This will be a full-time on-site employment (40 weekly hours). A challenging job in a small committed team is offered.<\/p>\n<p>Unsatisfactory candidates will not receive a reply to their application.<\/p>\n<p>[\/vc_column_text][\/vc_tta_section][\/vc_tta_accordion][\/vc_column][\/vc_row][vc_row][vc_column][vc_empty_space height=&#8221;20px&#8221;][vc_column_text]<\/p>\n<h3>Submit your CV<\/h3>\n<p>The information and CVs sent must contain a privacy disclosure and will be treated as confidential by CROss Alliance\u00ae.[\/vc_column_text][vc_empty_space height=&#8221;10px&#8221;]\n<div class=\"wpcf7 no-js\" id=\"wpcf7-f422-o1\" lang=\"it-IT\" dir=\"ltr\" data-wpcf7-id=\"422\">\n<div class=\"screen-reader-response\"><p role=\"status\" aria-live=\"polite\" aria-atomic=\"true\"><\/p> <ul><\/ul><\/div>\n<form action=\"\/en\/wp-json\/wp\/v2\/pages\/809#wpcf7-f422-o1\" method=\"post\" class=\"wpcf7-form init\" aria-label=\"Modulo di contatto\" enctype=\"multipart\/form-data\" novalidate=\"novalidate\" data-status=\"init\">\n<fieldset 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class=\"wpcf7-form-control wpcf7-text\" type=\"text\" name=\"honeypot-313\" value=\"\" size=\"40\" tabindex=\"-1\" autocomplete=\"off\" \/><\/span><span class=\"inline-label\">Full name <span class=\"req\">*<\/span><\/span><span class=\"wpcf7-form-control-wrap\" data-name=\"your-name\"><input size=\"40\" maxlength=\"400\" class=\"wpcf7-form-control wpcf7-text wpcf7-validates-as-required\" aria-required=\"true\" aria-invalid=\"false\" placeholder=\"enter your full name\" value=\"\" type=\"text\" name=\"your-name\" \/><\/span> <\/label><br \/>\n<label><span class=\"inline-label\">E-mail <span class=\"req\">*<\/span><\/span><span class=\"wpcf7-form-control-wrap\" data-name=\"your-email\"><input size=\"40\" maxlength=\"400\" class=\"wpcf7-form-control wpcf7-email wpcf7-validates-as-required wpcf7-text wpcf7-validates-as-email\" aria-required=\"true\" aria-invalid=\"false\" placeholder=\"enter a valid e-mail address\" value=\"\" type=\"email\" name=\"your-email\" \/><\/span> <\/label><br \/>\n<label><span class=\"inline-label\">Position <span class=\"req\">*<\/span><\/span><span class=\"wpcf7-form-control-wrap\" data-name=\"your-position\"><select class=\"wpcf7-form-control wpcf7-select wpcf7-validates-as-required\" aria-required=\"true\" aria-invalid=\"false\" name=\"your-position\"><option value=\"\">&#8212;Seleziona un&#039;opzione&#8212;<\/option><option value=\"General unpositioned role\">General unpositioned role<\/option><\/select><\/span> <\/label><br \/>\n<label><span class=\"inline-label\">Subject <span class=\"req\">*<\/span><\/span><span class=\"wpcf7-form-control-wrap\" data-name=\"your-subject\"><input size=\"40\" maxlength=\"400\" class=\"wpcf7-form-control wpcf7-text wpcf7-validates-as-required\" aria-required=\"true\" aria-invalid=\"false\" placeholder=\"subject of the message\" value=\"\" type=\"text\" name=\"your-subject\" \/><\/span> <\/label><br \/>\n<label><span class=\"inline-label\">Text <span class=\"req\">*<\/span><\/span><span class=\"wpcf7-form-control-wrap\" data-name=\"your-message\"><textarea cols=\"40\" rows=\"10\" maxlength=\"2000\" class=\"wpcf7-form-control wpcf7-textarea wpcf7-validates-as-required\" aria-required=\"true\" aria-invalid=\"false\" placeholder=\"write your message\" name=\"your-message\"><\/textarea><\/span><\/label><br \/>\n<label><span class=\"inline-label\">CV attachment<\/span><span class=\"wpcf7-form-control-wrap\" data-name=\"file-cv\"><input size=\"40\" class=\"wpcf7-form-control wpcf7-file\" accept=\".pdf,.txt,.doc,.docx,.jpg,.png,.jpeg\" aria-invalid=\"false\" type=\"file\" name=\"file-cv\" \/><\/span><\/label><br \/>\n<label class=\"accept\"><span class=\"wpcf7-form-control-wrap\" data-name=\"acceptance-cross\"><span class=\"wpcf7-form-control wpcf7-acceptance\"><span class=\"wpcf7-list-item\"><input type=\"checkbox\" name=\"acceptance-cross\" value=\"1\" aria-invalid=\"false\" \/><\/span><\/span><\/span> <span class=\"inline-acceptance\"> <span class=\"req\">*<\/span> I 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