{"id":4089,"date":"2022-11-08T18:58:42","date_gmt":"2022-11-08T10:58:42","guid":{"rendered":"https:\/\/credevo.com\/s\/?page_id=4089"},"modified":"2025-07-31T23:10:51","modified_gmt":"2025-07-31T15:10:51","slug":"clinical-trial-lead","status":"publish","type":"page","link":"https:\/\/credevo.com\/s\/clinical-trial-lead\/","title":{"rendered":"Clinical Trial Lead \/ Clinical Trial Manager"},"content":{"rendered":"\n

Job Description<\/h3>\n\n\n\n
Job Title<\/td>Clinical Trial Lead \/ Clinical Trial Manager<\/td><\/tr>
Reports to<\/td>CEO<\/td><\/tr>
Department<\/td>Business Development<\/td><\/tr>
Location<\/td>Remote<\/td><\/tr>
Supervises <\/td> All activities
related to various projects and general departmental activities.<\/td><\/tr>
Job Type<\/td>Contract<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n

Company Overview <\/h3>\n\n\n\n

Credevo<\/a> is a global consulting organization supporting healthcare product development from clinical development to commercialization. Credevo provides strategic support in areas such as regulatory, clinical development, licensing (out-\/in-), and feasibility support, for products including pharmaceuticals, biologics, nutraceuticals, and medical devices.<\/p>\n\n\n\n

Position Overview <\/h3>\n\n\n\n

This is a remote position reporting to the company management. The role will be clinical trial
lead \/ Clinical Trial Manager who can effectively lead, supervise, and manage all activities
related to various projects and general departmental activities.<\/p>\n\n\n\n

Experience:<\/h3>\n\n\n\n

Sites and investigators relations: Develop, consolidate, expand, and manage
Credevo\u2019s relationship with its current global network of sites and investigators by<\/p>\n\n\n\n

At least 5 years of overall clinical trial experience- out of which
a. at least 2 years should be in on-site visits based trial monitoring, in a minimum of
2 trial projects and
b. at least 1 year should be as clinical trial lead or clinical trial manager across a
minimum of 2 projects<\/p>\n\n\n\n

Candidates with significant experience in building and maintaining site- \/ investigatorrelations will be preferred.<\/p>\n\n\n\n

Experience in sponsor facing roles will be an added advantage.
Responsibilities:
Essential duties and responsibilities include but are not limited to the following:<\/p>\n\n\n\n

Client communication<\/strong>: Communicate and coordinate with customers to understand
their needs for clinical trials, evaluate product details, business needs, and customer
requirements to
a. identify the study rationale,
b. identify key geographic regions for the trial,
c. prepare a strategic plan for the trial and advise on the way forward<\/p>\n\n\n\n

Trial management:<\/strong> Lead, supervise, and manage clinical trial projects across sites in
Asia-Pac, the US, and India locations, including but not limited to
a. Development of internal and external trial teams,
b. Study document development and finalization
c. Feasibility assessment and site selection
d. Other study start-up activities, such as RA and ethics submission
e. Selection and management of relations with sites, investigators, and vendors
f. Clinical operations, including monitoring and site management leading to
completion of data entry and data management activities up to database lock<\/p>\n\n\n\n

    \n
  1. Sites and investigators relations:<\/strong> Develop, consolidate, expand, and manage
    Credevo\u2019s relationship with its current global network of sites and investigators by:<\/li>\n<\/ol>\n\n\n\n

    a. Strengthening connectivity to and communications with more than 150,000
    investigators across the world
    b. Building systems and processes to evaluate clinical trial feasibility
    c. Identifying key needs of sites and investigators in Credevo\u2019s network
    d. Developing solutions to support investigators<\/p>\n\n\n\n

    Management support<\/strong>: Work with company management and provide required support
    in all clinical trial-related areas, including but not limited to
    a. Development and implementation of key tools, systems, and study processes
    such as SOPs, and quality control measures.
    b. Maintaining comprehensive and up-to-date knowledge of relevant regulations,
    guidelines, and best practices in clinical research.
    c. Undertaking key initiatives to improve the current status of clinical research and
    other management drives in organizational development
    d. Ensuring timely reporting to the management team and relevant stakeholders.<\/p>\n\n\n\n

    Qualifications:<\/strong><\/p>\n\n\n\n

      \n
    1. At least a graduate, preferably in life sciences, healthcare, pharmaceutical or medical
      streams.<\/li>\n\n\n\n
    2. Trained and expert in ICH Good Clinical Practice (GCP) and regulatory processes.<\/li>\n<\/ol>\n\n\n\n

      Skills & Abilities:<\/strong><\/p>\n\n\n\n

        \n
      1. Trained and ready to work in a global environment and flexible to work across multiple
        time zones.<\/li>\n\n\n\n
      2. Advanced knowledge of working in Google Suite \/ Microsoft Office Suite (Word, Excel,
        SharePoint, Teams, etc.) as well as electronic documentation systems.<\/li>\n\n\n\n
      3. Demonstrated ability to lead teams and prepare organizational strategies, especially for
        clinical trial management<\/li>\n\n\n\n
      4. Quick learner and work well without constant supervision.<\/li>\n\n\n\n
      5. Ability to understand and comprehend the needs of the work and cooperate well.<\/li>\n<\/ol>\n\n\n\n

        Language Proficiency:<\/strong><\/p>\n\n\n\n

          \n
        1. Expert in written communication skills in the English language \u2013 This should be
          demonstrated by prior work and on-the-spot tests (during the selection process).<\/li>\n\n\n\n
        2. Good English speaking skills with the ability to understand different international
          accents are also required.<\/li>\n<\/ol>\n\n\n\n
          \n
          Apply Using Gmail \/ Google Account<\/a><\/div>\n<\/div>\n\n\n\n

          IMPORTANT:<\/em><\/strong> You will need to login to your gmail \/ google account for authentication to apply.<\/em><\/p>\n","protected":false},"excerpt":{"rendered":"

          Job Description Job Title Clinical Trial Lead \/ Clinical Trial Manager Reports to CEO Department Business Development Location Remote Supervises  All activitiesrelated to various projects and general departmental activities. Job Type Contract Company Overview Credevo is a global consulting organization supporting healthcare product development from clinical development to commercialization. Credevo provides strategic support in areas […]<\/p>\n","protected":false},"author":2,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":""},"class_list":["post-4089","page","type-page","status-publish","hentry"],"acf":[],"yoast_head":"\nClinical Trial Lead \/ Clinical Trial Manager<\/title>\n<meta name=\"description\" content=\"Join Credevo as a Clinical Trial Lead\/Manager (Remote, Contract) to oversee global clinical trial operations, site relations etc.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/credevo.com\/s\/clinical-trial-lead\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Clinical Trial Lead \/ Clinical Trial Manager\" \/>\n<meta property=\"og:description\" content=\"Join Credevo as a Clinical Trial Lead\/Manager (Remote, Contract) to oversee global clinical trial operations, site relations etc.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/credevo.com\/s\/clinical-trial-lead\/\" \/>\n<meta property=\"og:site_name\" content=\"Credevo\" \/>\n<meta property=\"article:publisher\" content=\"https:\/\/www.facebook.com\/credevo\" \/>\n<meta property=\"article:modified_time\" content=\"2025-07-31T15:10:51+00:00\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:site\" content=\"@gocredevo\" \/>\n<meta name=\"twitter:label1\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data1\" content=\"3 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\/\/credevo.com\/s\/clinical-trial-lead\/\",\"url\":\"https:\/\/credevo.com\/s\/clinical-trial-lead\/\",\"name\":\"Clinical Trial Lead \/ Clinical Trial Manager\",\"isPartOf\":{\"@id\":\"https:\/\/credevo.com\/s\/#website\"},\"datePublished\":\"2022-11-08T10:58:42+00:00\",\"dateModified\":\"2025-07-31T15:10:51+00:00\",\"description\":\"Join Credevo as a Clinical Trial Lead\/Manager (Remote, Contract) to oversee global clinical trial operations, site relations etc.\",\"breadcrumb\":{\"@id\":\"https:\/\/credevo.com\/s\/clinical-trial-lead\/#breadcrumb\"},\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\/\/credevo.com\/s\/clinical-trial-lead\/\"]}]},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\/\/credevo.com\/s\/clinical-trial-lead\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Services\",\"item\":\"https:\/\/credevo.com\/s\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"Clinical Trial Lead \/ Clinical Trial Manager\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\/\/credevo.com\/s\/#website\",\"url\":\"https:\/\/credevo.com\/s\/\",\"name\":\"Credevo\",\"description\":\"Healthcare Product Development from Clinical Development to Commercialization\",\"publisher\":{\"@id\":\"https:\/\/credevo.com\/s\/#organization\"},\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\/\/credevo.com\/s\/?s={search_term_string}\"},\"query-input\":{\"@type\":\"PropertyValueSpecification\",\"valueRequired\":true,\"valueName\":\"search_term_string\"}}],\"inLanguage\":\"en-US\"},{\"@type\":\"Organization\",\"@id\":\"https:\/\/credevo.com\/s\/#organization\",\"name\":\"Credevo Pte. 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